HEC PRESS Publisher of the
Healthy Eating Club website &
A
sia Pacific Journal of Clinical Nutrition

 


Volume 16 (2007)
1 Issue 1
1 Issue 2
1 Issue 3
1 Issue 4
1 Supplement 1
1 Supplement 2
Volume 15 (2006)
Issue 1
Issue 2
Issue 3
Issue 4
Supplement
Nutrition Society of Australia
Volume 14 (2005)
Issue 1
Supplement on CD
IUNS/APCNS proceedings
Issue 2
Issue 3
Issue 4
Supplement
Nutrition Society of Australia
CURRENT YEAR ISSUES
LOGIN to FULL PAPERS
subscribers only
PAST ISSUES
View full papers (free)
CD-Rom AU$190 vol1-13
NUTRITION SOCIETY OF AUSTRALIA 1976-
View Abstracts
Search our site
 
1000 Asia Pacific J Clin Nutr (1996) 5: 79-83

Asia Pacific J Clin Nutr (1996) 5: 79-83

Body mass index of the elderly derived from height and from armspan

B Rabe1,2 MSc, MH Thamrin1 MD, R Gross2,3 PhD, NW Solomons4 MD, W Schultink3 PhD

  1. SEAMEO-TROPMED Regional Center on Community Nutrition, University of Indonesia, Jakarta
  2. Institute for Nutritional Sciences, University of Bonn, Bonn, Germany;
  3. Deutsche Gesellschaft fÜ r Technische Zusammenarbeit (GTZ) Eschborn, Germany
  4. Center for Studies of Sensory Impairment, Aging and Metabolism (CeSSIAM), Guatemala City, Guatemala

The body mass index (BMI) has been promoted as a useful indicator for chronic energy deficiency, and to a lesser extent to indicate obesity. For the growing sector of elderly in developing countries, such as Indonesia, both issues are taking on public health relevance. The aging process leads to a progressive loss of height, and questions have been raised as to the appropriate value to include in the denominator of the BMI formula, WT(kg)/HT(m2), when applied in this age-group. The armspan has been advanced as a surrogate for height, correcting for the lifelong loss of stature. In a data-set from 69 elderly in Indonesia, 36 women and 33 men, aged 60 to 69 y, we have examined the interrelationships of height and armspan. The correlation coefficient for the regression of the two measures were r = 0.83 and r = 0.81 (p < 0.001), for women and men, respectively.

Substituting the armspan term in the denominator to compose a Body Mass using Armspan (BMA) Index, we observe for this population a 32% increase in estimates for Chronic Energy Deficiency (CED) for women and 24% increase in estimates of CED for men. Corresponding estimates for obesity rates declined by 45% and 81% respectively. The senescent changes in stature raise important questions for our capacity to estimate prevalences of body composition disorders in the older population.


Introduction

Poor nutritional status is common among the elderly, and is associated with increased mortality and morbidity1,2. Yet, until recently, there has been little research on the nutritional status of the elderly3. Aging is accompanied by changes in body composition and stature4. Furthermore, racial differences have been reported in anthropometric indices5-8, making the analysis of nutritional status in elderly more complex and discouraging.

Numerous methods are available to assess nutritional status by way of body composition, also applicable for the elderly9,10. Body mass index (BMI) has usually been the index of choice in studies, because its components - height and weight - are rapid and simple to measure. The robustness of the BMI as an indicator of chronic energy deficiency (CED) has been vigorously championed8,11,12, and, to a lesser extent, defended as an index of overweight as well12-14. Furthermore both extremes of BMI have proven to be strong predictors of increased mortality and morbidity15-17.

Functional decline is a reality for the elderly18 and the superimposition of age and CED would be expected to compound an adverse situation. How well, we might ask, does the BMI serve as a predictor of CED in those of advanced age, and are the cut-off points proposed in the classification applicable for the elderly? Using height in calculating BMI could be inappropriate because of height-loss with aging due to the compression of vertebrae, kyphosis and osteoporosis19-21. Solomons et al22 have raised the question of an appropriate weight to cover a frame in which the vertical dimension (height) is shrinking. Correction of the measured height by an estimate of the stature that existed in young adulthood was suggested23. It might be that by using height in calculating BMI the prevalence of CED in elderly is under-estimated. Armspan is relatively independent of aging and is highly related to the height of an individual23. Therefore, to predict the prevalence of CED in elderly it may be more reliable to use armspan in the determination of weight related to body stature.

