Hostname: page-component-7c8c6479df-ph5wq Total loading time: 0 Render date: 2024-03-29T03:52:24.043Z Has data issue: false hasContentIssue false

Micronutrient intakes and potential inadequacies of community-dwelling older adults: a systematic review

Published online by Cambridge University Press:  30 March 2015

Sovianne ter Borg*
Affiliation:
Nutricia Research, Nutricia Advanced Medical Nutrition, Uppsalalaan 12, PO Box 80141, 3508TC, Utrecht, The Netherlands
Sjors Verlaan
Affiliation:
Nutricia Research, Nutricia Advanced Medical Nutrition, Uppsalalaan 12, PO Box 80141, 3508TC, Utrecht, The Netherlands
Jaimie Hemsworth
Affiliation:
Nutricia Research, Nutricia Advanced Medical Nutrition, Uppsalalaan 12, PO Box 80141, 3508TC, Utrecht, The Netherlands
Donja M. Mijnarends
Affiliation:
Department of Health Services Research, School CAPHRI, Maastricht University, Maastricht, The Netherlands
Jos M. G. A. Schols
Affiliation:
Department of Health Services Research, School CAPHRI, Maastricht University, Maastricht, The Netherlands Department of Family Medicine, School CAPHRI, Maastricht University, Maastricht, The Netherlands
Yvette C. Luiking
Affiliation:
Nutricia Research, Nutricia Advanced Medical Nutrition, Uppsalalaan 12, PO Box 80141, 3508TC, Utrecht, The Netherlands
Lisette C. P. G. M. de Groot
Affiliation:
Division of Human Nutrition, Wageningen University, Wageningen, The Netherlands
*
*Corresponding author: S. ter Borg, email sovianne.terborg@nutricia.com
Rights & Permissions [Opens in a new window]

Abstract

Micronutrient deficiencies and low dietary intakes among community-dwelling older adults are associated with functional decline, frailty and difficulties with independent living. As such, studies that seek to understand the types and magnitude of potential dietary inadequacies might be beneficial for guiding future interventions. We carried out a systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement. Observational cohort and longitudinal studies presenting the habitual dietary intakes of older adults ( ≥ 65 years) were included. Sex-specific mean (and standard deviation) habitual micronutrient intakes were extracted from each article to calculate the percentage of older people who were at risk for inadequate micronutrient intakes using the estimated average requirement (EAR) cut-point method. The percentage at risk for inadequate micronutrient intakes from habitual dietary intakes was calculated for twenty micronutrients. A total of thirty-seven articles were included in the pooled systematic analysis. Of the twenty nutrients analysed, six were considered a possible public health concern: vitamin D, thiamin, riboflavin, Ca, Mg and Se. The extent to which these apparent inadequacies are relevant depends on dynamic factors, including absorption and utilisation, vitamin and mineral supplement use, dietary assessment methods and the selection of the reference value. In light of these considerations, the present review provides insight into the type and magnitude of vitamin and mineral inadequacies.

Type
Review Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Authors 2015

One of the most profound current shifts in demographics is the rapidly increasing population of older adults. The world population of people older than 60 years has gone from slightly more than 100 million in 1950 to more than 800 million in 2011/2012, and it is expected to exceed 2 billion by the year 2050( 1 ). Within the older population itself, there is an annual increase of 4 % in the number of people older than 80 years( 1 ). Ageing is often seen as being synonymous with frailty and disability. However, there is significant variation in age-related functional changes in older adults and, as such, widely varying dietary and nutritional needs. In the Netherlands, for example, there is a high prevalence of undernutrition among community-dwelling older adults( Reference Schilp, Kruizenga and Wijnhoven 2 ). Variation exists in the nutritional needs of this population, as about of the general population 11 % older than 65 years are undernourished, and this is tripled to 35 % among a population of older adults receiving home care( Reference Schilp, Kruizenga and Wijnhoven 2 ). The aetiology of undernutrition among older adults is complex and related to intrinsic factors, such as changes in the absorption and utilisation of nutrients and chronic disease, as well as extrinsic factors, such as poor appetite, interactions with medications, reduced enjoyment/skill in meal preparation and consumption( Reference van Staveren and de Groot 3 ) and changes in the types and amounts of foods consumed( Reference Houston, Stevens and Cai 4 ). Multiple micronutrient inadequacies among older community-dwelling adults are well described in the literature( Reference de Groot, van den Broek and van Staveren 5 , Reference Marshall, Stumbo and Warren 6 ). Micronutrient inadequacies appear to worsen with increasing age( Reference Zhu, Devine and Suleska 7 ), which is associated with decreased energy intakes( Reference de Groot, van den Broek and van Staveren 5 ). There is a compound effect of micronutrient deficiencies in which an increasing number of deficient nutrients is associated with an increased incidence of frailty (hazard ratio 1·12, 95 % CI 1·03, 1·22, P= 0·01)( Reference Semba, Bartali and Zhou 8 ). Micronutrient deficiencies pose a considerable threat to independence and longevity, because they are related to several adverse functional outcomes( Reference Inzitari, Doets and Bartali 9 ).

To our knowledge, there has not been any other systematic review of micronutrient intakes among community-dwelling older adults in developed Western countries in the literature. In light of the growing presence of this segment of the population, as well as changing and diverse nutritional needs, the present systematic review fills an important knowledge gap.

The objectives of the present systematic review were (1) to describe the habitual dietary intake of micronutrients and (2) to describe the percentage of the population at risk for inadequate intakes of micronutrients among community-dwelling older adults in Western countries.

Methods

The present systematic review followed the reporting checklist as part of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statement( Reference Moher, Liberati and Tetzlaff 10 ).

Search strategy and selection of studies

The electronic databases PubMed and EMBASE were searched between the following dates: 1950 to 6 October 2011 and 1993 to 6 October 2011. The review was later updated and the same search terms were used in both databases for a search between October 2011 and 31 December 2013. The following search string was used for the searches: (‘elderly’ OR ‘geriatric’ OR ‘older adults’ OR ‘older people’ OR ‘senior’ OR ‘older person’ OR ‘aging’) AND (‘nutritional status’ OR ‘nutrient deficiency’ OR ‘nutrient deficiencies’ OR ‘nutrient deficient’ OR ‘nutrient intake’ OR ‘nutritional intake’ OR ‘food intake’ OR ‘dietary intake’ OR ‘dietary adequacy’ OR ‘nutrition assessment’ OR ‘diet records’) AND (‘population-based study’ OR ‘longitudinal study’ OR ‘epidemiologic study’ OR ‘cohort study’ OR ‘prospective study’ OR ‘cross-sectional study’ OR ‘population-based design’ OR ‘longitudinal design’ OR ‘epidemiologic design’ OR ‘cohort design’ OR ‘prospective design’ OR ‘cross-sectional design’). All possible articles were merged into one database, and duplicate records were removed. Additional articles were identified by checking the reference lists of the relevant articles, in addition to searching for national dietary/food consumption surveys. The titles and abstracts of all studies were scanned independently by two reviewers (S. t. B. and D. M. M. during the first search period and S. t. B. and J. H. during the second search period). Studies were considered eligible if they: contained nutrient intake data, were not based on a randomised controlled trial or nutrition intervention, had participants with a mean age of ≥ 65 years and had data originating from Western countries (Europe, North America, Australia or New Zealand).

