Anthropometric
Anthropometric
net/publication/14752015
Effect of flavor enhancement of foods for the elderly on nutritional status: Food
intake, biochemical indices, and anthropometric measures
CITATIONS READS
209 1,598
2 authors, including:
Susan Schiffman
North Carolina State University
276 PUBLICATIONS 11,687 CITATIONS
SEE PROFILE
Some of the authors of this publication are also working on these related projects:
All content following this page was uploaded by Susan Schiffman on 01 November 2017.
S U S A N S. S C H I F F M A N l A N D Z O E S. W A R W I C K
Departments of Psychiatry and Psychology, Duke University, Durham, N C 27706, and The Sarah W. Stedman
Center for Nutritional Studies, Duke University Medical Center, Durham, N C 27710
R e c e i v e d 8 S e p t e m b e r 1992
SCHIFFMAN, S. S. AND Z. S. WARWICK. Effect offlavor enhancement offoods for the elderly on nutritional status: Food
intake, biochemical indices, and anthropometric measures. PHYSIOL BEHAV 53(2) 395-402, 1993.--The irreversible declines
in taste and smell acuity that occur in many elderly persons can contribute to inadequate food intake and nutrition that are
prevalent among the aged. Although chemosensory deficits cannot be reversed, previous studies have shown that the addition of
intense flavors to foods can compensate for perceptual losses and improve food palatability and acceptance. In this study, the
effect of sustained (3 week) flavor enhancement of typical institutional foods on the diet, health, and well being of 39 elderly
(average age 84.6 SE 0.81 years) retirement-home residents was evaluated. For 3 weeks subjects ate an institutionaldiet (unenhanced).
During another 3-week period, the same subjects ate identical foods to which intense flavors were added (enhanced). The 39
subjects were tested in two groups. For group I the unenhanced food period preceded the enhanced food period. For group 2,
the order was reversed. Food intake was measured every weekday throughout the study, and the nutritional composition of the
diet was analyzed. Biochemical measures of health status were obtained at the beginning of the study (baseline) and following
both the unenhanced and enhanced periods. These measures included somatomedin-C/insulin-likegrowth factor I, transferrin,
total T- and B-lymphocytes, and routine blood chemistries. Weight, height, midarm circumference, and triceps skinfold thickness
were also measured. Handgrip strength and pinch strength were measured in group I. Three major findings emerged from this
study: 1) elderly persons ate more food when it was flavor enhanced, 2) consumption of flavor-enhanced food was associated
with improved immune function that was not attributable to altered nutrient intake or biochemical status, and 3) improved grip
strength in both hands was evident after 3 weeks' consumption of flavor-enhanced foods.
Requests for reprints should be addressed to S. S. Schiffman, Department of Psychology, Duke University, Durham, NC 27706.
395
396 SCHIFFMAN ANI) ~ R W I ( ' I , ,
METHOD
r~ tt-, Lr,
Std!jects
Thirty-nine elderly persons (average age 84.6 SE 0.81 years)
participated in this study. All subjects were independent living
residents at the Methodist Retirement Home, Durham, NC, and
all had permission to participate in the study from their family t¢-., tt-~ o I
physician. All subjects had demonstrated deficits in taste and
smell in previous experiments performed at the Methodist Re- +1 +i 4-1 +I
TABLE 2
FLAVOR-ENHANCED FOODS
a double fold of skin and subcutaneous tissue, the subcutaneous (B-l), riboflavin (B-2), niacin (B-3), pyridoxine (B-6), cobalamin
fat was separated from the underlying muscle. (B-12), vitamin C, vitamin E, folacin, calcium, iron, magnesium,
The measures of functional status were handgrip strength phosphorus, selenium, and zinc. RDAs have not been established
and pinch strength. Handgrip strength was determined using a for pantothenic acid, copper, potassium, and sodium; instead,
Jamar hand dynamometer (Asimow Engineering Co.-Thera- an intake range for each of these nutrients has been designated
peutic Equipment, Clifton, N J). Measurements of grip strength as the estimated safe and adequate daily dietary intakes (SADDI)
were obtained for both hands at grip positions I through V. Pinch (25). A value within the range was chosen as the reference for
strength was determined using a pinch gauge (Therapeutic computing daily intake as a percentage of the recommended
Equipment, Clifton, N J). Pinch strength was measured in both intake. These reference values were: pantothenic acid, 7 mg;
hands in each of three positions: lateral pinch, two-point pinch, copper, 2.5 mg; potassium, 2000 mg; sodium 2400 mg.
three-point pinch.
