JACN
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Koo, B.
Right arrow Articles by Koo, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koo, B.
Right arrow Articles by Koo, W.
Journal of the American College of Nutrition, Vol. 21, No. 3, 245-249 (2002)
Published by the American College of Nutrition


Original Research

Body Composition of Newborn Twins: Intrapair Differences

Belinda Koo, MA, Jocelyn Walters, MS, Elaine Hockman, PhD and Winston Koo, MBBS,

Departments of Pediatrics, Obstetrics and Gynecology, University of Tennessee, Memphis, Tennessee (B.K., J.W., W.K.)
Department of Pediatrics, Hutzel Hospital (W.K.), Detroit, Michigan
Computing and Information Technology, Wayne State University (E.H.), Detroit, Michigan

Address correspondence to: Dr. Winston Koo, Department of Pediatrics, Hutzel Hospital, 4707 St Antoine Blvd, Detroit, MI 48201. E-mail: wkoo{at}wayne.edu


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Objective: To measure body composition in newborn twins and to test the hypothesis that differences in body weights between twins are reflected proportionally by their differences in various components of body composition.

Methods: 48 pairs of newborn twins delivered at a tertiary teaching hospital had dual energy x-ray absorptiometry (DXA) body composition measurement for bone mineral content (BMC), lean and fat mass (LM, FM). Data analyzed with regression and analysis of variance.

Results: Body weight, BMC, LM and FM increased with increased gestational age (p < 0.001). The percent difference in BW between each twin pair was significantly correlated with percent difference in BMC, LM, and FM (p < 0.001). However, mean (± SD) percent difference in body weight (14.3 ± 10.0%) was significantly lower (p < 0.001) than FM (26.0 ± 15.0%) but was not significantly different from LM (13.4 ± 9.0%) or BMC (15.9 ± 11.6%).

Conclusion: In newborn twins, body weight and body composition varies with gestational age. For any twin pair, a difference in body weight was correlated with but not proportional to differences in individual components of body composition.

Key words: body composition, neonates, twins, growth, bone, lean tissue, fat


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Discrepant fetal growth in twin pregnancy is well known. It has been defined as the difference in birth weight between twins of greater than 15% [1], 20% [2], 30% [3] or more [4,5]. Its presence is associated with increased risk of perinatal morbidity and mortality [36] and long-term physical and intellectual impairment [4]. However, other than standard anthropometric and fetal ultrasound measurements [2,7], there has been no systematic study on the relative contribution of different components of body composition to the body weight of twins.

Information on body composition of twins may contribute to the knowledge on physiological changes during normal and abnormal fetal growth. It also may lead to better postnatal nutritional management of the growth impaired twin if the goal is to achieve body composition similar to the normally grown twin. This study aims to determine the variations in anthropometric and body composition measurements of newborn twins at different gestational ages and to test the hypothesis that differences in body weights between twins are reflected proportionally by differences in various components of body composition, specifically lean body mass, fat mass and bone mineral content.


    SUBJECTS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Subjects
Subjects included 48 pairs of twins with birth weights from 976 g to 3135 g and gestation ages from 30 to 40 weeks. Gestational age assessment was based on menstrual and/or ultrasound dating and confirmed by standard physical examination [8]. Seven pairs of twins were <33 weeks gestational age, 29 pairs were between 33 and 36 weeks, and 12 pairs were >=37 weeks. In 29 pairs, both twins had birth weights appropriate for gestational age (AGA, between 10th to 90th percentiles) [9]; in one pair, both twins were small for gestational age (SGA, less than 10th percentile); and in 18 pairs, one twin was AGA while the other twin was SGA. There were 23 pairs of twins with a difference in birth weight of greater than 15%. Thirty-seven pairs of twins were African American (38 males and 36 females; 21 pairs were of the same gender), 10 pairs were Caucasian (14 males and 6 females; 8 pairs were of the same gender), and one pair was Asian (1 male and 1 female).

Clinical care of all study subjects was managed by the attending physician, and all infants were clinically well at the time of study. There was no congenital malformation or specific conditions other than that related to multiple fetuses to account for the growth discrepancy within each twin pair. This study was approved by the Institutional Review Board for human subjects at the University of Tennessee-Memphis, and written informed consent was obtained from each subject’s parent.