Full-text articles were then assessed (by S. t. B. and J. H.) based on these selection criteria as well as the following additional criteria: if they studied community-dwelling older adults, if they had non-adjusted data( Reference Bermudez, Falcon and Tucker 11 , Reference Velho, Marques-Vidal and Baptista 12 ) and if micronutrient intake data were stated. Community-dwelling older adults were defined as those living at home, living in private households, independently living, free living or being non-institutionalised. Studies stating only the overall (men and women combined) nutrient intake data were excluded because of the separate nutrient requirements for men and women. A third reviewer (Y. C. L.) was consulted if it was unclear whether or not the article met the inclusion criteria.

Quality assessment and data extraction

The quality of the included articles and the potential bias on the outcome was assessed based on a scale that combined the Newcastle–Ottawa quality assessment scale( Reference Wells, Shea and O'Connell 13 ) and the Cochrane coding manual for cohort studies( 14 ), using the criteria applicable for observational studies. Table 1 summarises the criteria and point assignment for the quality assessment. Summary quality scores of 0–2, 3–4 and 5 were rated as low, moderate and high, respectively. Studies were then categorised according to these ratings. Nutrient intake data from national food consumption surveys were extracted from the European Nutrition and Health Report( Reference Elmadfa, Meyer and Nowak 15 ) and the European Food Safety Authority 2012 report( 16 ). The original articles were, however, used to assess study quality, because the reports did not contain detailed information on the quality criteria. The following study characteristics were extracted (Table 2): sample size, age range, dietary assessment method and country of origin. For each of the included studies, the mean (and standard deviation) ‘habitual’ dietary intakes of micronutrients were extracted by sex and age category. Articles were checked for reporting on potential supplement intake (yes/no) and whether supplement intake was included in their analyses (Table 2). Where data were presented as being stratified by sex and by an additional category (e.g. cognitive status), the pooled mean and standard deviation were calculated by sex group. To compare nutrient intake data with nutritional reference values, data were extracted by sex and subgroup (i.e. age category, country and year of data collection). In cases of longitudinal studies, baseline data were used, or when baseline data were not provided in the article, the follow-up measurement data were used.

Table 1 Overview of the study quality assessment*

EURRECA, European Micronutrient Recommendations Aligned.

* Summary score: 0–2 points = low quality, 3–4 points = moderate quality, 5 points = high quality.

Table 2 Characteristics of the included studies, assessing nutrient intake in community-dwelling older adults

DR, dietary record; 24HR, 24 h dietary recall; DH, dietary history; NA, not applicable because data was not available; 48HR, 48 h dietary recall; USDA, US Department of Agriculture.

* Data were published with and without supplement intake included; habitual intake (without supplement intake) was used in the analysis for the present systematic review.

Data analysis

All analyses were done in IBM SPSS Statistics version 19.0 (2010, IBM Company). Graphics were done in GraphPad Prism version 6.00 for Windows (GraphPad Software).

Pooled means and standard deviations were calculated by sex for each nutrient. We performed a sensitivity analysis using a one-way ANOVA comparing the mean nutrient intakes in each study-quality subgroup with an ad hoc least significant difference test to assess between-group differences. Significant differences in micronutrient intakes by quality subgroup were defined as P< 0·05.

Micronutrient estimated average requirements (EAR) from the Nordic Nutrition Recommendations( 17 ) were used for most nutrients. The Institute of Medicine's EAR was used for Mg( 18 ), because it was not provided in the Nordic Nutrition Recommendation. In addition, the updated Institute of Medicine's EAR for vitamin D and Ca( Reference Ross, Manson and Abrams 19 ) were used. Adequate intake values were used for K and Na, because there are not yet EAR for these nutrients for the older age group( 20 ). Sex-specific and age-specific (older than 60 years) recommendations were used if stated. The EAR cut-point method( 21 ) was used to calculate the prevalence of inadequate intakes for each nutrient. This method assumes normal distribution of both the population intakes and the recommendation. Because the EAR is a recommendation that meets the needs of at least 50 % of the population, the mean and standard deviation of the intakes (when normally distributed) can be used to calculate the percentage of the population that are falling below the recommendation and as such are at risk for inadequacy. Nutrients were considered to be a potential concern when the prevalence of inadequate intakes was equal to or above 30 % of the population for both men and women. For K and Na, the mean intake was compared with the adequate intake in order to make a qualitative comparison. If the intake was above the adequate intake, a low prevalence of inadequacy was assumed. If the intake was below the adequate intake, the inadequacy could not be determined.

Results

A total of 966 articles were identified as potentially relevant from the two searches (Fig. 1). This resulted in thirty-seven separate articles from more than 28 000 (57 % female) community-dwelling older adults in twenty different Western countries (Table 2). There was a range in individual study quality – twenty-one of the thirty-seven studies were of moderate quality, six were of low quality, nine were of high quality, and one article's quality could not be assessed due to insufficient information (Table 2; see online supplementary Table S1 for full quality assessment). The results of the sensitivity analysis showed no significant differences (P>0·05) between mean nutrient intakes in each of the three quality subgroups. The cut-point analysis was, therefore, derived from the means and standard deviations of the full sample (see online supplementary Tables S2–S5 for the dietary intake data from each study).

Fig. 1 Systematic reviews and meta-analyses (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) flowchart of article selection and inclusion.

Habitual vitamin intakes and percentage at risk

The mean dietary intakes of ten vitamins (vitamin A, thiamin (B1), riboflavin (B2), niacin (B3), vitamins B6 and B12, folate and vitamins C, D and E) by both men and women are summarised in Table 3. The percentage of the population at risk for inadequate intakes of vitamins from food alone was greater than 30 % for both men and women for three of the ten analysed vitamins: thiamin, riboflavin and vitamin D (Fig. 2). Half of the male population was at risk for inadequate intake of thiamin as compared to the female population, where one-third (39 %) was at risk for an inadequacy. Fewer men and women were at risk for riboflavin inadequacy, with 41 and 31 % for men and women, respectively, having inadequate intakes. Most men and women were at risk for inadequate dietary intakes of vitamin D (84 and 91 % for men and women, respectively). Vitamins that showed lower rates of inadequacy but that could also be a potential dietary concern include: vitamin A (29 and 26 % for men and women, respectively), vitamin B6 (31 and 24 %), folate (29 and 35 %), vitamin C (29 and 23 %) and vitamin E (26 and 21 %).

Table 3 Daily vitamin intake and percentage of inadequate intakes among older adults (Mean values and standard deviations; percentages and 95 % confidence intervals)

EAR, estimated average requirement; M, men; RE, retinol equivalent; W, women; TE, tocopherol equivalent.