Data Analysis
Food Intake
Each subject served as his/her own control, because all sub-
Measurements of food consumption were determined for ev- jects consumed flavor-enhanced foods for 3 weeks, and unen-
ery meal for 5 days of the week. Subjects were served a set tray hanced foods during another 3 weeks. Analysis of variance was
in a dining hall, with all subjects receiving identical trays. Study used to evaluate the significance of differences between data from
participants were seated together and ate in groups of two to the enhanced and the unenhanced conditions. Criterion for sta-
four. All food portions were weighed to the nearest 0.1 g prior tistical significance was p < 0.05.
to serving. Immediately after the meal, the food remaining on Data on grip and pinch strength were combined for left- and
the plate was weighed to the nearest 0.1 g, and the amount eaten righthand dominant subjects, because classifying subjects ac-
determined by subtraction. Nine of the ten persons who mea- cording to hand dominance results in only minor differences
sured plate wastage had no knowledge of the foods that were (20).
amplified. One person had knowledge of the foods to be amplified
on some occasions.
The nutritional composition of each subject's daily food in- RESULTS
take was determined using Food Processor II software (ESHA Biochemical and Anthropometric Measures
Research, Salem, OR). To facilitate interpretation, daily nutrient
consumption was computed as a percentage of ideal intake. The Eating flavor-enhanced foods was associated with an im-
reference values used for computation of this percentage were provement in immune status. This was indicated by B-cell and
as follows: T-cell counts that were higher following 3 weeks of consuming
Calories. These are based on the resting energy expenditure flavor-enhanced foods than levels following 3 weeks of consum-
from the Harris-Benedict equation, plus incremental percentages ing the same foods without flavor enhancement (Table 3). When
of the basal metabolism to allow for muscular activity (6). All the data from both groups were combined, the effect of flavor
subjects in this study were classified as sedentary. enhancement on total lymphocytes, B-cells and T-cells was highly
Protein. Grams (0.8) per kg of body weight. significant, smallest, F(1, 37) = 8.11, p < 0.01. When the data
Carbohydrate. Fifty-eight percent of total calories. for each group were examined separately, the effect of flavor
Total fat. Thirty percent of total calories, with saturated, enhancement was significant only in group 2, all p < 0.025.
monounsaturated and polyunsaturated fats each contributing Data from group 1 showed a trend towards increased immunity
10% of total calories. as a result of flavor enhancement. The increased immunity as-
Micronutrients. Intake of the following nutrients are reported sociated with consumption of flavor-enhanced foods did not
as a percentage of the recommended daily allowance (25) for elevate B-cell and T-cell counts above the normal range. All
older adults, that is, persons 51 years or more: vitamin A, thiamin other biochemical measures were within normal limits and
398 S C H I F F M A N AN[) \ ~ A R W I ( ' K
e~ TABLE 4
~ - _ HANDGRIP AND PINCH STRENGTH
Group I
z,,, 80T
o v 70
I~-Z
=~- 60
~uJ
~ z
Z'q
50
/
Ow
o~
_zm
40
,,,o
O01--
30
II
~_~ 2o
gBz
--l.d
~n,,
10
-10 t
-20
-30
ADDED FLAVOR
FIG. 1. Effect of each type of flavor enhancer, averaged across foods, on intake. Height of bars depicts
increased intake as a result of flavor enhancement.
was almost identical in the enhanced and unenhanced conditions total lymphocyte count was higher in elderly persons who had
(Table 5). It is noteworthy that when data from both groups strong interpersonal relationships (42).
were combined, slight decreases in fat and sodium intake were
found in the enhanced condition. Nutritional Indices
Although the dietary intake was virtually identical in the two
DISCUSSION conditions, intake of some micronutrients was less that the RDA
Major Findings (Table 5). The specific nutrient deficiencies were generally con-
sistent with previous studies of the diet composition of elderly
Three major findings emerged from this study: persons.