Anthropometric Measurements
Nude weight, length and head circumference of each infant was measured immediately preceding dual energy x-ray absorptiometry (DXA) study. Weight in grams was determined with a digital electronic scale (Air Shields Vickers, Hatboro, PA). The scale was regularly maintained by the hospital Biomedical Instrumentation personnel and calibrated with known standard weights. Recumbent length was the average of two consecutive measurements within 0.4 cm and was determined using a standard length board (Ellard Instrumentation Ltd., Seattle, WA). Head circumference was the average of two consecutive maximum occipitofrontal circumferences within 0.2 cm using a disposable paper tape measure.

DXA measurements
DXA whole body scans were performed at a mean of 3.8 ± 3.2 (SD) days after birth using a pencil beam densitometer (Hologic QDR 1000/W. Hologic Inc., Waltham, MA). Forty-two pairs of twins were studied on the same day. Six pairs of twins were studied at one to four days apart while awaiting recovery from minor illnesses in one of the twins.

Details of DXA measurements have been reported [10,11]. Briefly, all scans were performed with the subject and a step phantom placed on top of an infant platform with an interposing cotton blanket. Each subject was swaddled in another cotton blanket during scanning. All infants were scanned without sedation or additional restraint. Each scan was judged technically satisfactory if the external calibration step phantom and the skeletal outline of the subject laid within the scan region as shown on the video monitor and if there was no significant movement artifact [11]. Scan analysis was performed using the software developed in conjunction with the manufacturer (Version V5.64P).

Quality control scans were performed daily on a manufacturer-supplied anthropomorphic spine phantom, and the long term (>3 years) coefficients of variation for the determination of bone mineral content, bone area and bone mineral density on repeated measurements of spine phantom were <0.3% for all parameters. The average annual rate of change for each of these measurements was not significantly different from zero. In our laboratory, the in vivo replication of DXA measurements in 50 infants (17 infants were neonates with weights between 1525g and 5128g) was highly significantly correlated (r >= 0.99 and p < 0.001 for all parameters, i.e., bone mineral content, bone area, bone mineral density, lean body mass and total fat mass), and the standard deviation of difference [12] between paired DXA measurements for the same parameters was 3.8%, 2.5%, 2.6%, 2.3% and 7.0%, respectively.

Statistical Analyses
The difference in weight, length and each measured DXA variable (lean body mass, fat mass, bone mineral content, bone area) between each twin pair was expressed as a percentage of the larger twin with the formula [(larger infant-smaller infant)/(larger infant)] x 100. Bone mineral density was used only as descriptive data and was not analyzed statistically because it is based on bone mineral content divided by area and there are a number of concerns with its use in pediatrics [13].

Regression analysis was used to determine 1) whether the percent difference in birth weights or body composition components listed above was related to gestational age and 2) the change in anthropometric and DXA measurements with increased gestational age for individual infants. Pearson correlation was used to determine the relationship among percent differences in nude weight, lean body mass, fat mass and bone mineral content.

Repeated measure analysis of variance was used to test the premise that the percent difference in nude weight between twins would be equal to the percent difference of each weight component of body composition, namely lean body mass, fat mass and bone mineral content. The dependent variables were percent difference between each twin pair in nude weight, lean body mass, fat mass and bone mineral content, i.e., the four percent differences would be statistically equivalent based on testing our hypothesis with repeated measures analysis of variance. The analysis was controlled for race (African American vs. non-African American) and gender (same sex vs. different sex). Repeated measures analysis of variance was then repeated with each within-subject factor adjusted for DXA measured area. Orthogonal contrasts using Difference and Helmert methods were used to test for differences among nude weight and body composition variables.

To further explore the relation of gender to differences in weight and body composition, the gender variable was further divided into four categories for each twin pair (i.e., both males, both females, male weighing more than female, female weighing more than male), and the same statistical procedure was repeated. In addition, the Bonferroni test was used for post hoc comparison among the four categories of the gender variable. Power was computed for the analyses completed. All statistical tests were performed with SPSS 10.0 (SPSS Inc., Chicago, IL) for windows at an adopted significance level of p < 0.05.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
There was no significant relation between the magnitudes of intrapair difference in body weight or body composition (lean body mass, fat mass, bone mineral content, bone area) with the gestational age (adjusted r2 <= 0.02 for all comparisons). Anthropometric and DXA measurements of individual subjects were significantly (p < 0.001 for all comparisons) higher with increased gestational age (Figs. 1 and 2). With increasing gestational ages, there was an increase in bone mineral content and fat mass, but a decrease in lean body mass as a percentage of the body weight.



