| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
Original Research Communication |
1 From the Obesity Research Center, St Luke’s–Roosevelt Hospital and the Institute of Human Nutrition, Columbia University, College of Physicians and Surgeons, New York (JK, ZW, SBH, and DG); the Department of Biobehavioral Sciences, Teachers College, Columbia University, New York (JK); and the Department of Internal Medicine, School of Medicine, University of New Mexico, Albuquerque (RNB).
2 Supported by National Institutes of Health grants R29-AG14715 and PO1-DK 42618.
3 Reprints not available. Address correspondence to D Gallagher, Obesity Research Center, 1090 Amsterdam Avenue, New York, NY 10025. E-mail: dg108{at}columbia.edu.
 |
ABSTRACT |
|---|
 TOP ABSTRACT INTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Objective: The objective was to develop prediction models linking ALST estimated by dual-energy X-ray absorptiometry (DXA) with total-body SM quantified by multislice magnetic resonance imaging in healthy adults.
Design: ALST and total-body SM were evaluated with a cross-sectional design in adults [body mass index (in kg/m2) < 35] with an SM-prediction model developed and validated in model-development and model-validation groups, respectively. The model-development and model-validation groups included 321 and 93 ethnically diverse adults, respectively.
Results: ALST alone was highly correlated with total-body SM (model 1: R2 = 0.96, SEE = 1.63 kg, P < 0.001), although multiple regression analyses showed 2 additional predictor variables: age (model 2: 2-variable combined R2 = 0.96, SEE = 1.58 kg, P < 0.001) and sex (model 3: 3-variable combined R2 = 0.96, SEE = 1.58 kg, P < 0.001). All 3 models performed well in the validation group. An SM-prediction model based on the SM-ALST ratio was also developed, although this model had limitations when it was applied across all subjects.
Conclusion: Total-body SM can be accurately predicted from DXA-estimated ALST, thus affording a practical means of quantifying the large and clinically important SM compartment.
Key Words: Body composition • nutritional assessment • skeletal muscle mass • magnetic resonance imaging • dual-energy X-ray absorptiometry
|
INTRODUCTION |
|---|
|
TOPABSTRACTINTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
An alternative approach for measuring total-body SM is dual-energy X-ray absorptiometry (DXA), because DXA instruments are widely available and are relatively inexpensive; in addition, radiation exposure is minimal with this technique (2,6,7). DXA systems provide a measure of appendicular lean soft tissue (ALST), a fat- and bone mineral–free component that includes muscle and other components such as skin, tendons, and connective tissues (8–11). SM constitutes the largest fraction of ALST, and previous investigators proposed several models for predicting SM with DXA (7,8,12,13). The 2 main proposed models (8,12) are now recognized as being either inaccurate or of limited applicability because of model imprecision or because of the complexity of the required measurements and calculations. These 2 models were reported before the availability of reference methods for measuring total-body and regional SM mass on large and diverse subject populations such as those now provided by MRI (1).
A large proportion of total-body SM is found in the extremities, and a large proportion of ALST is SM (Figure 1
). Therefore, DXA potentially affords a practical and available means for quantifying total-body SM mass. The aim of the present study was to develop and subsequently validate a total-body DXA SM-prediction model with the use of MRI as the reference method.
|
|
SUBJECTS AND METHODS |
|---|
|
TOPABSTRACTINTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Subjects
Subjects were healthy men and women aged 
18 y with a body mass index (BMI; in kg/m2) < 35 who had participated in previous multiethnic investigations of body composition (15). The subjects were recruited over 5 y through advertisements in newspapers, on radio stations, and in flyers posted in the local community. To be eligible for inclusion, the subjects had to be ambulatory and have no orthopedic problems that could affect any of the variables under investigation. Persons who regularly participated in vigorous physical activity training programs were excluded. Each subject completed a medical examination that included screening blood tests. Only healthy subjects with no diagnosed medical conditions were enrolled in the study. The study was approved by the Institutional Review Board of St Luke’s–Roosevelt Hospital Center, and all subjects gave written consent before participating.
Body-composition analysis
Body mass and height were measured to the nearest 0.1 kg and 0.5 cm with a digital scale (Weight Tronix, New York) and wall-mounted stadiometer (Holtain, Crosswell, United Kingdom), respectively.