1. elderly persons ate more food when it was flavor enhanced; Nutrients Below the RDA in This Study
2. consumption of flavor-enhanced food was associated with
improved immune function that was not attributable to al- Calcium. The mean calcium intake in this study of 35 women
tered nutrient intake or biochemical status, and and 4 men was marginal and averaged 82.7% (enhanced) and
3. improved grip strength in both hands was evident after 3 84.4% (unenhanced) of the RDA. This is consistent with previous
weeks' consumption of flavor-enhanced foods. reports (10,24) of low calcium intake by elderly persons, although
other investigators found that average calcium intake exceeded
These data are consistent with the conclusion that nutritional the RDA for both men and women (27). Low intake of calcium,
status is not the only contributor to immune system function coupled with poor absorption efficiency, both contribute to neg-
in elderly persons. One study (13) found no correlation between ative calcium balance in elderly persons (14). In addition, bio-
the immunologic function and nutritional status of over 200 availability of dietary calcium is influenced by dietary factors
elderly men and women. In the present study, eating flavor- such as phytate and protein levels. Increased consumption of
enhanced foods produced a rise in B-cell and T-cell count, but wheat bran (which contains phytate), and of dietary protein,
did not alter nutritional status as indicated by dietary intake and caused greater fecal loss of calcium in young subjects (29).
biochemical measures. This improved immune status may be Copper. Copper intake in this study was low, averaging 47.5%
due to endogenous opiate (endorphin) effects from stimulation (unenhanced) and 48.7% (enhanced) of the SADDI (estimated
of the limbic system by flavors. safe and adequate dally dietary intake). However, because pre-
Endorphins are multifunctional peptides that regulate both vious research has found that deficiency symptoms are not ev-
affective and physiological well being; for example, endorphin ident despite a putatively low copper intake, it is possible that
activity is linked to both food ingestion (26) and immune system
function (38). Short-term studies (5,7) of young adults indicate 1. food copper levels are actually greater than reported and/or
that pleasure responses to food tastes and flavors are mediated 2. bodily adaptation to low copper intake mitigates the effects
by endogenous opioid activity. The finding in this study of im- of inadequate intake (25).
proved immune status associated with food flavor enhancement Because methods for accurately measuring body copper status
suggests that opioid activity arising from consumption of pal- have not yet been developed, relatively little is known about
atable foods also promotes physiological benefits such as in- copper bioavailability and deficiency in humans (21).
creased immunity. Further evidence for psychological modu- Magnesium. Magnesium intake was low, and averaged only
lation of immune system activity comes from the finding that 79.1% (enhanced) and 81.4% (unenhanced) of the RDA. Low
400 S C H I F F M A N .AND % ' A R W I ( ' K
TABLE 5
NUTRIENT [NTAKE RELATIVE TO RECOMMENDED CONSUMPTION LEVEI.S
Calories 124.(1+ 4.17 120.7_~ 3.81 117.6± 3.28 116.4_+ 3.23 120.4 + 2.61 118.3 ~ 2.46
Protein 139.7_+ 5.91 137.5 ± 6.15 128.9± 6.56 134.8_+ 6.71" 133.6 ± 4.54 136.0±4.58
Carbohydrates 106.0 _+ 3.81 105.2 ± 3.52 99.7 ± 2.66 102.0 _+ 2.73 102.4 _+_. 2.26 103.4 t 2.16
Dietary fiber 63.4 ± 2.72 58.7 + 2.63* 54.1 ± 2.01 55.8 ± 1.78 58.2 ± 1.78 57,1 ~: 1.52
Fat-total 151.2± 4.84 147.0± 4.57 147.3± 4.64 138.3_+ 4.13" 149.0 + 3.33 142.4 ± 3.09*
Fat-saturated 144.7_+ 4.47 147.6+ 4.72 140.1 ± 4.68 140.1 + 4.62 I42,1 ± 3.26 143.3± 3.33
Fat-monounsaturated 177.7 _+ 5.83 171.4 _+ 5.45 171.5 ± 5.27 160.6 ± 4.83* 174,2 ± 3.89 165.3 +- 3.67*
Fat-polyunsaturated 96.0± 3.56 87.1 ± 3.20* 96.8 + 3.48 84.(1+ 2.21" 96,5 + 2.47 85. t e 1.86"