Asian populations are notable for their low BMIs, putatively reflecting risk of CED24. Thus, the aim of the present study was to examine the nutritional status of the elderly by measuring BMI, and then substituting the armspan term for the BMA. We also examine the level of correspondence between the two measures (armspan and stature) in Indonesian elderly, providing novel information on the body composition of the older population in urban Jakarta.

Materials and methods

The study was carried out in the community of Kelurahan Kemayoran, a low income area in Central Jakarta, Indonesia during April/May 1993. The elderly were selected by simple random sampling out of community lists. If somebody had moved away or died, or could not be located after trying twice, another elderly person of the same sex and from the same subdistrict of Kelurahan Kemayoran was chosen.

In the collection of the anthropometric data, weight, height and armspan measurements were taken after standardising of the examiner. The subjects were measured barefoot with light-weight clothing. Body weights were recorded with an exactness of 0.1 kg using SECA digital weighing scale (Hamburg, Germany). To measure height, the barefoot subjects were requested to stand straight on a horizontal surface, heels together, the eyes straight forward. The height measuring equipment consisted of a microtoise fixed to the wall. Armspan was measured in the same position as the height, but with the extended arms in a 90° angle to the body, using a flexible tape. It was measured across the chest from the longest finger of the left hand to the longest finger of the right hand. Three readings were taken for each measurement and the median has been taken as the representative value. Two indices of nutritional status were used: Body Mass Index (BMI), or weight/height2 (kg/m2), and Body Mass Index using armspan (BMA), weight/armspan2 (kg/m2). The classification 1000 of James et al8 was used for identification of CED.

Table 1. Age and selected anthropometric data of a group of elderly females and males from Jakarta Indonesia (mean, standard deviation and range).

 

Females (n=36)

Males (n=33)

 

Mean

SD

Range

Mean

SD

Range

Age

64.6

± 2.9

60-69

63.6

± 2.9

60-69

Weight (kg)*

46.7

± 10.2

30.2-70.4

52.9

± 10.5

32.1-75.9

Height (cm)**

146.8

± 4.7

136.1-154.3

157.9

± 5.7

143.0-166.3

AS (cm)**

154.0

± 6.0

141.2-164.0

165.7

± 6.8

152.1-176 8

HT/AS

0.96

± 0.05

0 9-1.01

0.95

± 0.06

0.84-1.02

BMI (kg/m2)

21.7

± 4.7

14.3-30.2

21.3

± 4.2

13.8-30.0

BMA (kg/m2)

19.7

± 4.3

13.5-26.8

19.3

± 3.8

11.6-27.7

The International Guidelines for Ethical reviews of Epidemiological Studies25 served as a basis for the ethical considerations of the implementation of this study. For the statistical analysis first, the distribution of all variables were tested against a normal distribution using the Kolomogrov-Smirnov Test to check for differences at a significance level of p < 0.05. Differences in mean values between sexes were analysed using Student’s t-test for independent samples with a confidence interval of 95% (p,<0.05). Correlation analysis of anthropometric variables was carried out to calculate the Pearson product - moment correlation coefficient.

Results

Sixty-nine subjects, 36 women and 33 men aged 60 to 69 y, were examined. Table 1 lists sex-specific means, standard deviations and ranges of the age and anthropometric measurements for the subjects. Women had significa 1000 ntly lower weight, height and armspan than men (p < 0.05). No significant differences between sexes were found for the height/armspan-relationship (HT/AS), the BMI and the BMA.

On average the armspan of the females was 7.3 cm longer than height; that of the males was 7.6 cm longer (Table 2). The range of difference between armspan and height was wide, from -2.4 cm up to 17.0 cm in both genders. The BMA was, on average, 2.0 kg/m2 lower than the BMI for both sexes on average.

Figures 1 and 2 show the correlation coefficients of the linear regression between armspan and height, for females (0.83) and males (0.81), respectively; their significance was p<0.001. A similar statistical significance was observed for the relation between the BMI and the BMA; the correlation coefficients of the latter were 0.98 for women and 0.96 for men (Figures 3 and 4).