Dual-energy X-ray absorptiometry
Whole-body and regional body composition were estimated by using DXA (software version 3.6; Lunar DPX, Madison, WI). The system software provided the mass of lean soft tissue, fat, and bone mineral for both the whole body and specific regions. ALST mass was considered equivalent to the sum of lean soft tissue in both the right and left arms and legs. Appendages were isolated from the trunk and head by using DXA regional computer-generated default lines, with manual adjustment, on the anterior view planogram. With the use of specific anatomic landmarks, the legs and arms were defined by this method as the soft tissue extending from a line drawn through and perpendicular to the axis of the femoral neck and angled with the pelvic brim to the phalange tips and the soft tissue extending from the center of the arm socket to the phalange tips, respectively. Repeated daily measurements over 5 d in 4 subjects showed a CV (100% x SD/mean) of 1.7% for leg lean soft tissue, 2.0% for arm lean soft tissue, and 2.6% for ALST (16). DXA was also used to provide descriptive measures of total-body fat across the 2 subject groups.
Magnetic resonance imaging
Total-body SM mass was measured by using whole-body multislice MRI as reported by Ross (14). Subjects were placed on the 1.5-T scanner (6X Horizon; General Electric, Milwaukee) platform with their arms extended above their heads. The protocol involved the acquisition of 
40 axial images across the whole body with 10-mm thickness and 40-mm intervals (14,17). Images were analyzed by using SliceOmatic image analysis software (TomoVision Inc, Montreal), and SM volume by MRI was converted to mass by using an assumed density of 1.04 kg/L for SM (18). The CV for repeated measurements of the same scan by the same observer of MRI-measured total-body SM volumes in our laboratory is 0.7% (17).
Statistical analysis
Differences in between-group characteristics were tested for statistical significance by using Student’s t tests. Pearson’s correlation coefficients were used to explore the associations between DXA-measured ALST and MRI-measured total-body SM in the model-development group. The simplest empirical SM-prediction model is SM = k x ALST, where k is the established ratio of SM to ALST. We therefore explored mean k values in men and women along with their respective SDs and CVs.
SM-prediction equations were first developed in the model-development group with the use of multiple linear regression analysis. Potential independent variables included ALST, age, sex, and race (African American, Asian, white, and Hispanic). Prediction equations were developed by stepwise multiple regression analysis with MRI-measured total-body SM set as the dependent variable. The adjusted R2 values were used to quantify model-fitting performance. In the next phase, the value for total-body SM mass was calculated for each subject in the validation group by using the developed prediction equations. Correlations were then explored between the predicted SM values and the corresponding actual values measured by MRI. The observed differences between predicted and actual total-body SM mass were tested for significance by using Student’s t tests, and the level of agreement was assessed according to the method of Bland and Altman (19). Data were analyzed by using SPSS version 8.0 (1997; SPSS Inc, Chicago), and statistical significance was set at P < 0.05. Group data are expressed as means ± SDs.
|
RESULTS |
|---|
|
TOPABSTRACTINTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
. There was no significant difference in BMI between the men (25.6 ± 3.6) and women (24.8 ± 4.3) in the model-development group, although men were heavier, taller, and younger than the women (all P < 0.001).
|
The total sample of 414 subjects was ethnically diverse across both groups: 139 African Americans, 48 Asians, 177 whites, and 50 Hispanics. The racial distribution (%) in the model-development group was as follows (men and women, respectively): 39 and 38 whites, 30 and 39 African Americans, 15 and 12 Hispanics, and 15 and 11 Asians. The racial distribution in the validation group was as follows (men and women, respectively): 58 and 57 whites, 16 and 33 African Americans, 12 and 6 Hispanics, and 16 and 4 Asians.
Prediction models
Model-development
Women had a greater MRI-measured total-body adipose tissue mass than did the men (22.3 ± 9.4 kg compared with 17.6 ± 7.2 kg, P < 0.001). Total-body adipose tissue mass was positively correlated with age in men (r = 0.33) and in women (r = 0.34) (both P < 0.001). The slope of the regression line between total-body adipose tissue and age was 0.14 ± 0.03 kg/y in the men and 0.17 ± 0.04 kg/y in the women (P < 0.001).