Cholesterol 137.6 ± 8.75 147.9 + 9.28 155.4 ± 10.57 154.5 _+ 9.14 147.6+ 7.14 151.626.49
VitaminA-tolal 179.6± 9.12 163.5 + 8.09* 181.0± 10.42 173.6± 7.27 180.4+ 7.01 169.2 ± 5.40*
Thiamin-Bl 132.7± 6.3 126.1 ± 5.32* 137.1 ± 5.98 130.6+ 4.69* 135.2 ± 4.31 128.7 a 3.49*
Riboflavin-B2 125.9± 6.14 125.7± 6.48 133.1 _+ 7.72 132.6+ 6.78 129.9± 5.08 129.6 24.-'3
Niacin-B3 120.1± 5.16 117.7-+ 4.63 117.9± 4.66 122.1 -~ 3.79 118.9± 3.42 120.1 ~2.92
Pyridoxine-B6 107.8_+, 4.11 108.5+ 3.57 98.3 +_ 3.33 109.2+ 3.07* 1112.4 # 2.67 108.9 ± 2.30
Cobalamin-Bl2 236.8 ± 9.91 188.4+ 11.96" 223.0± 12.52 189.1 + 11.03" 229,0 ± 8.26 188.8 z 8.01
Folacin 139.3± 7.92 119.2+ 6.31" 121.(1_+ 5.82 122,3+ 4.4(I 129.11+ 4.92 121.0-~ 3.66
Pantothenic acid 64.4 ± 3.16 62.4 + 3.21 62.3 ~ 3.32 66.3 + 3.117" 63.2 + 2.30 64.6 :t: 2.22
Vitamin C 276.4 _+ 19.06 215.3 + 13.05" 179.6 + 8.63 197.8 e- 7.13" 221.8 ± 12.27 205.4 t. 7.ot)
Vitamin E 233.4_+ 7.91 252.4 + 11.34 200.5 ± 8.57 255.5 + 7.88 214.8 ± 6.43 2"~4.2 4 6.56
Calcium 82.5 ± 5.61 79.0 ± 6.31 85.9 ± 6.97 85.6 + 6.49 84.4 ± 4.58 82,7 ±4.55
Copper 51.1 ± 2.42 47.8 ± 2.26* 44.7 ± 1.76 49.4+ 1.76 47.5 + 1.52 48.7 ± 1.39
Iron 121.3± 5.12 117.2± 5.49 120.1± 4.73 121.8± 4.40 120.6 ± 3.44 119.8 ± 3.42
Magnesium 86.8± 3.62 79.1 ± 3.33* 77.2± 3.31/ 79.1 ± 2.90 81.4 + 2.53 79.1 ± 2.16
Phosphorus 131.2 _+: 6.22 133.4 ± 6.85 138.4 ± 7.43 140.9 + 6.91 135.3 ± 4.96 137.6 ±4.89
Potassium 69.7± 3.33 66.0+ 3.16" 64.7± 2.90 68.1 + 2.72* 66.9 + 2.20 67.2 ± 2.1,14
Selenium 81.0± 6.19 79.3 + 6.21 87.9± 8.07 91.4± 7.44* 84.9 *_ 5.26 86. L ± 5.03
Sodium 108.4± 5.12 1114.6 ± 4.63 116.4± 492 108.2:~ 4.21" 112.q+ 3.57 106.6 ~ 3.09*
Zinc 73.8 ± 3.07 75.2 ± 3.37 73.5 ± 3.13 77.0 + 3.15" 7~,.6 ± 2.19 76.2 :+ 2.28*
Values are mean _+ SE of percent of dietary guidelines [br optimal intake (see text for reference values used in calculation).
* Significantly different from group value in unenhanced condition.
magnesium intake by both free-living and institutionalized el- Nutrients at or Above the RDA in Ibis Study
derly has been reported (44). Cobalamin (B-12). Intake of c o b a l a m i n exceeded the RDA,
Pantothenic acid. Intake of p a n t o t h e n i c acid was low, aver- a n d averaged 188.8% (enhanced) to 229.0% ( u n e n h a n c e d ) o f the
aging 63.2% (unenhanced) and 64.6% (enhanced) of the SADDI. RDA. This finding is consistent with previous reports (10,27)
This finding of inadequate p a n t o t h e n i c acid intake is consistent of adequate c o b a l a m i n intake by the elderly.
with previous evaluations of the p a n t o t h e n i c acid content of Folacin. Intake of folacin was adequate, a n d averaged 121.0%
nursing h o m e diets (24,45). However, Srinivasan et al. (39) found (enhanced) and 129.0% ( u n e n h a n c e d ) of the RDA. It should be
that 91% of elderly people studied c o n s u m e d at least 4 m g of noted that the 1989 RDAs for folate (men, 200 ug; women, 180
p a n t o t h e n i c acid daily, which is within the range of the SADD1. ~g) are m u c h lower t h a n the 1980 RDAs (men a n d women, 400
Potassium. Potassium intake was low, averaging approxi- ug). For this reason, previous reports (10,27) of inadequate intake
mately 67% of the SADDI in both the enhanced and u n e n h a n c e d of folate by the elderly would, according to the 1989 RDAs,
conditions. This finding is consistent with other reports of low indicate that folate intake was adequate.
potassium intake a m o n g certain groups of elderly persons (44). Iron. Iron intake was adequate, averaging 119.8% (enhanced)
Selenium. Selenium intake was below the RDA, and averaged a n d 120.6% ( u n e n h a n c e d ) o f the RDA. This is consistent with
84.9% ( u n e n h a n c e d ) a n d 86.1% (enhanced). Megadoses of se- previous reports of generally adequate iron intake a m o n g the
lenium a n d vitamin E have been reported to improve certain elderly (10,19,27), although one study (24) found average dietary
mental characteristics of geriatric nursing h o m e residents in iron intake to be below the RDA.