View larger version (17K):
[in this window]
[in a new window]
 
Fig. 1. Scatter plot including mean regression line for anthropometric measurements of all study infants (n = 96) as a function of gestational age (GA) in weeks. Nude weight g = -2736 + 137.97 GA, r = 0.75, p < 0.001. Length cm = 21.7 + 0.63 GA, r = 0.65, p < 0.001. Head circumference (HC) cm = 12.3 + 0.55 GA, r = 0.64, p < 0.001.

 


View larger version (14K):
[in this window]
[in a new window]
 
Fig. 2. Scatter plot including mean regression line for body composition measurements of all study infants (n = 96) as a function of gestational age (GA) in weeks. Lean body mass g = -2179 + 116.49 GA, r = 0.76, p < 0.001. Fat mass g = -574 + 23.27 GA, r = 0.56, p < 0.001. Bone mineral content (BMC) g = -70.3 + 3.09 GA, r = 0.72, p < 0.001.

 
The intrapair percent difference in nude weight was significantly (p < 0.001 for all comparisons) correlated with percent difference in each of the body composition components: lean body mass (r = 0.93), bone mineral content (r = 0.75) and fat mass (r = 0.55). However, the percent difference in fat mass was significantly higher than the percent difference in nude weight, lean body mass and bone mineral content (Table 1).


View this table:
[in this window]
[in a new window]
 
Table 1. Percent Difference* in Anthropometric and Dual Energy X-Ray Absorptiometry (DXA) Measurements for the 48 Pairs of Twins

 
There was a tendency for an interaction between percent difference in body composition and race (p = 0.056, repeated measures analysis of variance) with African American twins having a lower percent difference in lean body mass (p < 0.05, repeated measures analysis of variance with contrast). However, the racial effect was no longer present after adjusting each dependent variable by DXA bone area.

There was no gender effect, whether it was categorized as same or different gender pairs, or in the four combinations of gender pairing as described above. In addition, no interaction effect among the dependent variables with race or gender was present in any analyses.

From a prospective aspect with the assumption that, for any twin pregnancy, the larger and presumably normally grown twin has similar body composition to that of a singleton [14,15] and the smaller twin would have discrepant body composition, then a sample size of 40 pairs of twins is expected to detect a minimum of 15% difference in at least one of the body composition components with an {alpha} of 0.05 and a power of 0.71, whereas 50 pairs would increase the power to 0.80. Post hoc calculation shows that the observed power was >0.90 for all analyses.


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
This study employed the DXA technique because of its ability to simultaneously measure multiple components of body composition and the increasing availability of normal data during infancy [16]. Validation studies for the current version of software have been performed on piglets as small as 886g [10,17,18], and it is generally agreed that DXA measurements better reflect the chemical determination of lean and bone masses compared to fat mass [17,18]. However, the stability and precision of each DXA parameter of body composition measurements in our laboratory indicate that our data provided accurate discriminative power for differences in body composition between subjects; that is, clinically relevant parameters of body composition for the management of growth retarded twins can be determined using this technique.

To our knowledge, this is the first report on the relative contribution of several components of body composition involving soft tissues (fat and lean body mass) and bone in twins. For all infants, the pattern of changes in anthropometric and body composition measurements with increased gestational age are consistent with that reported for normal singleton infants [14,15], specifically, an increase in absolute values for all measurements, but a small decrease in lean body mass as a percentage of total weight.

We used differences in body weight for comparison with differences in body composition because body weight is an accurate and reproducible measurement and is freely available. In addition, we [14,15,19] and others [20,21] have shown that body weight is a major physiological predictor of body composition during infancy. In this study, the data were analyzed as a continuum to better reflect fetal growth rather than arbitrarily defining discrepant fetal growth based on appropriateness of the birth weight for gestational age of each infant or a 15% to 30% difference in body weight. The use of arbitrary grouping may have some value for the prediction of clinical course, but it lacks specificity for use in individual infants. It also ignores errors of measurement with loss of data and loss of power particularly around the cut-off point [22]. The magnitude of differences in body weight and body composition variables (lean body mass, fat mass, bone mineral content and bone area) were not related to gestational age; thus further analysis based on stratification by gestational age would not be justified.