Table 2. Difference between armspan and height and between BMA and BMI in a selected group of elderly males and females from Jakarta.
Group

N

Mean

SD

Range

AS - HT (cm)        
All

69

7.9

± 4.0

-2.4-17.0

Women

36

7.3

± 3.3

-0.9-16.7

Men

33

7.6

± 3.6

-2.4-17.0

BMA - BMI (kg/m2)  

 

 
   
All

69

2.0

± 1.0

-0.7-6.1

Women

36

2.0

± 0.9

-0.2-4.3

Men

33

2.0

± 1.2

-0.7-6.1

AS - Armspan; HT - Height; BMI - Body mass index; BMA - Body mass index calculated by height

Figure 1. Correlation between height and armspan in a selected group of elderly females from Jakarta.
Figure 2. Correlation between height and armspan in a selected group of elderly males from Jakarta.
Figure 3. Correlation between BMI and BMA in a selected group of elderly females from Jakarta
Figure 4. Correlation between BMI and BMA in a selected group of elderly males from Jakarta.

Figures 5 and 6 show the proportion of the elderly falling into the different classes of chronic energy deficiency and obesity, for females and males, respectively. About one-third of the subjects had a BMI below 18.5 kg/m2. A remarkably high proportion of the male subjects (12%) had a BMI below 16.0 kg/m2 which is remarkably high, just as the percentage of females (17%) below the value of 17.0 kg/m2. Thirty-nine percent of the females and 46% of the males had a nutritional status considered to be normal. Thirty-one percent of the female subjects and 21% of the male subjects were obese. Using the armspan instead of the height calculating the body mass using armspan (BMA), 46% of the elderly were classified as undernourished. The portion of the elderly with a BMA of < 16.0 kg/m2 became especially high at 27%. No elderly were classified as obese using BMA (>= 30).

Figure 5. Distribution of body mass index BMI of a selected group of elderly females and males from Jakarta according to the classification of James et al8 and Garrow and Websterl4.
Figure 6. Distribution of body mass index calculated by armspan (BMA) of a selected group of elderly females and males from Jakarta according to the classification of James et al8 and Garrow and Webster14.

Discussion

Indonesian elderly in this sample are dramatically smaller and lighter than their American counterparts26. The difference in mean height between Indonesian and American subjects was 20 kg for both sexes. Furthermore the mean values of BMI in this study were found to be lower than those of developed countries. The EC/EURONUT SENECA Study, which assessed representative samples aged 75 to 81 in 12 European countries27, found a range in mean values of BMI from 23.9 to 30.5 kg/m2 for women, and from 24.4 to 30.3 kg/m2 for men. Our mean BMIs of 21.7 kg/m2 for females and 21.3 kg/m2 for males, were below the lowest mean BMIs of any European subsample. These findings support those of other studies, which found that small stature as well as low body weight, seems to be more common in developing countries than in developed countries5,12. Reasons for differences have been suggested to have genetic or environmental bases5,28-30. Furthermore, racial differences in the relationship between body composition and BMI have been reported6-8. Because BMI reflects body fat mass as well as lean body mass, the same BMI can represent a completely different body composition in different races. Therefore, comparison between different populations have to be viewed cautiously.

James et al8 proposed a classification with three cut-off points for Chronic Energy Deficiency (CED). Low values of BMI reflect low 1000 fat and lean-body masses, a state of greater concern than low fat mass alone, and are perhaps more typical of Chronic Energy Deficiency than low fat mass alone5. Values below 18.5 kg/m2 were in general considered as incompatible with normal good health6,8; values below 17.0 kg/m2 were found to be related to evidence of poor productivity, and increased morbidity and mortality. With values below 16.0 kg/m2, the mortality risk increased progressively. This is of great concern because values outside the range considered as normal have been shown to be incompatible with health. Grade III of CED, (10% of the subjects) showed a tripling of mortality rates compared to the normal range - a situation demanding special attention. Grade II of CED has been related to an increasing evidence of poor productivity, and increased morbidity and mortality8. The finding that 31% of female subjects and 21% of the males were classified as obese is also of concern because obesity classified by BMI has been established as a risk factor of morbidity and mortality16,31,32. These results have to be judged carefully. Although the classification of James et al8 was based on findings of developing countries, the anthropometric data were derived from adults aged 20 to 45 y. However, mean values of BMI have been reported to decrease with aging6 and it is clear that values in the elderly Indonesians are low (although we do not have a young adult population from Jakarta which with to assess age-related trends).

On the other side of the BMI equation, cut-off points for obesity correspond in their classification to the grades of obesity of Garrow and Webster14: 25.0 to 29.9 kg/m2 (Grade I - as overweight); 30.0 to 39.9 kg/m2 (Grade II - as obese); and ³ 40.0 kg/m2 (Grade III - or morbid obesity). As shown in Figures 5 and 6, in the upper panels, a parallel percentage of women, 32 and 31%, respectively, had some degree of CED or obesity, with none of the latter in the Grade III extreme. For men, the rates of all classes of obesity, at 21% was only two-thirds of their respective rate of underweight.

The high correlation between height and armspan of 0.83 for females and 0.81 for males, found in this sample of Indonesian elderly, confirmed that armspan approximates the same rank-ordering of a population as height. Although aging could have produced differential effects on stature in different people, some greater disordering of the relationship between the two measures might have developed. In a cross-sectional study such as this (and without a representative young-adult control population), however, it could not be determined how much these relationships were the original ones of youth or the weaker relationship in the aged due to irregular height decrease. Height/armspan ratio racial differences have been reported, too33, but the population of this section of Jakarta were largely Javanese.

According to the classification system of James et al8, about one-third of the examined female and male subjects had CED whereas a little less than one-third of the elderly were obese. A comparison of the upper and lower panels in the Figures 5 and 6, reveals visually the effect of substituting armspan in the denominator of the body mass index formula. The total percentage of the female population in some stage of chronic energy deficiency would rise from 32 to 47% if armspan is, indeed, a more valid representation of the biologically relevant length of an older, shortened individual. Estimates of obesity of any grade, on the other hand falls from 31 to 17% in this gender. For men, the proxy use of armspan raises the overall apparent CED prevalence from 33 to 42%, while lowering that of o 1000 besity from 21 to 3%.

If we were concerned about a high degree of CED in this aging urban Indonesian population based on the BMI pattern based on height, while also worrying about abnormal overweight, as well, the substitution of the armspan in the denominator should tranquillise us with respect to the latter and truly alarm us with regard to the former. Recent unpublished work in Guatemala34, that at least for that Central American population, the height/armspan index in young adulthood is not 1.00. It is slightly less in women and substantially less in men. Thus, the BMA would cause an overcorrection to the left of the BMI distribution. Given the ethnic differences in the relationship of height to armspan, the reference height/armspan ratio of youth should be established for each geographic region of interest.

In conclusion, extended longevity make the nutrition of the elderly, and residents in urban areas allows for a two-way concern for nutritional imbalance: under- and over-nutrition. Conceptual advances for the use of a the simplest of all body compositions indices, the body mass index, have been offered12, but their applicability in the elderly must be tested. We have confirmed here in a group of older residents of slum area in Jakarta the previously reported close correlation of the armspan and the height. It is still conjectural whether the armspan is a more valid indicator of the appropriate length of an older person who might have suffered senescent and pathological shortening of stature by the seventh decade22. Our study illustrates the magnitude of the deviation in the distribution that would occur if the armspan is indeed a better term. Furthermore, more research is needed on the functional consequences of low BMI and BMA in elderly.


Chinese abstract

Indonesian abstract


References

  1. Bastow MD, Rawling J, Allison SP. Undernutrition, hypothermia and injury in elderly women with fractured femur: an injury response to altered metabolism. Lancet 1983; i: 143-146.
  2. Bowman BB, Rosenberg IH. Assessment of the nutritional status of the elderly. Am J Clin Nutr 1982; 35: 1142-1151.
  3. Kucmarski RJ. Need for body composition information in elderly subjects. Am J Clin Nutr 1989; 50:1150-1157.
  4. Stoudt HW. The anthropometry of the elderly. Hum Factos 1981; 23: 29-36.
  5. Norgan NG. Body mass index and body energy stores in developing countries. Eur J Clin Nutr 1990; 44:79-84.
  6. Strickland SS, Ulijaszek SJ. Body mass index ageing and different reported morbidity in rural Sarawak. Eur J Clin Nutr 1993; 47:9-19.
  7. Wang J, Thornton JC, Russell M, Burastero S, Heymsfield S, Pierson RN Jr. Asians have lower body mass index (BMI) but higher percent body fat than do whites: comparison of anthropometric measurements. Am J Clin Nutr 1994; 60:23-28.
  8. James WPT, Ferro-Luzzi A, Waterlow JC. Definition of chronic energy deficiency in adults; report of a working paper of the International Dietary Energy Consultative Group. Eur J Clin Nutr 1988; 42:969-981.
  9. Lukaski HC. Methods for the assessment of human body composition: traditional and new. Am J Clin Nutr 1987; 46:537-556.
  10. Deurenberg P. Assessm 1000 ent of body composition: Uses and misuses. Annual Report 1992. Nestle Foundation for the study of the Problems of Nutrition in the World. Laussane, Switzerland: Nestle Foundation 1993; 35-72.
  11. Ferro-Luzzi A, Sette S, Franklin M. James WPT. A simplified approach of assessing adult chronic energy deficiency. Eur J Clin Nutr. 1992; 46: 173-86.
  12. Shetty P, James WPT. Body mass index: a measure of chronic energy deficiency in adults. Food and Nutrition Paper No. 56. Rome: Food and Agriculture Organization, 1994.
  13. Norgan NG, Ferro-Luzzi A. Weight-height indices as estimates of fatness in men. Hum Nutr Clin Nutr 1992; 360:363-72.
  14. Garrow JS, Webster J. Quetelet’s Index (W/H2) as measure of fatness. Int J Obesity 1985; 9:147-153.
  15. Harris T, Cook EF, Garrison R Higgins MS, Kannel W, Goldman L. Body mass index and mortality among nonsmoking older persons. The Framingham Heart Study. JAMA 1988; 259:1520-524.
  16. Goldbourt U, Medalie JH. Weight-height indices. Prev Soc Med 1974; 28:116-26.
  17. Henry JK. Body mass index and the limits of human survival. Eur J Clin Nutr 1990; 44:329-335.
  18. Rowe JW, Kahn RL. Human aging: Usual and successful. Science 1987; 237:143-149.
  19. Dequeker JV, Baeyens JP, Claessens J. The significance of stature as a clinical measurement of ageing. J Am Gerontol Soc 1969; 17:169-179.
  20. Mitchell CO, Lipschitz DA. Detection of protein-calorie malnutrition in the elderly. Am J Clin Nutr 1982; 35:398-406.
  21. Wahlqvist MI, Flint DM. Assessment of loss of height in elderly women. Eur J Clin Nutr 1988; 42:679-682.
  22. Solomons NW, Mazariegos Mt Mendoza I. Uses of anthropometry in the elderly in the field setting with notes on screening in developing countries. Asia Pac J Clin Nutr 1993; 2:15-23.
  23. McPherson R, Lancaster DR, Carrole JC. Stature changes with aging in Black Americans. J Gerontol 1978; 33:20-25.
  24. Baqui AH, Arifeen SE, Amin S, Black RE. Levels and correlates of maternal nutritional status in urban Bangladesh. Eur J Clin Nutr 1994; 48:349-357.
  25. Council for International Organizations of Medical Sciences. International guidelines for ethical review of epidemiological studies. CIOMS, Geneva, 1991.
  26. Chumlea W, Guo S. Equations for predicting stature in white and black elderly individuals. J Gerontol 1992; 47:M197-M203.
  27. de Groot PCPGM, van Staveren WA, Hautvast JGAJ. Euronut SENECA. Nutrition and the elderly in Europe. Eur J Clin Nutr 1991; 45 (suppl 3); 1-196.
  28. Durnin JVGA. Anthropometric methods of assessing nutritional status. In: Horwitz A. ed Nutrition in the elderly. Oxford : Oxford University Press 1989: 15-32.
  29. Forbes GB. Body composition: influence of nutrition, disease, growth, and aging. In: Shils ME, Young VR, eds. Modern Nutrition in Health and Disease. Philadelphia: Lea & Febiger 1988: 533-556.
  30. Himes JH, Mueller WH. Age-associated statural loss and socio-economic status. J Am Geriatrics Soc 1977; 25:171-174.
  31. Gordon T, Kannel WB. The effects of 6ff overweight of on cardiovascular diseases. Geriatrics 1937; 28:80-85.
  32. Stevens J, Keil JE, Rust PF, Verdugo RR, Davis CE, Tyroler HA, Graves PC. Body mass index and body girths as predictors of mortality in Black and White men. Am J Epidem 1992; 135:1137-1146.
  33. Steele MF, Mattox JW. Short Report: Correlation of arm-span and height in young women of two races. Ann Hum Biol 1987; 14:445-447.
  34. Sengel JS, Schlimbach A, Solomons NW. unpublished; 1993.

to the top
       
next article


Copyright © 1996 [Asia Pacific Journal of Clinical Nutrition]. All rights reserved.
Revised: January 19, 1999 .

0