Finland (43). Although some findings suggest that high levels of Niacin (B-3). Niacin intake exceeded the RDA, averaging
dietary selenium reduce the incidence of tumors, other studies 118.9% ( u n e n h a n c e d ) a n d 120.1% (enhanced) of the RDA. Pre-
have not found a protective effect o f selenium on cancer Ire- vious studies (10,24,27) have also found adequate dietary intake
viewed in (211]. of niacin by elderly persons.
Zinc. Zinc intake was marginal, a n d averaged 73.6% (un- Phosphorus. Intake of p h o s p h o r u s was adequate, a n d aver-
enhanced) a n d 76.2% (enhanced) of the RDA. T h e diet of m a n y aged 135.3% ( u n e n h a n c e d ) a n d 137.6% (enhanced). This is con-
elderly persons tends to be low in zinc (2,24,41), although a n sistent with a previous report of adequate phosphorus intake by
age-related increase in serum zinc in m e n has been reported elderly persons (10).
(15). Phytate, a constituent of wheat flour, impairs absorption Protein. T h e m e a n protein intake in this study ranged from
of zinc (29). 133.6 to 136% of the RDA. This is consistent with the findings
FLAVOR ENHANCEMENT OF FOOD FOR ELDERLY 401
of Munro et al. (23) who determined that dietary protein is gen- 1. The recommended daily allowances of certain nutrients may
erally adequate in elderly persons. For example, elderly Chinese be far higher than is necessary to ensure adequate nutrition
were found to have a daily protein intake of 1.2 g/kg (47), which of most persons.
is 50% higher than the recommended 0.8 g/kg. 2. Another important consideration is that the reported values
Pyridoxine (B-6). Pyridoxine intake was slightly higher than for the nutritional composition of some foods may be inac-
the RDA, averaging 102.4% (unenhanced) and 108.9% (en- curate.
hanced). This is somewhat atypical, because pyridoxine intake
by elderly persons has often been reported as below the RDA The subjects in the present study had an average daily calorie
(10,40,27). intake above the recommended level during both diet periods
Riboflavin (B-2). Riboflavin intake was adequate, and aver- (Table 5), yet no changes in body weight occurred during the 6
aged 129.6% (enhanced) and 129.9% (unenhanced) of the RDA. weeks (Table 1). At least two explanations are possible.
This finding is consistent with previous studies that found ad- 1. The recommended calorie intake for sedentary elderly persons
equate riboflavin intake by elderly persons (8,27). One study is too low, and/or
(44) found mean riboflavin intake of institutionalized and non- 2. calorie intake markedly decreased on weekends, when food
institutionalized elderly that was slightly below the 1989 RDA. intake was not measured.
Thiamin (B-I). Thiamin intake was adequate, and averaged
128.7% (enhanced) and 135.2% (unenhanced) of the RDA. This Improved Handgrip Strength
is consistent with other studies (10,27) that found thiamin intake
to be sufficient. One study found mean daily thiamin intake to Improved grip strength was evident after 3 weeks' consump-
be slightly below the 1989 RDA values (18). tion of flavor-enhanced foods (Table 4). However, grip strength
Vitamin A. Vitamin A intake was adequate and averaged remained below the average levels previously reported for persons
169.2% (enhanced) and 180.4% (unenhanced) of the RDA. This aged 75 and over (average age not indicated) (20). This may be
finding is consistent with previous reports (10,27). Even for per- attributable to a greater average age of the subjects in the present
sons with low dietary intake of vitamin A, deficiency is unlikely study, because Mathiowetz et al. (20) report a steep age-related
to be a problem, because hepatic storage of vitamin A allows decline in grip strength in persons over age 65. It is noteworthy
circulating levels to be maintained within a narrow range that subjects in the present study tended to have low dietary
(28,40,49). intake potassium intake, as a relationship has been found be-
Vitamin C. Intake of vitamin C was more than twice the tween decreased dietary potassium and a decline in hand-grip
RDA, averaging 205.4% (enhanced) and 221.8% (unenhanced) strength, despite serum potassium levels within normal range (17).