* Mean percentage of inadequate intakes, calculated with the EAR cut-point method.

Fig. 2 Mean (95 % CI) percentage of men () and women () at risk for inadequate intake of vitamins.

Habitual mineral intakes and percentage at risk

The mean dietary intakes of ten minerals (Ca, Cu, I, Fe, Mg, P, K, Se, Na and Zn) by both men and women are summarised in Table 4.

Table 4 Daily mineral intake and percentage of inadequate intakes among older adults (Mean values and standard deviations; percentages and 95 % confidence intervals)

EAR, estimated average requirement; M, men; W, women; NA, not applicable.

* Mean percentage of inadequate intakes, calculated with the EAR cut-point method.

Adequate intake, thus unable to apply EAR cut-point method.

Mean intake was below the adequate intake; no conclusion can be made about inadequacy.

§ Mean intake is above adequate intake; a low prevalence of inadequacy is assumed.

The percentage of the population at risk for inadequate dietary intakes of minerals from food alone was equal to or greater than 30 % for both men and women for three of the analysed minerals: Ca, Mg and Se. Fig. 3 shows the percentage at risk of inadequacy; two nutrients show a clear ‘higher’ risk for inadequacy than the other nutrients. Nearly two-thirds (65 %) of the population of men had inadequate intakes of Ca, and three-quarters (73 %) of the population of women were at risk for inadequacy for Ca. Almost three-quarters (73 %) of the population of men and nearly half (41 %) of the population of women were at risk for inadequate intakes of Mg. For both men and women, 30 % were at risk of Se inadequacy. Finally, iodine showed a potential risk for inadequate intakes, with 20 % of men and 26 % of women being at risk.

Fig. 3 Mean (95 % CI) percentage of men () and women () at risk for inadequate intake of minerals.

Discussion

The present systematic review identified six nutrients of potential concern as a result of a high prevalence of inadequacies – thiamin, riboflavin, vitamin D, Ca, Mg and Se. The results from the present systematic review support previous reports of low micronutrient adequacy in older adult diets in Europe( Reference Mensink, Fletcher and Gurinovic 22 , Reference Roman Vinas, Ribas Barba and Ngo 23 ). Potential vitamin D, Ca, Mg and Se inadequacies were also identified in younger adult populations (aged 19 years and older)( 24 , Reference van Rossum, Fransen and Verkaik-Kloosterman 25 ). This suggests that these inadequacies might not be confined to the older adult population.

Whether these low micronutrient intakes are of true public health concern and the other nutrients are not of public health concern depends on several factors. In older adults, the picture of nutritional status is not complete without also considering nutrient absorption, including sun exposure in the case of vitamin D, and utilisation as assessed by biochemical status, micronutrient supplementation use and potential differences in the nutrient requirements/recommendations upon which the percentage at risk calculation is based. Therefore, the results of the present systematic review are to be interpreted in light of these dynamic factors.

Nutrient absorption, utilisation and biochemical status

Vitamin D

A high proportion of the population has low intakes of vitamin D, because dietary sources are rare and are limited to fatty fish and, in some cases, dairy products( Reference Brouwer-Brolsma 26 ). Most of the vitamin D we use is delivered through skin synthesis and/or dietary supplement intake( Reference Brock, Ke and Tseng 27 ). In addition, fortified foods can contribute to vitamin D intake. Nevertheless, serum concentrations of 25-hydroxyvitamin D (25(OH)D) remain deficient ( < 50 nmol/l) in 40–100 % of senior populations globally( Reference Brouwer-Brolsma 26 , Reference Mithal, Wahl and Bonjour 28 ). Vitamin D deficiencies have been related to fractures, falls and low physical performance and potentially also to age-related cognitive decline( Reference Brouwer-Brolsma 26 ). Among the thirty-eight studies we reviewed, three published 25(OH)D levels for the same participants for the same period of dietary intake. The mean 25(OH)D level in these studies was 56·2 (sd 14·0) nmol/l among men and 51·7 (sd 9·6) nmol/l among women. Assuming normal distribution, this suggests that approximately half of the population in these studies is deficient in vitamin D, which agrees with the estimated range of deficiencies among older adults( Reference Brouwer-Brolsma 26 ). A study of community-dwelling older adults in Canada showed that higher intakes of vitamin D (both dietary and supplementary) result in a higher adequacy of 25(OH)D levels( Reference Ginter, Krithika and Gozdzik 29 ). The sample was stratified by a combined dietary and supplementary intake of 20 μg/d, where 34 % of the sample was below and 66 % of the sample was above this intake level. Of the sample that had intake below this level, 35 % had deficient 25(OH)D levels of < 50 nmol/l, and of those who had intake above this level, only 2 % had deficient 25(OH)D levels. Of the adequate consumers, 73 % had sufficient 25(OH)D levels ( ≥ 75 nmol/l). Therefore, the habitual intake of vitamin D observed in the present study is alarming considering the worldwide prevalence of vitamin D deficiencies. Higher dietary and supplementary intakes of vitamin D result in the reversal of vitamin D deficiencies and an increase in serum 25(OH)D concentrations among community-dwelling older adults( Reference Chung, Balk and Brendel 30 ). As such, this is a worthwhile intervention for preventing and reversing vitamin D deficiencies.

Calcium and magnesium

Considering the high prevalence of dietary inadequacy of Ca and Mg, measures of actual status would be useful to interpret whether these nutrients pose true health concerns at a population level. However, biomarkers for Ca and Mg are generally thought to be problematic because they have no specific useful measurement technique( Reference Witkowski, Hubert and Mazur 31 ). The functional outcome of Ca intake is often bone density, where higher intakes of Ca (>500 mg/d) plus vitamin D3 are associated with a higher bone density( Reference Chung, Balk and Brendel 30 ) and thus a decreased risk of fractures. However, Ca absorption is dependent on vitamin D intake, because vitamin D facilitates the intestinal absorption of Ca( Reference Heaney 32 ). Mg is also thought to be involved in the development of healthy bones, and it could play a role in muscle mass development( Reference Scott, Blizzard and Fell 33 ) and muscle performance in older adults( Reference Dominguez, Barbagallo and Lauretani 34 ).

B vitamins

The prevalence of inadequate intakes of thiamin (B1) and riboflavin (B2) were of concern for both men and women. Although subclinical deficiencies of these nutrients have been reported and have been linked with cognitive outcomes( 35 ), there does not appear to be a large public health concern about this level of thiamin and riboflavin dietary intakes.

The prevalence of inadequate vitamin B6 intake among the present pooled population was on the threshold of being a concern, because 31 % of men and 24 % of women were at risk of having inadequate intakes. Although it is an essential nutrient, vitamin B6 is not thought to be a typical nutrient of concern because it is fairly ubiquitous in Western diets( 36 ). However, vitamin B12, which is apparently adequate through habitual intakes, is frequently deficient in the blood values of older adults( Reference Allen 37 ). Malabsorption of vitamin B12 is the primary cause of the low vitamin B12 status among older adults, because atrophy of the gastric folds impairs gastric acid production, which reduces the activity of intrinsic factors that are essential for the absorption of vitamin B12 ( Reference Allen 37 ). Even high intakes of vitamin B12 from dietary and supplementary sources have a plateau effect in increasing serum concentrations because there is less efficient absorption with higher intakes( Reference Bor, Lydeking-Olsen and Moller 38 ). Low levels of vitamin B12 have been linked with an increased risk of fractures( Reference van Wijngaarden, Doets and Szczecinska 39 ), and less robust evidence exists for a relationship between vitamin B12 status and cognitive function( Reference Doets, van Wijngaarden and Szczecinska 40 ). Homocysteine, an α-amino acid that becomes elevated in plasma when vitamin B6, vitamin B12 or folate levels are suboptimal, is raised in 30–50 % of populations of adults aged 60 years or older (reviewed in van Wijngaarden et al. ( Reference van Wijngaarden, Doets and Szczecinska 39 )). Elevated homocysteine levels are significantly associated with bone fracture risk( Reference van Wijngaarden, Doets and Szczecinska 39 ), are an independent risk factor in CVD( Reference Jacobsen 41 , Reference Refsum, Nurk and Smith 42 ) and are implicated in the reduced physical function of older adults( Reference van Schoor, Swart and Pluijm 43 ). There is evidence that vitamin B12, folate and perhaps vitamin B6 play a role in reducing homocysteine levels( 44 ).

Antioxidants (selenium and vitamins A, C and E)

In the present pooled population, a high proportion of inadequate intakes of Se was observed in both men and women. Clinical deficiencies are rare, but higher serum Se concentrations have been associated with protective effects against cancer and anaemia( Reference Semba, Ricks and Ferrucci 45 , Reference Thomson 46 ). The hypothesised mechanism for anaemia protection is through Se's antioxidant activity, which prevents erythrocyte oxidation and damage( Reference Semba, Ricks and Ferrucci 45 ). However, the link between Se intake and serum Se concentrations, especially among elderly populations, is not well understood( Reference Semba, Ricks and Ferrucci 45 ). One of the pathways that leads to frailty and disability among older adults is oxidative stress( Reference Semba, Bartali and Zhou 8 ). Serum carotenoids and serum Se were both significantly negatively related to frailty in an observational study in elderly women in the USA( Reference Semba, Ricks and Ferrucci 45 ). Serum α-tocopherol also showed a trend between low serum levels and frailty (P= 0·06). This suggests, at least among the present group of women, that antioxidants play a strong role in the development of frailty and disability, independent of other background factors, such as smoking, educational attainment and chronic disease. We observed a borderline (20–30 %) high prevalence of vitamin A, C and E dietary inadequacies. Although serum markers are questioned for their reliability concerning dietary intake( Reference van Kappel, Steghens and Zeleniuch-Jacquotte 47 ), serum markers of antioxidants are linked with frailty and disability. The present results suggest that this pooled population of older adults could have important dietary shortages of antioxidants.

Vitamin and mineral supplement intake and adequacy of intakes

Habitual dietary intakes of micronutrients among older adults are of course only part of the total picture of micronutrient intake, as the proportion of seniors who take vitamin and mineral supplements is steadily on the rise( Reference Fabian, Bogner and Kickinger 48 ). In the Netherlands, during the period between 2010 and 2012, approximately 26 % of women and 18 % of men took vitamin D supplements of at least 10 μg throughout the year. Slightly higher percentages took the same amount of vitamin D daily during the winter months only( Reference Ocke, Buursma-Rethans and de Boer 49 ). A German study in 2009 among older adults showed a high proportion of the population consuming vitamin and mineral supplements regularly – 34 % of men and 54 % of women( Reference Schwab, Heier and Schneider 50 ). Regular consumption of individual nutrients such as vitamin D was much lower, with 7 % of men and 19 % of women taking between 7·4 and 10 μg/d. About 14 % of men and 22 % of women were regular consumers of Mg supplements, but the number that met or exceeded the recommendation remained low, at 16 % of men and 18 % of women. According to the Canadian Community Health Survey (micronutrient intakes from foods included in the present report), 45 % of male and 60 % of female older adults in Canada reported consuming supplements during the period of the dietary data collection( 24 ). Another study in a representative population of older Canadian adults (>51 years) showed a high prevalence of supplement use (40 %)( Reference Shakur, Tarasuk and Corey 51 ). For micronutrients that had observed high risks of inadequacies from dietary intake alone (Mg, Zn, Ca, vitamin A, vitamin C and vitamin D), dietary supplements appeared to close the nutrient gap, with the exception of vitamin D, Mg and Ca, where between 12 and 38 % of the adults remained below the EAR( Reference Shakur, Tarasuk and Corey 51 ). This is consistent with another study among older adults in Austria, where older adults who consumed dietary supplements were compared with older adults who did not consume dietary supplements. Vitamin D deficiency (25(OH)D < 50 nmol/l) still existed in 88 % of the total population, whereas 18 % of the supplemented group had adequate status v. 4 % in the control group( Reference Fabian, Bogner and Kickinger 48 ).

Nutrient recommendations and dietary assessment methods influencing the interpretations of micronutrient intake adequacy

One of the largest problems related to dietary assessment and inter-group comparisons is the lack of harmonisation in nutrient recommendations( Reference Roman Vinas, Ribas Barba and Ngo 23 , Reference Doets, de Wit and Dhonukshe-Rutten 52 ). For example, there are twenty-two different recommendations for vitamin D cited for adults aged 70 years or older in Europe( Reference Ribas-Barba, Serra-Majem and Roman-Vinas 53 ). These range from 2·5 to 15 μg/d, with a median or 7·5 μg/d for men and 10 μg/d for women. The most frequently used value was 10 μg/d (which was the EAR used for both men and women in the present review). Therefore, the percentage of the population at risk for inadequacy is sensitive to the recommendation that is selected. Comparison to a recommendation from another expert committee could therefore influence the present conclusions.

A practical example of the effects of recommendations on calculating the percentage at risk for inadequacy occurred in the present dataset. There was a large sex difference between the percentages at risk for inadequate intakes observed with Mg. Although the Mg intakes were similar (with mean intakes of 296 and 294 mg/d for men and women, respectively), the percentage at risk of inadequate intake was substantially different (73 % for men and 41 % for women) because the EAR are 350 mg/d for men and 265 mg/d for women. Although the Institute of Medicine Mg recommendations contain age- and sex-specific EAR, the scientific evidence supporting these recommendations is limited. Mg balance studies were used, and studies were absent for several age categories and for women in particular. Differences in total energy consumption, and therefore in Mg consumption, between men and women might have influenced the recommendations. Although the most recent age-specific EAR were chosen for the present comparison, the differences between the scientific substantiation of the nutritional recommendations should be considered. In general, there is a need for high-quality markers of nutritional status and for studies performed in (community-dwelling) older adults. Because the recommendations used were published in 1997–2011, more recent insights (e.g. those based on intervention studies on functional outcomes) may affect the present conclusion.

In addition to recommendations, dietary assessment methods also influence the calculation of the population at risk for inadequate intake( Reference Ribas-Barba, Serra-Majem and Roman-Vinas 53 , Reference Tabacchi, Wijnhoven and Branca 54 ). Dietary surveys sometimes rely on memory recalls from older adults, and it is unknown to what extent memory impairments and cognitive functioning influence the reliability of the data( Reference van Staveren and de Groot 3 ). As stated by Ribas-Barba et al. ( Reference Ribas-Barba, Serra-Majem and Roman-Vinas 53 ), there is currently no perfect dietary assessment method for measuring usual intake. Each measurement has its advantages and disadvantages, and each has its own appropriateness regarding the unique needs of the population and the objective. Moreover, the threshold we selected ( ≥ 30 % at risk for inadequacy) to define nutrients of potential concern included a buffer to account for dietary assessment error( Reference de Vries, de Groot and van Staveren 55 ).

Another factor that influences inter-group comparison is the different food composition tables that are used to calculate nutrient intake. The quality and content of food composition tables often differ by country, and this may have introduced variation among the studies included in the present analysis. The time span of the included studies should also be considered, because dietary habits and food compositions change over time.

Strengths and limitations

The present study has a few limitations which should be mentioned. The main limitation is that it represents a small part of a larger clinical picture of intake, absorption, supplement/medication use and functional impairments or outcomes. Although examining all aspects simultaneously in such a large population is not possible, it is difficult to interpret information about the dietary inadequacies of older adults without also considering the other factors. We have attempted to carefully examine each of these dynamic areas and to position our conclusions within this theoretical context. However, it is important to mention that monitoring the status of micronutrients is important in senior populations, even though intake and status are not always well correlated. One example is 25(OH)D status, which is determined not only by nutritional intake but also by sun exposure. Another example is Ca status, for which no accurate marker is currently available.

Many studies did not report whether the intake came from food alone or whether supplement intakes were included in the estimations. In addition, studies that did report supplement intake often only stated the percentage of supplement users and not the types or amounts of supplemented nutrients. This illustrates that there is a need for assessing and better reporting supplement intake in the older adult population. As the proportion of older adults who consume supplements increases( Reference Peklar, Henman and Richardson 56 ), this is becoming an important methodological concern, because it affects our insight into the true extent of micronutrient inadequacies among this population. In the present data analysis, the studies that included supplement intake did not show a consistently low prevalence of nutrient inadequacies. Although information on supplement intake was limited, we do not expect that the studies that included supplement intake strongly influenced our conclusions. Food fortification might also have affected our conclusions, because we did not have insight into the food composition data. This additional source should be considered when interpreting the results for a specific country, as foods are fortified (e.g. vitamin D in dairy, iodine in discretionary salt) in some Western countries. In addition, several countries have supplementation advice (e.g. vitamin D).

Safety levels of the micronutrient intakes were not assessed in the present systematic review. However, they may be of concern for certain nutrients, such as Na. In the present pooled population, Na intake was 3·1 (sd 0·6) g/d in men and 2·5 (sd 0·5) g/d in women, which exceed the recommended upper limits of 2·3 g/d( 20 ).

The choice to include only Western populations was made in order to describe potential inadequacies in the patterns of populations that are most homogeneous. However, this choice could have excluded relevant populations, which may have affected the external validity of our findings. For example, including Japan and Brazil might attenuate or exaggerate apparent nutrients of concern given the wide diversity of traditional dietary patterns. As such, the presented results may provide a proxy for existing dietary inadequacies; however, they may not be representative of global populations of community-dwelling older adults.

We have assumed normality for the present analysis, but the distribution might have been tailed for some nutrients. As a consequence, the inadequacies for these nutrients might have been over- or underestimated.

Nevertheless, there are also strengths to the present review. The main strength is that it gives a robust overview with a large pooled sample size of dietary intakes of vitamins and minerals in Western countries. Thus, this makes the results in the present study more generalisable to Western populations as compared to those in cross-country comparisons. We used a systematic approach to evaluate the quality and risk of bias in each study, which allowed us to perform a robust sensitivity analysis between quality groups. This rigorous method allowed us to present the pooled results with confidence.

Conclusion

In the present systematic review, we identified six nutrients which may be consumed at inadequate amounts at a population level: vitamin D, thiamin, riboflavin, Ca, Mg and Se. Although several other factors are known to influence total micronutrient intakes and, ultimately, nutrient status, the present review provides an important and robust snapshot of the types and magnitude of nutrient intake concerns among Western community-dwelling older adults.

Supplementary material

To view supplementary material for the present article, please visit http://dx.doi.org/10.1017/S0007114515000203

Acknowledgements

We gratefully acknowledge the Dutch National Institute for Public Health and the Environment for providing us with additional raw data from the Ocke et al. ( Reference Ocke, Buursma-Rethans and de Boer 49 ) report. We are grateful to Radoslava Trifonova for her expert help in searching for the articles and to Janneke van Wijngaarden for her thoughtful feedback on the manuscript.

The present work was supported by Nutricia Research, Nutricia Advanced Medical Nutrition.

The author's contributions are as follows: S. t. B. was involved with the data collection and analysis. J. H. assisted with the data collection and analysis and drafted the manuscript. All authors were involved in the study design, data interpretation and manuscript revisions.

S. t. B., J. H., S. V. and Y. C. L. are employees at Nutricia Research. D. M. M., J. M. G. A. S. and L. C. P. G. M. d. G. have no conflicts of interests to declare.

References

1 United Nations Population Fund, HelpAge International (2012) Aging in the twenty-first century. http://www.unfpa.org/public/op/edit/home/publications/pid/11584 (accessed April 2014)..Google Scholar
2 Schilp, J, Kruizenga, HM, Wijnhoven, HA, et al. (2012) High prevalence of undernutrition in Dutch community-dwelling older individuals. Nutrition 28, 11511156.CrossRefGoogle ScholarPubMed
3 van Staveren, WA & de Groot, LC (2011) Evidence-based dietary guidance and the role of dairy products for appropriate nutrition in the elderly. J Am Coll Nutr 30, 429S437S.Google Scholar
4 Houston, DK, Stevens, J, Cai, J, et al. (2005) Dairy, fruit, and vegetable intakes and functional limitations and disability in a biracial cohort: the Atherosclerosis Risk in Communities Study. Am J Clin Nutr 81, 515522.Google Scholar
5 de Groot, CP, van den Broek, T & van Staveren, W (1999) Energy intake and micronutrient intake in elderly Europeans: seeking the minimum requirement in the SENECA study. Age Ageing 28, 469474.Google Scholar
6 Marshall, TA, Stumbo, PJ, Warren, JJ, et al. (2001) Inadequate nutrient intakes are common and are associated with low diet variety in rural, community-dwelling elderly. J Nutr 131, 21922196.CrossRefGoogle ScholarPubMed
7 Zhu, K, Devine, A, Suleska, A, et al. (2010) Adequacy and change in nutrient and food intakes with aging in a seven-year cohort study in elderly women. J Nutr Health Aging 14, 723729.CrossRefGoogle Scholar
8 Semba, RD, Bartali, B, Zhou, J, et al. (2006) Low serum micronutrient concentrations predict frailty among older women living in the community. J Gerontol 61, 594599.Google Scholar
9 Inzitari, M, Doets, E, Bartali, B, et al. (2011) Nutrition in the age-related disablement process. J Nutr Health Aging 15, 599604.CrossRefGoogle ScholarPubMed
10 Moher, D, Liberati, A, Tetzlaff, J, et al. (2009) Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 6, e1000097.CrossRefGoogle ScholarPubMed
11 Bermudez, OI, Falcon, LM & Tucker, KL (2000) Intake and food sources of macronutrients among older Hispanic adults: association with ethnicity, acculturation, and length of residence in the United States. J Am Diet Assoc 100, 665673.Google Scholar
12 Velho, S, Marques-Vidal, P, Baptista, F, et al. (2008) Dietary intake adequacy and cognitive function in free-living active elderly: a cross-sectional and short-term prospective study. Clin Nutr 27, 7786.Google Scholar
13 Wells, GA, Shea, B & O'Connell, D, et al. (2011) The Newcastle–Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. http://www.ohri.ca/programs/clinical_epidemiology/oxford.asp (accessed December 2012)..Google Scholar
14 Cochrane Form III for the evaluation of a cohort-study (Formulier III: voor de beoordeling van het cohortonderzoek) (2012) Coding manual for cohort studies. http://dcc.cochrane.org/sites/dcc.cochrane.org/files/uploads/cohort.pdf (accessed November 2012)..Google Scholar
15 Elmadfa, I, Meyer, A, Nowak, V, et al. (2009) European nutrition and health report 2009. Ann Nutr Metab 55, Suppl. 2, S1S40.Google Scholar
16 EFSA Panel on Dietetic Products Nutrition and Allergies (NDA) (2012) Scientific opinion on the tolerable upper intake level of vitamin D. EFSA J 10, 45.Google Scholar
17 Nordic Council of Ministers (2005) Nordic Nutrition Recommendations 2004, Integrating Nutrition and Physical Activity, 4th ed. Copenhagen: Nordic Council of Ministers.Google Scholar
18 Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food Nutrition Board, Institute of Medicine (1997) Chapter 4 – calcium. In Dietary Reference Intakes for Calcium, Phosphorus, Magnesium, Vitamin D, and Fluoride. Washington, DC: National Academy Press. http://www.nal.usda.gov/fnic/DRI/DRI_Calcium/calcium_full_doc.pdf (accessed accessed April 2014).Google Scholar
19 Ross, AC, Manson, JE, Abrams, SA, et al. (2011) The 2011 dietary reference intakes for calcium and vitamin D: what dietetics practitioners need to know. J Am Diet Assoc 111, 524527.Google Scholar
20 Panel on Dietary Reference Intakes for Electrolytes and Water, Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board et al. (2005) Dietary Reference Intakes for Water, Potassium, Sodium, Chloride, and Sulfate. Washington, DC: Institute of Medicine.Google Scholar
21 National Research Council (2000) Dietary Reference Intakes: Applications in Dietary Assessment. Washington, DC: The National Academies Press.Google Scholar
22 Mensink, GB, Fletcher, R, Gurinovic, M, et al. (2013) Mapping low intake of micronutrients across Europe. Br J Nutr 110, 755773.Google Scholar
23 Roman Vinas, B, Ribas Barba, L, Ngo, J, et al. (2011) Projected prevalence of inadequate nutrient intakes in Europe. Ann Nutr Metab 59, 8495.CrossRefGoogle ScholarPubMed
24 Health Canada, Statistics Canada (2009) Canadian Community Health Survey, Cycle 2.2, Nutrition, (2004). Nutrient Intakes from Food, Provincial, Regional and National Summary Data Tables, Volume 1, 2 and 3. Ottawa: Health Canada.Google Scholar
25 van Rossum, CTM, Fransen, HP, Verkaik-Kloosterman, J, et al. (2011) Dutch National Food Consumption Survey 2007–2010, Diet of Children and Adults Aged 7 to 69 Years. Report no. 350050006/2011 . Bilthoven: National Institute for Public Health and the Environment.Google Scholar
26 Brouwer-Brolsma, EM (2013) Vitamin D: do we get enough? A discussion between vitamin D experts in order to make a step towards the harmonisation of dietary reference intakes for vitamin D across Europe. Osteoporos Int 24, 15671577.Google Scholar
27 Brock, KE, Ke, L, Tseng, M, et al. (2013) Vitamin D status is associated with sun exposure, vitamin D and calcium intake, acculturation and attitudes in immigrant East Asian women living in Sydney. J Steroid Biochem Mol Biol 136, 214217.Google Scholar
28 Mithal, A, Wahl, DA, Bonjour, JP, et al. (2009) Global vitamin D status and determinants of hypovitaminosis D. Osteoporos Int 20, 18071820.Google Scholar
29 Ginter, JK, Krithika, S, Gozdzik, A, et al. (2013) Vitamin D status of older adults of diverse ancestry living in the Greater Toronto Area. BMC Geriatr 13, 66.Google Scholar
30 Chung, M, Balk, EM, Brendel, M, et al. (2009) Vitamin D and calcium: a systematic review of health outcomes. Evid Rep Technol Assess (Full Rep) 1420.Google Scholar
31 Witkowski, M, Hubert, J & Mazur, A (2011) Methods of assessment of magnesium status in humans: a systematic review. Magnes Res 24, 163180.Google Scholar
32 Heaney, RP (2008) Vitamin D and calcium interactions: functional outcomes. Am J Clin Nutr 88, 541S544S.Google Scholar
33 Scott, D, Blizzard, L, Fell, J, et al. (2010) Associations between dietary nutrient intake and muscle mass and strength in community-dwelling older adults: the Tasmanian Older Adult Cohort Study. J Am Geriatr Soc 58, 21292134.Google Scholar
34 Dominguez, LJ, Barbagallo, M, Lauretani, F, et al. (2006) Magnesium and muscle performance in older persons: the InCHIANTI study. Am J Clin Nutr 84, 419426.Google Scholar
35 Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board, Institute of Medicine (1998) Dietary Reference Intakes for Thiamin, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic acid, Biotin, and Choline. Washington, DC: The National Academies Press. http://www.nal.usda.gov/fnic/DRI//DRI_Thiamin/full_report.pdf (accessed accessed April 2014).Google Scholar
36 Center for Disease Control (2012) Second national report on biochemical indicators of diet and nutrition in the U.S. population. http://www.cdc.gov/nutritionreport/pdf/Nutrition_Book_complete508_final.pdf#zoom = 100 (accessed April 2014)..Google Scholar
37 Allen, LH (2009) How common is vitamin B-12 deficiency? Am J Clin Nutr 89, 693S696S.Google Scholar
38 Bor, MV, Lydeking-Olsen, E, Moller, J, et al. (2006) A daily intake of approximately 6 microg vitamin B-12 appears to saturate all the vitamin B-12-related variables in Danish postmenopausal women. Am J Clin Nutr 83, 5258.Google Scholar
39 van Wijngaarden, JP, Doets, EL, Szczecinska, A, et al. (2013) Vitamin B12, folate, homocysteine, and bone health in adults and elderly people: a systematic review with meta-analyses. J Nutr Metab 2013, 486186.Google Scholar
40 Doets, EL, van Wijngaarden, JP, Szczecinska, A, et al. (2013) Vitamin B12 intake and status and cognitive function in elderly people. Epidemiol Rev 35, 221.Google Scholar
41 Jacobsen, DW (1998) Homocysteine and vitamins in cardiovascular disease. Clin Chem 44, 18331843.Google Scholar
42 Refsum, H, Nurk, E, Smith, AD, et al. (2006) The Hordaland Homocysteine Study: a community-based study of homocysteine, its determinants, and associations with disease. J Nutr 136, 1731S1740S.Google Scholar
43 van Schoor, NM, Swart, KM, Pluijm, SM, et al. (2012) Cross-sectional and longitudinal association between homocysteine, vitamin B12 and physical performance in older persons. Eur J Clin Nutr 66, 174181.Google Scholar
44 Homocysteine Lowering Trialists' Collaboration (1998) Lowering blood homocysteine with folic acid based supplements: meta-analysis of randomised trials. BMJ 316, 894898.Google Scholar
45 Semba, RD, Ricks, MO, Ferrucci, L, et al. (2009) Low serum selenium is associated with anemia among older adults in the United States. Eur J Clin Nutr 63, 9399.Google Scholar
46 Thomson, CD (2004) Assessment of requirements for selenium and adequacy of selenium status: a review. Eur J Clin Nutr 58, 391402.Google Scholar
47 van Kappel, AL, Steghens, JP, Zeleniuch-Jacquotte, A, et al. (2001) Serum carotenoids as biomarkers of fruit and vegetable consumption in the New York Women's Health Study. Public Health Nutr 4, 829835.Google Scholar
48 Fabian, E, Bogner, M, Kickinger, A, et al. (2012) Vitamin status in elderly people in relation to the use of nutritional supplements. J Nutr Health Aging 16, 206212.Google Scholar
49 Ocke, MC, Buursma-Rethans, EJM, de Boer, EJ, et al. (2013) Diet of Community-dwelling Older Adults: Dutch National Food Consumption Survey Older Adults 2010–2012. Bilthoven: National Institute for Public Health, Sport and the Environment.Google Scholar
50 Schwab, S, Heier, M, Schneider, A, et al. (2014) The use of dietary supplements among older persons in Southern Germany – results from the KORA-age study. J Nutr Health Aging 18, 510519.Google Scholar
51 Shakur, YA, Tarasuk, V, Corey, P, et al. (2012) A comparison of micronutrient inadequacy and risk of high micronutrient intakes among vitamin and mineral supplement users and nonusers in Canada. J Nutr 142, 534540.Google Scholar
52 Doets, EL, de Wit, LS, Dhonukshe-Rutten, RA, et al. (2008) Current micronutrient recommendations in Europe: towards understanding their differences and similarities. Eur J Nutr 47, Suppl. 1, 1740.Google Scholar
53 Ribas-Barba, L, Serra-Majem, L, Roman-Vinas, B, et al. (2009) Effects of dietary assessment methods on assessing risk of nutrient intake adequacy at the population level: from theory to practice. Br J Nutr 101, Suppl. 2, S64S72.Google Scholar
54 Tabacchi, G, Wijnhoven, TM, Branca, F, et al. (2009) How is the adequacy of micronutrient intake assessed across Europe? A systematic literature review. Br J Nutr 101, Suppl. 2, S29S36.Google Scholar
55 de Vries, JH, de Groot, LC & van Staveren, WA (2009) Dietary assessment in elderly people: experiences gained from studies in the Netherlands. Eur J Clin Nutr 63, Suppl. 1, S69S74.Google Scholar
56 Peklar, J, Henman, MC, Richardson, K, et al. (2013) Food supplement use in the community dwelling population aged 50 and over in the Republic of Ireland. Complement Ther Med 21, 333341.Google Scholar
57 EURopean micronutrient RECommendations Aligned (EURRECA) (2009) Defining data for assessment of intake and status adequacy from open access and grey literature. http://www.eurreca.org/everyone/8567/7/0/32 (accessed April 2014).Google Scholar
58 Adamson, AJ, Collerton, J, Davies, K, et al. (2009) Nutrition in advanced age: dietary assessment in the Newcastle 85+ study. Eur J Clin Nutr 63, Suppl. 1, S6S18.Google Scholar
59 Bates, E, Lennox, A & Bates, C, et al. (2011) National diet and nutrition survey. Headline results from years 1 and 2 (combined) of the rolling programme (2008/2009–2009/2010). http://www.gov.uk/government/uploads/system/uploads/attachment_data/file/216484/dh_128550.pdf (accessed April 2014)..Google Scholar
60 Becker, W & Pearson, M (2002) Riksmaten 1997–98. Dietary Habits and Nutrient Intake in Sweden. Uppsala: Livsmedelsverket, National Food Agency.Google Scholar
61 Boilson, A, Staines, A, Kelleher, CC, et al. (2012) Unmetabolized folic acid prevalence is widespread in the older Irish population despite the lack of a mandatory fortification program. Am J Clin Nutr 96, 613621.Google Scholar
62 Castetbon, K, Vernay, M, Malon, A, et al. (2009) Dietary intake, physical activity and nutritional status in adults: the French nutrition and health survey (ENNS, 2006–2007). Br J Nutr 102, 733743.Google Scholar
63 Decarli, B, Dirren, H & Schlettwein-Gsell, D (1998) Swiss survey in Europe on nutrition and the elderly: nutritional status of a Yverdon population aged 74 to 79 years old over a period of four years. Rev Med Suisse Romande 118, 701707.Google Scholar
64 Elmadfa, I, Freisling, H, Nowak, V, et al. (2009) Österreichischer ernährungsbericht 2008 (Austrian Nutrition Report 2008). Wien: Bundesministerium für Gesundheit.Google Scholar
65 Feart, C, Alles, B, Merle, B, et al. (2012) Adherence to a Mediterranean diet and energy, macro-, and micronutrient intakes in older persons. J Physiol Biochem 68, 691700.CrossRefGoogle ScholarPubMed
66 Fidanza, F, Simonetti, MS, Mariani Cucchia, L, et al. (1984) Nutritional status of the elderly. II. Anthropometry, dietary and biochemical data of old pensioners in Perugia at the fifth year follow-up. Int J Vitam Nutr Res 54, 7590.Google Scholar
67 Finch, S, Doyle, W, Lowe, S, et al. (1998) National Diet and Nutrition Survey: People Aged 65 Years and Over. Volume 1: Report of the Diet and Nutrition Survey. London: The Stationery Office.Google Scholar
68 Gibson, S (2001) Dietary sugars and micronutrient dilution in normal adults aged 65 years and over. Public Health Nutr 4, 12351244.Google Scholar
69 Griep, MI, Verleye, G, Franck, AH, et al. (1996) Variation in nutrient intake with dental status, age and odour perception. Eur J Clin Nutr 50, 816825.Google Scholar
70 Horwath, CC, Campbell, AJ & Busby, W (1992) Dietary survey of an elderly New Zealand population. Nutr Res 12, 441453.Google Scholar
71 Hulshof, KFAM & van Staveren, WA (1991) The Dutch national food consumption survey: design, methods and first results. Food Policy 16, 257260.Google Scholar
72 Johansson, L & Solvoll, K (1999) Norkost 1997. Landsomfattende kostholdsundersøkelse blant menn og kvinner i alderen 16-79 år (Norkost 1997. National Food Consumption Survey among Men and Women Aged 16–79 Years). Oslo: Statens råd for ernæring og fysisk aktivitet.Google Scholar
73 Konstantinova, SV, Tell, GS, Vollset, SE, et al. (2008) Dietary patterns, food groups, and nutrients as predictors of plasma choline and betaine in middle-aged and elderly men and women. Am J Clin Nutr 88, 16631669.Google Scholar
74 Lopes, C, Oliveira, A, Santos, AC, et al. (2006) Consumo alimentar no Porto (Food Consumption in Porto). Porto: Department of Hygiene and Epidemiology.Google Scholar
75 Luhrmann, PM, Herbert, BM & Neuhauser-Berthold, M (2001) Underreporting of energy intake in an elderly German population. Nutrition 17, 912916.Google Scholar
76 Max Rubner-Institut (2008) Nationale verzehrsstudie II. Ergebnisbericht teil 1. Die bundesweite befragung zur ernahrung von jugendlichen und erwachsenen (National Consumption Study II. Results Report Part 1. The National Survey on Nutrition of Adolescents and Adults). Karlsruhe: Max Rubner-Institut.Google Scholar
77 Milman, N, Pedersen, AN, Ovesen, L, et al. (2004) Iron status in 358 apparently healthy 80-year-old Danish men and women: relation to food composition and dietary and supplemental iron intake. Ann Hematol 83, 423429.Google Scholar
78 Mowe, M, Bohmer, T & Kindt, E (1994) Reduced nutritional status in an elderly population (>70 y) is probable before disease and possibly contributes to the development of disease. Am J Clin Nutr 59, 317324.Google Scholar
79 Nelson, C, Wengreen, HJ, Munger, RG, et al. (2009) Dietary folate, vitamin B-12, vitamin B-6 and incident Alzheimer's disease: the Cahce county memory, health, and aging study. J Nutr Health Aging 13, 899905.Google Scholar
80 Nicolas, AS, Faisant, C, Nourhashemi, F, et al. (2001) Nutrient adequacy of dietary intake in a healthy elderly French population. Eur J Ger 3, 140145.Google Scholar
81 Ortega, RM, Requejo, AM, Andres, P, et al. (1997) Dietary intake and cognitive function in a group of elderly people. Am J Clin Nutr 66, 803809.Google Scholar
82 Pedersen, AN, Fagt, S, Groth, M, et al. (2010) Dietary Habits in Denmark 2003–2008. Main Results. Søborg: DTU Food, National Food Institute.Google Scholar
83 Pietinen, P, Paturi, M, Reinivuo, H, et al. (2010) FINDIET 2007 survey: energy and nutrient intakes. Public Health Nutr 13, 920924.Google Scholar
84 Posner, BM, Jette, A, Smigelski, C, et al. (1994) Nutritional risk in New England elders. J Gerontol 49, M123M132.Google Scholar
85 Rothenberg, E, Bosaeus, I & Steen, B (1996) Food habits and nutrient intake in three 70-year-old free-living populations in Gothenburg, Sweden. A 22-year cohort study. Scand J Nutr 40, 104110.Google Scholar
86 Serra Majem, L, Ribas Barba, L, Salvador Castell, G, et al. (2006) Avaluació de l'estat nutricional de la població catalana 2002–2003. Evolució dels hàbits alimentaris i dels consum d'aliments i nutrients a Catalunya (1992–2003) (Assessment of Nutritional Status of the Catalan Population 2002–2003. Evolution of Food Habits and Consumption of Food and Nutrients in Catalonia (1992–2003)). Barcelona: Departament de salut, Generalitat de Catalunya.Google Scholar
87 Sette, S, Le Donne, C, Piccinelli, R, et al. (2011) The third Italian national food consumption survey, INRAN-SCAI 2005-06-part 1: nutrient intakes in Italy. Nutr Metab Cardiovasc Dis 21, 922932.Google Scholar
88 Szponar, L, Sekula, W, Nelson, M, et al. (2001) The household food consumption and anthropometric survey in Poland. Public Health Nutr 4, 11831186.Google Scholar
89 Toffanello, ED, Inelmen, EM, Minicuci, N, et al. (2011) Ten-year trends in vitamin intake in free-living healthy elderly people: the risk of subclinical malnutrition. J Nutr Health Aging 15, 99103.CrossRefGoogle ScholarPubMed
90 U.S. Department of Agriculture, Agricultural Research Service (2012) Nutrient intakes from food: mean amounts consumed per individual, by gender and age, what we eat in America, NHANES 2009–2010. http://www.ars.usda.gov/ba/bhnrc/fsrg (accessed April 2014)..Google Scholar
91 Zoltick, ES, Sahni, S, McLean, RR, et al. (2011) Dietary protein intake and subsequent falls in older men and women: the Framingham Study. J Nutr Health Aging 15, 147152.Google Scholar
Figure 0

Table 1 Overview of the study quality assessment*

Figure 1

Table 2 Characteristics of the included studies, assessing nutrient intake in community-dwelling older adults

Figure 2

Fig. 1 Systematic reviews and meta-analyses (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) flowchart of article selection and inclusion.

Figure 3

Table 3 Daily vitamin intake and percentage of inadequate intakes among older adults (Mean values and standard deviations; percentages and 95 % confidence intervals)

Figure 4

Fig. 2 Mean (95 % CI) percentage of men () and women () at risk for inadequate intake of vitamins.

Figure 5

Table 4 Daily mineral intake and percentage of inadequate intakes among older adults (Mean values and standard deviations; percentages and 95 % confidence intervals)

Figure 6

Fig. 3 Mean (95 % CI) percentage of men () and women () at risk for inadequate intake of minerals.

Supplementary material: PDF

ter Borg supplementary material

Tables S1-S5

Download ter Borg supplementary material(PDF)
PDF 730.2 KB