We controlled for race and gender in our data analyses, since race had a small influence on DXA bone mass measurements based on univariate analyses [14] and females had more fat mass and less lean body mass than males [15]. The racial effect showing lower percent difference in lean body mass compared to the differences in fat mass and bone mineral content was statistically insignificant once we controlled for DXA bone area, suggesting that body size is of greater importance in determining body composition. Our data also demonstrated that gender pairing did not have an effect on body composition among twins. This would support the conclusion that growth and body composition within any twin pair are independent of gender.

The lack of detail data on placental anatomy for our subjects limits the interpretation on the role of placental circulation that might account for the altered growth and body composition. The absence of specific conditions such as congenital malformation that affected only one fetus of a twin pair suggest that any adverse in-utero event that may affect growth and body composition could affect both twins, although the susceptibility to adverse events might differ within and between twin pairs. In any case, our data on the differences in body composition among twin pairs are consistent with the reports in singleton infants that body fat is most frequently affected and to the greatest extent by abnormal fetal growth. This appears to be the case whether the fetal growth was impaired [2325] or was excessive [26]. We have now demonstrated that the deficit in body fat is also greater than the deficit in lean or bone mass in the smaller or growth retarded twin compared to the larger twin. This alteration in body composition appears to be the case in the range of differences in body weights (up to 42%) among the twin pairs studied.

In this study, body weight is disproportionately affected to a greater extent than length or head circumference. This finding supports the presence of asymmetric growth retardation, an indication of nutrient deficiency as the primary cause of growth discrepancy, in contrast to the more uniform decrease in weight, length and head circumference that would be expected from other causes such as chromosome abnormalities or severe intrauterine infection. While a greater intake of energy is usually recommended for growth impaired infants, it is important to note that the difference in body weight is also reflected in differences in lean body mass and bone mineral content. Our findings suggest that an increase in all nutrients with a proportionally greater energy intake is most appropriate for postnatal "catch up" on all components of body composition.


    CONCLUSION
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 
Anthropometric and body composition measurements of twins increased with advancing gestational age. However, difference in body weights between neonates for any twin pair is correlated with but is not proportional to differences in individual components of body composition. Lean body mass and bone mass are relatively better preserved than fat mass in the growth impaired twin, and these changes are independent of race or gender.


    ACKNOWLEDGMENTS
 
Supported by a University of Tennessee Medical Research Grant and by The University of Tennessee—Memphis Clinical Research Center, USPHS Grant RR 00211-29.

Received August 15, 2001. Accepted December 14, 2001.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 SUBJECTS AND METHODS
 RESULTS
 DISCUSSION
 CONCLUSION
 REFERENCES
 