of the RDA. Intake of vitamin C in the elderly is generally ad-
equate (9,27,49), although dietary intake of vitamin C varies Dietary Recall in the Elderly
widely among elderly persons [reviewed by Suter and Russell
On three occasions subjects were asked to recall their intake
(40)]. Impaired absorption of vitamin C with aging was noted
in a study of hospitalized elderly persons (4). from the previous day. A review of these 24-h recalls indicated
that elderly subjects underestimated their intake by an average
Vitamin E. Vitamin E intake was more than twice the RDA,
of 273 calories, and these omitted calories were predominantly
averaging 214.8% (unenhanced) and 254.2% (enhanced) of the
RDA. Although one study found vitamin E intake to be adequate vegetables and meats, but not desserts. The elderly subjects in
this study had been recruited by the dietitian because they had
in free-living elderly (18), another report (10) found that over
50% of free-living men and women over the age of 60 had dietary complained that they were not interested in eating. This finding
intake of vitamin E below the RDA. of underestimation of intake may explain why elderly in this
study were not as malnourished as expected by the dietitian.
Relationship Between Dietary Intake and Body Status of
Micronutrients and Energy SUMMARY AND CONCLUSIONS
The level of dietary intake of a nutrients is often, but not In summary, flavor enhancement of food for elderly retire-
invariably, correlated with bodily nutritive status. Nutrients for ment-home residents resulted in increased food intake and im-
which correlations were found previously in the literature be- proved immune status. An additional improvement in well being
tween dietary intake and circulating levels in elderly persons that resulted from food flavor enhancement was increased grip
include beta-carotene, alpha-tocopherol, zinc, riboflavin, pyri- strength in both hands. Dietary deficiencies in calcium, copper,
doxin, and vitamin C (16). However, dietary intake of retinol, magnesium, pantothenic acid, potassium, selenium, and zinc
thiamin, folic acid, cobalamin (11,12,16,49) did not correlate were found in both the enhanced and unenhanced conditions.
with circulating levels of these nutrients.
The discrepancy between adequacy of nutritional status as ACKNOWLEDGEMENTS
assessed by dietary intake and adequacy as measured by blood
Supported in part by NIA AG00443 and the Flavor and Extract
assay may reflect one or more of the unresolved issues associated Manufacturers' Association. Dr. Connie Bales and Dr. Susan Swithers-
with nutritional assessment. Mulvey are thanked for their comments on this paper.
REFERENCES
1. Bobroff, E. M.; Kissileff, H. R. Effects of changes in palatability on 3. Chumlea, W. C.; Roche, A. F,; Mukherjee, D. Nutritional assessment
food intake and the cumulative food intake curve in man. Appetite of the elderly through anthropometry. The Ross Medical Nutritional
7:85-96; 1986.
System. Columbus, OH: Ross Laboratories; 1984.
2. Bunker, V. W.; Hinks, L. J.; Lawson, M. S.; Clayton, B. E. Assessment 4. Davies, H. E. F.; Davies, J. E. W.; Hughes, R. E.; Jones, E. Studies
of zinc and copper status of health elderly people using metabolic on the absorption of 1-xyloascorbicacid (vitamin C) in young and
balance studies and measurement of leucocyte concentrations. Am. elderly subjects. Hum. Nutr. Clin. Nutr. 38C:436-71; 1984.
J. Clin. Nutr. 40:1096-1102; 1984. 5. Drewnowski, A.; Krahn, D. D.; Demitrack, M. A.; Nairn, K.; Gosnell,
402 S C H I F F M A N A N I ) ~,~,\RWICK
B. A. Taste responses and preferences for sweet high-tat tbods: Ev- 28. Saito, M.; Itoh, R. Nutritional status of vitamin A in a healthy pop-
idence for opioid involvement. Physiol. Behav. 51:371-379:1992. ulation in Japan. Int. J. Vit. Nutr. Res. 61:105-109; 1991.
6. ESHA Research. The food processor II user's manual. Salem, OR: 29. Sandstead, H. H.; Dintzis, F. R.: Bogyo, T. P.: Milne, D. A.: Jacob,
1987. R. A.: Klevay, L. M. Dietary, factors that can impair calcium and
7. Fantino, M.: Hosotte, J.; Apfelbaum, M. An opioid antagonist, nal- zinc nutriture of the elderly. In: Prinsley, D. M.: Sandstead, H. H.,
trexone, reduces preference for sucrose in humans. Am. J. Physiol. eds. Nutrition and aging. New York: Alan R. l~iss, lnc: 1990:241-
25 I:RgI-R96: 1986. 262.
8. Garry, P. J.: Goodwin, J. S.; Hunt, W. C. Nutritional status in a 30. Schiffman, S. S. Changes in taste and smell with age: Psychophysical
healthy elderly population: Riboflavin. Am. J. Clin. Nutr. 36:902- aspects. In: Ordy, J. M.: Brizzee, K., eds. Sensory systems and com-
909; 1982. munication in the elderly (A~,in~,,. Vol. IO) New York: Raven Press:
9. Garry, P. J.; Goodwin, J. S.; Hunt, W. C.; Gilbert, B. A. Nutritional 1979:227-246.
status in a healthy elderly population: Vitamin C. Am. J. Clin. Nutr. 31. Schiffman, S. S. Taste and smell in disease. N. Eng. J. Med. 308:
36:332-339; 1982. 1275-1279; 1983.
10. Garry,, P. J.; Goodwin, J. S.; Hunt, W. C.: Hooper, E. M.; Leonard, 32. Schiffman, S. S. Smell. In: Maddox, G. L.. ed. Encyclopedia of aging.
A. G. Nutritional status in a healthy elderly population: Dietary and New York: Springer; 1987:618-619.
supplemental intakes. Am. J. Clin. Nutr. 36:319-331; 1982. 33. Schiffman, S. S. Taste. In: Maddox, G. L., ed. Encyclopedia of aging.
1I. Garry, P. J.; Goodwin, J. S.; Hunt, W. C. Folate and vitamin B-12 New York: Springer; 1987:655-658.
status in a healthy elderly population. J. Am. Geriatr. Soc. 32:719- 34. Schiffman, S. S.: Pasternak, M. Decreased discrimination of tood
726: 1984. odors in the elderly. J. Gerontol. 34:73-79; 1979.
12. Gibson, R. S.; Martinez, O. B.; McDonald, A. C. The zinc, copper, 35. Schiffman, S. S.: Warwick, Z. S. Flavor enhancement of foods for
and selenium status of a selected sample of Canadian elderly women. the elderly can reverse anorexia. Neurobiol. Aging 9:24-26: 1988.
J. Gerontol. 40:296-302; 1985. 36. Schiffman, S. S.; Crumbliss, A. L.; Warwick, Z. S.; Graham, B. G.
13. Goodwin, J. S.; Garry, P. J. Lack of correlation between indices of Thresholds for sodium salts in young and elderly subjects: Correlation
nutritional status and immunologic function in elderly humans. J. with molar conductivity of the anion. Chem. Senses 15:671-678:
Gerontol. Med. Sci. 43:M46-M49; 1988. 1990.
14. Heaney, R. P.; Gallagher, J. C.; Johnston, C. C.: Neer, R.; Parfitt, 37. Schifl'man, S. S.: Warwick, Z. S. Changes in taste and smell over
A. M.: Chir, B.: Whedon, G. D. Calcium nutrition and bone health the tifespan: Effects on appetite and nutrition in the elderly. In:
in the elderly. Am. J. Clin. Nutr. 36:986-1013: 1982. Friedman, M. [.: Tordoff, M. G.; Kare, M. R., eds. Chemical senses,
15. Helgeland, K.: Haider, T.; Jonsen, J. Copper and zinc in human vot. 4. Appetite and nutrition. New York: Marcel Dekker; 1991:
serum in Norway: Relationship to geography, sex and age. Scand. 341-365.
J. Clin. Lab. Invest. 42:35-39; 1982. 38. Solomon, G. F.: Fiatarone, M. A.; Benton, D.; Morley, J. E.; Bloom,
16. Herbeth, B.: Chavance, M.; Musse, N.; Mejean, L.: Vernhes, G. E.: Makinodan, T. Psychoimmunologic and endorphin function in
Dietary intake and other determinants of blood vitamins in an elderly the aged. Ann. NY Acad. Sci. 521:43-58; 1988.
population. Eur. J. Clin. Nutr. 43:175-186; 1989. 39. Srinivasan, V.; Christensen, N.; Wyse, B. W.; Hansen, R. G. Pan-
17. Judge, T. G.: Cowan, N. R. Dietary potassium intake and grip tothenic acid nutritional status in the elderly--lnstitutionalised and
strength in older people. Gerontol. Clin. 13:221-226; 1971. noninstitutionalised. Am. J. Clin. Nutr. 34:1736-1742; 1981.
40. Suter. P. M.; Russell, R. M. Vitamin nutriture and requirements of
18. Leiehter, J.; Angel, J. F.; Lee, M. Nutritional status of a select group
the elderly. In: Munro, H. N.; Danford, D. E,, eds. Nutrition, aging,
of free-living elderly people in Vancouver. CMA J. 118:40-43: 1978.
and the elderly. New York: Plenum Press; 1989:245-291.
19. Lynch, S. R.; Finch, C. A.; Monsen, E. R.: Cook, J. D. Iron status
41. Swanson, C. A.; Mansourian, R.; Dirren, H.; Rapin, C. H. Zinc
of elderly Americans. Am. J. Clin. Nutr. 36:1032-1045; 1982.
status of healthy elderly adults: Response to supplementation. Am.
20. Mathiowetz, V,; Kashman, N.; Volland, G.: Weber, K.; Dowe, M.; J. Clin. Nutr. 48:343-349; 1988.
Rogers, S. Grip and pinch strength: Normative data for adults. Arch. 42. Thomas, P. D.; Goodwin, J. M.; Goodwin, J. D. Effect of social
Phys. Med. Rehabil. 66:69-74; 1985. support on stress-related changes in cholesterol level, uric acid level,
21. Mertz, W.; Morris, E. R.; Smith, J. C., Jr.; Udomkesmalee, E.; Fields, and immune function in an elderly sample. Am. J. Psychiat~ 142:
M.: Levander, O. A.; Anderson, R. A. Trace elements in the elderly: 735-737: 1985.
Metabolism, requirements, and recommendations for intakes. In: 43. Yolonen, M.; Halme, M.; Sarna, S. Vitamin E and selenium sup-
Munro, H. N.; Danford, D. E., eds. Nutrition, aging, and the elderly. plementation in geriatric patients. Biol. Trace Elem. Res. 7:161-
New York: Plenum Press; 1989:195-244. 168; 1985.
22. Monneuse, M. O.; Bellisle, F.; Louis-Sylvestre, J. Responses to an 44. Vir, S. C.; Love, A. H. G. Nutritional status of institutionalized and
intense sweetener in humans: Immediate preference and delayed noninstitutionalized aged in Belfast, Northern Ireland. Am. J. Clin.
effects on intake. Physiol. Behav. 49:325-330; 1991. Nutr. 32:1934-1947; 1979.
23. Munro, H. N.: McGandy, R. B.: Hartz, S. C.; Russell, R. M.; Jacob, 45. Walsh, J. H.; Wyse, B. W.; Hansen, R. G. Pantothenic acid content
R. A.: Otradovec, C. L. Protein nutriture of a group of free-living of a nursing home diet. Ann. Nutr. Metab. 25:178-181 : 1981.
elderly. Am. J. Clin. Nutr. 46:586-592: 1987. 46. Warwick, Z. S.: Schiffman, S. S. Palatability and nutrient effects on
24. Nguyen, N. H.; Flint, D. M.; Prinsley, D. M.; Wahlqvist, M. L. postprandial satiety. First annual meeting of the society for the study
Nutrient intakes of dependent and apparently independent nursing of ingestive behavior, Princeton, N J; June 1992.
home patients. Hum. Nutr. Appl. Nutr. 39A:333-338; 1985. 47. Woo, J.; Cheung, C. K.; Ho, S. C.; Mak, Y. T.; Swaminathan, R.
25. Recommended daily allowances, 10th ed. Washington DC: National Protein nutritional status in elderly Chinese in Hong Kong. Eur. J.
Academy Press; 1989. Clin. Nutr. 42:903-909: 1988.
26. Reid, L. D. Endogenous opioid peptides and regulation of drinking 48. Woody, E. Z.; Costanzo, P. R.; Liefer, H.; Conger, J. The effects of
and feeding. Am. J. Clin. Nutr. 42:1099-1132; 1985. taste and caloric perceptions on the eating behavior of restrained
27. Sahyoun, N. R.; Otradovec, C. L.; Hartz, S. C.; Jacob, R. A.; Peters, and unrestrained subjects. Cog. Ther. Res. 5:381-390; 1981.
H.: Russell, R. M.: McGandy, R. B. Dietary intakes and biochemical 49. Yearick, E. S.; Wang, M. S. L.; Pisias, S. J. Nutritional status of the
indicators of nutritional status in an elderly, institutionalized pop- elderly: Dietary. and biochemical findings. J. Gerontol. 35:663-671:
ulation. Am. J. Clin. Nutr. 47:524-533: 1988. 1980.