ALST (in kg) was the strongest predictor (P < 0.001) of total-body SM mass, explaining 95.7% of the between-subject variance in MRI-measured SM mass (in kg) in model 1 (Table 2 and Figure 2):
 | (1) |
|
|
):
 | (2) |
Sex (0 = female; 1 = male) was a borderline contributor to predicted total-body SM mass (P = 0.052), and the addition of race failed to contribute significantly (P = 0.42) to the developed model (model 3, Table 2):
 | (3) |
Model validation
The mean values and correlations between MRI-measured and model-predicted SM mass are presented in Table 3. Predicted total-body SM mass values derived from all 3 models did not differ significantly from measured SM mass. Predicted total-body SM mass was highly correlated (all r 0.96, P < 0.001) with measured SM mass for all 3 models. The addition of age and sex to ALST in the prediction models led to a small increase in the correlation between measured and predicted total-body SM mass (ie, from r = 0.96 to 0.97). A Bland-Altman analysis showed no significant between-method bias (eg, model 3, Figure 3).
|
|
|
DISCUSSION |
|---|
|
TOPABSTRACTINTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
SM-prediction models
SM-ALST ratio
Our first level approach was to explore the use of DXA-estimated ALST as the sole SM predictor (ie, SM = k x ALST). We based this strategy on 2 observations: that ALST is mainly muscle (76%) (15,20) and that a large proportion (74%) of total-body SM is in the extremities (Figure 1) (18). These observations indicate that ALST and total-body SM are 2 overlapping components and suggest that there may be a high correlation between the two. The results of the present study support this hypothesis (model 1: R2 = 0.96, SEE = 1.63 kg).
Rough estimates based on earlier reports (15,18,20) suggest a k value (ie, SM/ALST) of 1.0 (ie, 0.76/0.74 = 1.03). Our observed mean values for men (ie, k = 1.15) and women (ie, k = 1.13) were reasonably close to this estimated value, given the exigencies of defining the appendicular portion of body mass. However, we found in simple and multiple regression analyses that both sex and age moderate the relation between SM and ALST. After adjustment for ALST, women had a smaller SM mass than did men, and the elderly had a smaller SM mass than did young subjects. A smaller k value in women may be, in part, secondary to a larger adipose tissue contribution to ALST compared with men. Similarly, the smaller k value in the elderly may be secondary to a larger adipose tissue contribution to ALST compared with that observed in young subjects. ALST is composed of muscle, skin, connective tissue, and the lean portion of adipose tissue. In the aging process, SM decreases but other components such as connective tissue and the lean portion of adipose tissue increase. As a result, the SM-ALST ratio probably decreases during the aging process, as observed in our study.
An example of this age and sex effect on the SM-ALST ratio is as follows. Assuming that both SM and ALST are equal to 25 kg in men and young subjects, the corresponding ratio of SM to ALST would be 25/25 = 1.0. If we then assume the same SM mass for women and elderly subjects, there would be an appropriate increase in appendicular adipose tissue of 5 kg. About 20% of adipose tissue mass is lean soft tissue (ie, water and protein) and the remaining 80% is fat. Therefore, 5 kg adipose tissue includes 1 kg lean soft tissue. When body composition is determined with DXA, this 1 kg lean soft tissue is included in the ALST compartment. The corresponding ratio of SM to ALST is then 25/(25 + 1) = 0.96 for the women and elderly subjects. Women and elderly subjects thus have a smaller SM-ALST ratio than do men and young subjects with an equivalent appendicular SM mass.
Therefore, a simple proportionality SM-prediction model based on an assumed constant k value would not be very accurate (CVs for men and women: 5.2% and 7.1%, respectively), and the predicted SM values would also have an age and sex bias. However, this does not negate the possibility of using ALST per se as a surrogate body-composition marker of total-body SM mass, particularly because the R2 of SM versus ALST was 0.96 with an SEE of 1.63 kg.
Composite regression model
Accordingly, the final developed multiple regression model controlled for age and sex after adjustment for ALST (Table 2; model 3: R2 = 0.96, SEE = 1.58 kg). Race was not a significant predictor of SM after the 3 other predictor variables were controlled for. Because age and sex are easily acquired predictors, it is reasonable to apply this last model for clinical and research purposes. The low SEE for this model can be compared with the corresponding SM-prediction model SEEs for anthropometry (ie, 2.8 kg), bioimpedance analysis (ie, 2.7 kg), urinary 3-methyl histidine (ie, 2.3 kg), and urinary creatinine (ie, 1.9 kg) (5).
Study limitations
In the present study we applied the regional default option of DXA with manual adjustment to evaluate regional ALST mass. This approach was applied for practical reasons because most trained DXA technicians can obtain the data required for SM mass estimation. However, the possibility exists that even more specific regional appendicular anatomic landmarks can be developed. Moreover, our DXA system was purchased from Lunar Corporation, and we have no information on the comparability of regional estimates across instruments from different manufacturers.
A second proviso regarding the developed models is that the equations are population specific. The models would be inappropriate for use in body builders or in any group that differs substantially from the subjects evaluated in this report. Additionally, the models are not appropriate for use in younger age groups, and there remains a need to develop similar prediction formulas for use in children and adolescents.
A third limitation involves the assumed constant density of SM tissue of 1.04 kg/L (18). Variability in actual SM density may introduce a small error into the MRI-estimated SM.
Last, our models were developed in a cross-sectional cohort and similarly validated in a study group evaluated at only one time point. A need exists for establishing the validity of the models in longitudinally monitored populations, particularly those in whom interventions are part of the study protocol.
Conclusions
In summary, 3 new models for predicting total-body SM mass with the use of DXA were developed and then validated in a large sample of ethnically diverse, healthy, adult men and women. This observation suggests that the new DXA models can provide reliable and accurate estimates of total-body SM mass in adult populations. Further studies are needed to validate the models in other study populations and DXA systems and to evaluate the applicability of these developed formulas in longitudinal studies for the detection of change in SM mass in response to interventions.
|
REFERENCES |
|---|
|
TOPABSTRACTINTRODUCTIONSUBJECTS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
This article has been cited by other articles:
|
|
 |
|
  G. D. Summers, C. M. Deighton, M. J. Rennie, and A. H. Booth Rheumatoid cachexia: a clinical perspective Rheumatology, August 1, 2008; 47(8): 1124 - 1131. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 M.-P. St-Onge and A. Bosarge Weight-loss diet that includes consumption of medium-chain triacylglycerol oil leads to a greater rate of weight and fat mass loss than does olive oil Am. J. Clinical Nutrition, March 1, 2008; 87(3): 621 - 626. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. A. Allan, B. J. G. Strauss, H. G. Burger, E. A. Forbes, and R. I. McLachlan Testosterone Therapy Prevents Gain in Visceral Adipose Tissue and Loss of Skeletal Muscle in Nonobese Aging Men J. Clin. Endocrinol. Metab., January 1, 2008; 93(1): 139 - 146. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 Z. Chen, Z. Wang, T. Lohman, S. B. Heymsfield, E. Outwater, J. S. Nicholas, T. Bassford, A. LaCroix, D. Sherrill, M. Punyanitya, et al. Dual-Energy X-Ray Absorptiometry Is a Valid Tool for Assessing Skeletal Muscle Mass in Older Women J. Nutr., December 1, 2007; 137(12): 2775 - 2780. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C. A Clay, S. Perera, J. M Wagner, M. E Miller, J. B Nelson, and S. L Greenspan Physical Function in Men With Prostate Cancer on Androgen Deprivation Therapy Physical Therapy, October 1, 2007; 87(10): 1325 - 1333. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Z. Wang, S. Heshka, A. Pietrobelli, Z. Chen, A. M. Silva, L. B. Sardinha, J. Wang, D. Gallager, and S. B. Heymsfield A New Total Body Potassium Method to Estimate Total Body Skeletal Muscle Mass in Children J. Nutr., August 1, 2007; 137(8): 1988 - 1991. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. H. Macdonald, S. M. Marcora, M. J. Kumwenda, M. Jibani, G. Roberts, R. Glover, J. Barron, and A. B. Lemmey The relationship between estimated glomerular filtration rate, demographic and anthropometric variables is mediated by muscle mass in non-diabetic patients with chronic kidney disease Nephrol. Dial. Transplant., December 1, 2006; 21(12): 3488 - 3494. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. H. Macdonald, S. M. Marcora, M. Jibani, G. Roberts, M. J. Kumwenda, R. Glover, J. Barron, and A. B. Lemmey Bioelectrical impedance can be used to predict muscle mass and hence improve estimation of glomerular filtration rate in non-diabetic patients with chronic kidney disease Nephrol. Dial. Transplant., December 1, 2006; 21(12): 3481 - 3487. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
J. Kim, W. Shen, D. Gallagher, A. Jones Jr, Z. Wang, J. Wang, S. Heshka, and S. B Heymsfield Total-body skeletal muscle mass: estimation by dual-energy X-ray absorptiometry in children and adolescents. Am. J. Clinical Nutrition, November 1, 2006; 84(5): 1014 - 1020. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Marcora, F. Casanova, E. Williams, J. Jones, R. Elamanchi, and A. Lemmey Preliminary evidence for cachexia in patients with well-established ankylosing spondylitis Rheumatology, November 1, 2006; 45(11): 1385 - 1388. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 O. A. Kensara, S. A. Wooton, D. I. W. Phillips, M. Patel, D. J. Hoffman, A. A. Jackson, M. Elia, and the Hertfordshire Study Group Substrate-energy metabolism and metabolic risk factors for cardiovascular disease in relation to fetal growth and adult body composition Am J Physiol Endocrinol Metab, August 1, 2006; 291(2): E365 - E371. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 L. J. Woodhouse, A. Mukherjee, S. M. Shalet, and S. Ezzat The Influence of Growth Hormone Status on Physical Impairments, Functional Limitations, and Health-Related Quality of Life in Adults Endocr. Rev., May 1, 2006; 27(3): 287 - 317. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C.-K. Kong and H.-S. S. Wong Weight-for-Height Values and Limb Anthropometric Composition of Tube-Fed Children With Quadriplegic Cerebral Palsy Pediatrics, December 1, 2005; 116(6): e839 - e845. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
O. A Kensara, S. A Wootton, D. I Phillips, M. Patel, A. A Jackson, M. Elia, and Hertfordshire Study Group Fetal programming of body composition: relation between birth weight and body composition measured with dual-energy X-ray absorptiometry and anthropometric methods in older Englishmen Am. J. Clinical Nutrition, November 1, 2005; 82(5): 980 - 987. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
H. H. Choi, P. B. Gray, T. W. Storer, O. M. Calof, L. Woodhouse, A. B. Singh, C. Padero, R. P. Mac, I. Sinha-Hikim, R. Shen, et al. Effects of Testosterone Replacement in Human Immunodeficiency Virus-Infected Women with Weight Loss J. Clin. Endocrinol. Metab., March 1, 2005; 90(3): 1531 - 1541. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
S. Bhasin, L. Woodhouse, R. Casaburi, A. B. Singh, R. P. Mac, M. Lee, K. E. Yarasheski, I. Sinha-Hikim, C. Dzekov, J. Dzekov, et al. Older Men Are as Responsive as Young Men to the Anabolic Effects of Graded Doses of Testosterone on the Skeletal Muscle J. Clin. Endocrinol. Metab., February 1, 2005; 90(2): 678 - 688. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
P. Szulc, F. Duboeuf, F. Marchand, and P. D Delmas Hormonal and lifestyle determinants of appendicular skeletal muscle mass in men: the MINOS study Am. J. Clinical Nutrition, August 1, 2004; 80(2): 496 - 503. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 J. Kim, S. Heshka, D. Gallagher, D. P. Kotler, L. Mayer, J. Albu, W. Shen, P. U. Freda, and S. B. Heymsfield Intermuscular adipose tissue-free skeletal muscle mass: estimation by dual-energy X-ray absorptiometry in adults J Appl Physiol, August 1, 2004; 97(2): 655 - 660. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Jones Jr, W. Shen, M.-P. St-Onge, D. Gallagher, S. Heshka, Z. Wang, and S. B Heymsfield Body-composition differences between African American and white women: relation to resting energy requirements Am. J. Clinical Nutrition, May 1, 2004; 79(5): 780 - 786. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M.-Y. Song, E. Ruts, J. Kim, I. Janumala, S. Heymsfield, and D. Gallagher Sarcopenia and increased adipose tissue infiltration of muscle in elderly African American women Am. J. Clinical Nutrition, May 1, 2004; 79(5): 874 - 880. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 I. Janssen, R. N. Baumgartner, R. Ross, I. H. Rosenberg, and R. Roubenoff Skeletal Muscle Cutpoints Associated with Elevated Physical Disability Risk in Older Men and Women Am. J. Epidemiol., February 15, 2004; 159(4): 413 - 421. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
A. Bosy-Westphal, C. Eichhorn, D. Kutzner, K. Illner, M. Heller, and M. J. Muller The Age-Related Decline in Resting Energy Expenditure in Humans Is Due to the Loss of Fat-Free Mass and to Alterations in Its Metabolically Active Components J. Nutr., July 1, 2003; 133(7): 2356 - 2362. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
Z. Wang, S. Zhu, J. Wang, R. N Pierson Jr, and S. B Heymsfield Whole-body skeletal muscle mass: development and validation of total-body potassium prediction models Am. J. Clinical Nutrition, January 1, 2003; 77(1): 76 - 82. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
) in the model-development group. Total-body SM mass = (1.19 x ALST) - 1.01. R2 = 0.96, P < 0.001, SEE = 1.63 kg. n = 321.