  1. Blickstein I, Shoham-Schwartz Z, Lancet M, Borenstein R: Characterization of the growth-discordant twin. Obstet Gynecol70 :11 –15,1987 .[Medline]
  2. Philip AG: Term twins with discordant birth weights: observations at birth and one year. Acta Genet Med Gemellol30 :203 –212,1981 .[Medline]
  3. Cheung VYT, Bocking AD, Dasilva OP: Preterm discordant twins: what birth weight difference is significant? Am J Obstet Gynecol172 :955 –959,1995 .[Medline]
  4. Blickstein I, Lancet M: The growth discordant twin. Obstet Gynecol Surv43 :509 –515,1988 .[Medline]
  5. Hollier LM, McIntire DD, Leveno KJ: Outcome of twin pregnancies according to intrapair birth weight differences. Obstet Gynecol94 :1006 –1010,1999 .[Medline]
  6. Yalcin HR, Zorlu G, Lembet A, Ozden S, Gokmen O: The significance of birth weight difference in discordant twins: a level to standardize? Acta Obstet Gynecol Scand77 :28 –31,1998 .[Medline]
  7. Kuno A, Akiyama M, Yanagihara T, Hata T: Comparison of fetal growth in singleton, twin, and triplet pregnancies. Human Reprod14 :1352 –1360,1999 .[Abstract/Free Full Text]
  8. Ballard JL, Khoury JC, Wedig K, Wang L, Eilers-Walsman BL, Lipp R: New Ballard score, expanded to include extremely premature infants. J Pediatr119 :417 –423,1991 .[Medline]
  9. Brenner WE, Edelman DA, Hendricks CH: A standard of fetal growth for the United States of America. Am J Obstet Gynecol126 :555 –564,1976 .[Medline]
  10. Koo WWK, Massom LR, Walters J: Validation of accuracy and precision of dual energy x-ray absorptiometry for infants. J Bone Mineral Res10 :1111 –1115,1995 .[Medline]
  11. Koo WWK, Walters J, Bush AJ: Technical considerations of dual energy x-ray absorptiometry based bone mineral measurements for pediatric studies. J Bone Mineral Res10 :1998 –2004,1995 .[Medline]
  12. Bland JM, Altman DG: Statistical methods for assessing agreement between two methods of clinical measurement. Lancet1 :307 –310,1986 .[Medline]
  13. Nelson DA, Koo WWK: Interpretation of absorptiometric bone mass measurements in the growing skeleton: issues and limitations. Calcif Tiss Internat65 :1 –3,1999 .[Medline]
  14. Koo WWK, Walters J, Bush AJ, Chesney RW, Carlson SE: Dual energy x-ray absorptiometry studies of bone mineral status in newborn infants. J Bone Miner Res11 :997 –1002,1996 .[Medline]
  15. Koo WWK, Walters JC, Hockman EM: Body composition in infants at birth and postnatally. J Nutr130 :2188 –2194,2000 .[Abstract/Free Full Text]
  16. Koo WWK: Body composition measurements during infancy. Ann NY Acad Sci904 :383 –392,2000 .[Medline]
  17. Picaud JC, Rigo J, Nyamugabo K, Milet J, Senterre J: Evaluation of dual energy X ray absorptiometry for body composition assessment in piglets and term human neonates. Am J Clin Nutr63 :157 –163,1996 .[Abstract/Free Full Text]
  18. Fusch C, Slotboom J, Fuehrer U, Schumacher R, Keisker A, Zimmermann W, Moessinger A, Boesch C, Blum J: Neonatal body composition: dual energy X ray absorptiometry, magnetic resonance imaging, and three dimensional chemical shift imaging versus chemical analysis in piglets. Pediatr Res46 :465 –473,1999 .[Medline]
  19. Koo WWK, Bush AJ, Walters J, Carlson SE: Postnatal development of bone mineral status during infancy. J Amer Coll Nutr17 :65 –70,1998 .[Abstract/Free Full Text]
  20. Lapillonne A, Braillon P, Claris O, Chatelain PG, Delmas PD, Salle BL: Body composition in appropriate and in small for gestational age infants. Acta Paediatr86 :196 –200,1997 .[Medline]
  21. Rigo J, Nyamugabo K, Picaud JC, Gerard P, Pieltain C, DeCurtis M: Reference values of body composition obtained by dual energy X-ray absorptiometry in preterm and term neonates. J Pediatr Gastroenterol Nutr27 :184 –190,1998 .[Medline]
  22. Cohen J: The cost of dichotomization. Appl Psychol Measurement7 :249 –253,1983 .
  23. Petersen S, Gotfredsen A, Knudsen FU: Lean body mass in small for gestational age and appropriate for gestational age infants. J Pediatr113 :886 –889,1988 .[Medline]
  24. Gartner A, Sarda P, Dupuy RP, Maire B, Delpeuch F, Rieu D: Bioelectrical impedance analysis in small- and appropriate-for-gestational-age newborn infants. Eur J Clin Nutr48 :425 –432,1994 .[Medline]
  25. Drossou V, Diamanti E, Noutsia H, Konstantinides J, Katsougiannopoulos V: Accuracy of anthropometric measurements in predicting symptomatic SGA and LGA neonates. Acta Paediatr84 :1 –5,1995 .[Medline]
  26. Hammami M, Walters JC, Hockman EM, Koo WWK: Disproportionate alterations in body composition of large for gestational age neonates. J Pediatr138 :817 –821,2001 .[Medline]




This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Koo, B.
Right arrow Articles by Koo, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Koo, B.
Right arrow Articles by Koo, W.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS