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REGULAR ARTICLE
Body composition in late preterm infants in the first 10 days of life and at
full term
Elisabeth Olhager (elisabeth.olhager@skane.se), Caroline T€ornqvist
€ping, Sweden
Division of Paediatrics, Department of Clinical and Experimental Medicine, Faculty of Health Science, Linkoping University, Linko
Keywords ABSTRACT
Air displacement plethysmography, Body Aim: To investigate changes in body weight, fat-free mass, fat mass and percentage of
composition, Fat mass, Fat-free mass, Preterm
infants body fat during early life and at full-term postconceptional age (PCA) in preterm infants
born after 32 gestational weeks and before 37.
Correspondence
E Olhager, Department of Neonatology, Skane Methods: Twenty-nine late preterm infants underwent growth and body composition
University Hospital, SE-221 85 Lund, Sweden. assessment by air displacement plethysmography (ADP) at the age of 4 days and at full-
Tel: +46 46 178286 |
term PCA. In 25 of these infants, body composition was assessed three times between
Email: elisabeth.olhager@skane.se
days four and nine of life. The preterm infants were compared with 29 full-term infants,
Received
matched for gestational age, sex and body weight.
29 September 2013; revised 1 February 2014;
accepted 10 March 2014. Results: There was a significant increase in birth weight and fat-free mass between days
DOI:10.1111/apa.12632
four and nine of life. Preterm infants had significantly more body fat 382 180 g vs
287 160 g than full-term infants at full-term PCA. Preterm infants showed poor linear
growth between birth and full-term PCA.
Conclusion: Weight gain after the initial postnatal weight loss consists of gain in fat-free
mass. At full-term PCA, preterm infants were stunted. When compared with full-term new
born infants matched for body weight and gestational age, preterm infants had more body
fat and a higher percentage of body fat.
©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743 737
Body composition in late preterm infants €rnqvist
Olhager and To
preterm infants, assessed by dual-energy X-ray absorptiom- University Hospital. Gestational age was based on the date
etry (DEXA), was as high as 13–14% (13). of the last menstrual period and ultrasound in gestational
In 2004, equipment based on the air displacement week 11–12. Postconceptional age was calculated using
plethysmography (ADP) technique became available, chronological age plus gestational age. Forty-one of these
enabling accurate, quick and noninvasive assessment of infants met the following criteria: birth weight over 1500
body composition in infants weighing between one and grams, singletons, weight and length appropriate for gesta-
eight kilograms (9,14,15). This technique has subsequently tional age according to Swedish growth reference values
been used to measure the body composition of full-term and (16), no need for respiratory support (ventilator, continued
preterm infants. It is well accepted by parents, healthcare airway pressure or extra oxygen), no need for parenteral
staff and infants and is therefore well suited for clinical nutrition and no sepsis or malformation. Parents were
studies. We used the ADP technique in a group of late asked for permission for their child to participate in the
preterm infants to study changes in body composition study, and permission was granted for 30 infants (29 infants
during the early postnatal period. Our first aim was to had valid results). These infants were all fed according to
describe changes in body weight, fat mass and fat-free mass current practice at the neonatal unit, which includes special
in such infants during the first 10 days of life. Our second efforts to initiate and maintain maternal lactation. As most
aim was to compare their body composition at full-term preterm infants are unable to suck effectively, breast milk
PCA with corresponding values for full-term new born was initially fed through a nasogastric tube. If the mother
infants matched for PCA, sex and weight. was unable to provide breast milk, the infants were fed
formula (Pepti Junior, Mead Johnsson). On day four of life,
nine infants received formula, 13 received formula plus
MATERIALS AND METHODS their mother’s breast milk, and seven only received their
Study design mother’s breast milk. At full-term PCA, two infants were fed
Body weight, fat-free mass and fat mass were assessed in 29 formula, four were fed formula plus breast milk, and 23 only
preterm infants (Group One). The infants were examined received breast milk. Feeding regimes were not recorded
on day four one of life, on two additional occasions between discharge from the unit and the day of assessment.
during the first 10 days of life and at full-term PCA. Four
infants were not assessed on the following two occasions. Full-term infants
Values obtained at full-term PCA were compared with Twenty-nine healthy full-term newborn infants were
those for 29 full-term newborn infants (Group Two). For recruited from the maternity ward at Linko € ping University
this comparison, infants were matched for sex, body weight Hospital. Fourteen had participated in a previous study
(100 g) and PCA (3 days). Infants in Group Two were (17). The infants were fed according to the guidelines of the
examined on day six two of life. Figure 1 shows the maternity unit, where all mothers are encouraged to
infants who participated in the study. breastfeed. At the time of investigation, two infants were
formula fed, two received formula plus breast milk and 25
Preterm infants were completely breastfed.
Between February 2008 and June 2009, 166 preterm
infants, born after at least 32 gestational weeks, were Anthropometry at birth
€ ping
admitted to the neonatal intensive care unit at Linko In the delivery room, all infants were weighed without
clothing on an electronic baby scale (Tanita Corporation,
Tokyo, Japan) and their length measured by means of a
measuring board. Head circumference was measured with a
Group 1
plastic measuring band.
n = 29 preterm infants,
investigated on day four
of life Body composition
Body composition was assessed using an ADP system (Pea
Pod, Cosmed USA Inc., Concord, CA, USA) using software
Four preterm infants were version 3.0.1. The physical design, validation and measure-
not eligable for
investigations on ment procedure have been described in detail elsewhere
day 6 and 9 of life. (15,16). The system measures body volume and body weight
and calculates body density. Body composition is then
calculated by means of a two-compartment model, assum-
Group 1 ing a fat mass density of 0.9007 g/mL and using fat-free
n = 29 preterm infants Group 2 mass density values based on data published by Fomon
investigated att full-term n = 29 full-term infants et al. (18). The validity of Fomon et al.0 s estimates of fat-free
post conceptional age
mass density in full-term newborns has recently been
confirmed (19). Values for preterm infants are based on
Figure 1 Flow diagram of the infants who participated in the study. back-extrapolation using existing reference values for foe-
tuses of different gestational ages (20,21). A recent study has
738 ©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743
€rnqvist
Olhager and To Body composition in late preterm infants
Ethical considerations infants were not examined on days six and nine. Between
The Regional Human Research Ethics Committee in birth and the first examination, the infants lost 4.4 2.5%
Linko€ ping approved the study. Both parents of all infants of their body weight. At the third examination, they had
gave informed oral consent. regained their birth weight. Between the first and third
examinations, there was a significant increase (p < 0.05) in
Statistics body weight, from 2323 363 to 2392 354 grams, and
Data were analysed using the statistical software SPSS for in fat-free mass, from 2176 297 to 2237 275 grams.
Windows, version 18.0 (Chicago, IL, USA). Values are The average increase in body weight was 69 57 grams,
expressed as means (SD). Repeated ANOVA, post hoc and the average increase in fat-free mass was 62 53
Tukey’s test and multiple regressions were used to identify grams. During this period, the average change in body
significant differences between groups. Means were also fat was 0.1 1.2% and the average increase in body
compared using paired and unpaired t-tests. Significance fat 7.0 6.3 grams. This increase in fat mass was not
was accepted when p < 0.05. significant.
©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743 739
Body composition in late preterm infants €rnqvist
Olhager and To
Table 2 Body weight, fat mass and fat-free mass in 29 late preterm infants (four infants did not participate in examinations 2 and 3) assessed three times in the first 10 days of life
Examination Age (days) Body weight (g) Fat mass (%) Fat mass (g) Fat-free mass (g)
† †
1 4 (1) 2323 (363)* 4.9 (3.8) 150 (110) 2176 (297)*
2 6 (1) 2348 (356)* 4.4 (3.8)† 135 (110)† 2216 (293)*
3 9 (2) 2392 (354)* 4.9 (3.3)† 159 (111)† 2237 (275)*
Table 3 Body weight, length, fat mass, fat-free mass, fat mass index and fat-free mass index in 29 late preterm infants (Group One) at first measurement and at full-term PCA
First measurement Full-term PCA p-Value* 95% CI
The z-scores for weight and length at full-term PCA were DISCUSSION
0.62 0.75 and 0.78 0.91, respectively. These values In our study of late preterm infants, we found that the
were significantly lower than the corresponding values at increase in body weight between days four and nine of life
birth, when the weight-for-age z-score was 0.26 0.72, was mainly due to an increase in fat-free mass. Between the
and the length-for-age z-score was 0.1 0.9. There was a fourth day of life and full-term PCA, these infants increased
significant difference between the z-score at PCA and the their fat mass from 153 to 384 grams, equivalent to a fat
z-scores at birth. accretion of 4.2 g/kg/day. The corresponding figure for the
reference foetus is 2–3 g/kg/day during gestational weeks
Body composition of late premature infants compared 33–36 (20). During this period, the weight-for-age and
with full-term infants at similar PCA length-for-age z-scores of the late preterm infants
Table 4 shows the PCA and postnatal age at measurement decreased. Furthermore, at full-term PCA, these infants
together with body weight, length, fat mass, fat-free mass, had significantly less fat-free mass than full-term newborn
fat-free mass index and fat mass index for late preterm infants matched for weight, sex and age.
infants (Group One) and full-term (Group Two) infants Using ADP, this study assessed body composition
measured at comparable PCA. By design, the two groups changes in late preterm infants during the first 10 postnatal
had similar body weights, but the preterm infants were days. A previous study assessed body composition in late
significantly shorter, on average by 2 cm. They also had preterm infants on day five but did not include further
significantly less fat-free mass than the full-term infants, measurements during the first 10 days (8). However, mean
2631 309 versus 2794 329 grams. Furthermore, the body fat as a percentage of body weight was 5.7% in that
preterm infants had significantly more body fat (grams and study, agreeing with our results. Furthermore, body fat as a
percentage) than the full-term infants: 382 180 versus percentage of body weight of our preterm infants on day
287 160 grams, and 12.3 4.9 versus 8.1 4.3%. four of life was consistent with reference data from the
Although the average body weight of the two groups was study of Ziegler et al.(20) who showed that body fat in
very similar, preterm infants had 25.3% more body fat. They foetuses of corresponding gestational ages varies between
also had a significantly lower fat-free mass index (p < 0.05) 6.3 and 8.7%. The higher percentage of body fat in late
but a significantly (p < 0.003) higher fat mass index than preterm infants reported by Lapillone et al. can be
the full-term infants. In both groups, the majority of infants explained by the use of DEXA – a technique that has been
were breastfed. shown to overestimate fat mass in small infants (13,23).
740 ©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743
€rnqvist
Olhager and To Body composition in late preterm infants
Table 4 Body weight, body length, postconceptional age and postnatal age at measurement, fat mass, fat-free mass, percentage of body fat, fat mass index and fat-free mass index
in 29 preterm infants at full-term postconceptional age (Group One) and 29 full-term infants (Group Two)
Preterm infants Full-term infants p-Value* 95% Confidence interval
ADP, by contrast, has been shown to be a valid method (9). at birth but, as Figure 2 shows, they were shorter than both
Thus, we believe that our results are likely more accurate small full-term and normal-sized full-term infants at full-
than those reported by Lapillone et al. At full-term PCA, term PCA, suggesting that their gain in length was restricted
our preterm infants had weighed less, were shorter and had during the first 3 or 4 weeks of extra uterine life. Further-
a lower percentage of body fat than preterm infants assessed more, their proportion of fat-free mass at full-term PCA was
by ADP at full-term PCA (5,8). The infants in the study by less than that of small full-term infants and, of course, of
Ramel et al. contained 18.7 0.8% body fat at full-term normal-sized full-term infants, indicating that the growth of
PCA and the corresponding figure in the study by Roggero this body component, too, was restricted during this period.
et al. was 16.1 4.6%, which are higher values than for our However, preterm and normal-sized full-term infants had
preterm group at full-term PCA (5,8). The reasons for the similar amounts of fat, both in grams and as a percentage.
difference could be that Ramel et al.0 s study included varied This comparison thus emphasizes that the problem for a
samples of preterm infants who were older, between 40 and premature newborn is to gain sufficient fat-free mass and
42 weeks gestational age, when assessed by ADP at full- length. Consequently, future efforts in this area should
term PCA. The differences in the percentage of body fat may attempt to specifically improve these aspects of growth.
reflect variations in international and inter-hospital nutri- An obvious way of improving the growth in fat-free mass
tional regimes. This also means that further studies of and length of premature infants is to manipulate their
changes in body composition in late preterm infants under nutritional intake. Our late preterm infants did not follow a
different nutritional regimes are necessary. In our study, 23 prescribed nutritional schedule and the policy of our unit is
of the preterm infants and 25 of the full-term infants were that all infants should be breastfed at discharge, as breast
breastfed at full-term PCA. The results in this study were not milk is regarded as the optimal food for all preterm infants.
adjusted for feeding regimes. Detailed feeding regimes However, it has been shown that protein-fortified feeds can
between discharge and assessments were not recorded in increase gains in fat-free mass (25). It remains unclear
the preterm group. We believe that confirmation studies whether this can completely correct the kind of diminished
using larger samples sizes and, if possible, randomization to fat-free mass at full-term PCA found in our late preterm
different feeding regimes is required. Furthermore, the full- infants. Further studies of late preterm infants are therefore
term infants were assessed during the first week of life and necessary to examine the effect of such protein supplements
details of feeding were not recorded. Details of feeding were on growth in length and fat-free mass.
not recorded, and thus, it would not be correct to draw any Growth patterns in early life predict subsequent disease
conclusion on how body composition was affected by risks, such as type 2 diabetes and decreased insulin
different feeding regimes. At the time of assessment, most of sensitivity. Intrauterine growth restriction is a risk factor
the infants had not reached their full capacity of feeding. for such diseases, but rapid postnatal weight gain is also
Normal postnatal development in full-term infants independently associated with an increased risk of devel-
involves a rapid increase in total body fat after birth, and oping metabolic syndrome (3,4). These aspects of the
data reported by others tend to suggest that this is also the relationship between early growth and later disease risk
case for infants born prematurely (6,7,12). In Figure 2, we have been discussed by Wells, who introduced the concepts
present a compilation of data with additional information of metabolic load and metabolic capacity (3). A high body
on this issue. The figure presents the results of the present fat content may represent a metabolic load and metabolic
study for our small full-term and preterm infants in relation capacity. Metabolic capacity is defined as organ develop-
to body composition data for 209 normal-sized full-term ment that occurs early in life and metabolic load as the
healthy Swedish infants studied at an average age of 1 week subsequent growth. Disease risk is predicted to be greatest
(24). The preterm infants were of average weight and length when there is large disparity between metabolic capacity
©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743 741
Body composition in late preterm infants €rnqvist
Olhager and To
3500
12
50
Body fat
Fat free mass
3000
10
40
2500
8
30
2000
6
1500
20
4
1000
10
2
500
0
TN TS P TN TS P TN TS P
Figure 2 Figure 2 shows the body weight (g), fat mass (g), length (cm) and body fat (%) of 209 average-size, full-term Swedish infants at an average of 1 week of age
(term normal = TN) (24), plus the small full-term infants (term small = TS, group III) and late preterm infants of the present study (preterm = PT, group II).
and metabolic load. A high body fat content may represent preterm infants have adapted to extra uterine life (11).
a metabolic load, while a low content of fat-free mass may Calculation of the percentage of body fat is based on
be detrimental in terms of metabolic capacity. A low fat-free measurements of body density, assuming a constant density
mass index in relation to body length squared has been of fat mass and fat-free mass. However, in fat-free mass the
found to be an independent risk factor for premature death amount of water, the so-called hydration factor, is an
in adults (26). At full-term PCA, our late premature infants important determiner of fat-free mass density. The hydra-
had a lower fat-free mass index and a higher fat mass index tion factor is known for full-term newborns but not for
ratio than full-term infants. We do not know if these preterm infants (19). Thus, to increase the validity of ADP
observations are of any significance for future health, but it for preterm infants, studies on the degree of hydration
is without doubt warranted to consider such infants‘ body factor would be recommended.
composition characteristics suboptimal. Several maternal factors, such as smoking, parity, pre-
The infants in our study were younger (4 days 1), when eclampsia, maternal body mass index, diabetes and level of
examined by ADP, than those in the validity study by education, have been shown to affect the outcome of a
Roggero et al. (9). Another study reported invalid results mother’s offspring (29). Placental dysfunction is strongly
when small full-term infants are measured soon after birth associated with preterm birth and growth restriction, and
(27). This could indicate that measurement accuracy soon high maternal body mass index and diabetes are associated
after birth and later differs for small infants. It has, however, with increased growth (30). In our study, maternal factors
been shown that the ADP is robust to minor changes in fat- were not recorded and the presented data were not adjusted
free mass hydration in full-term infants (28). In preterm for maternal factors. As preterm birth is often caused by
infants, adaptation to extra uterine life takes longer com- maternal factors, there is reason to believe that the intrauter-
pared with full-term infants (11). ADP values are affected by ine growth of the preterm infants in our study was affected.
lung volume and fluctuation in hydration. Therefore, our The rapid postnatal growth in fat mass could be an effect of
preterm infants were assessed on day four, when most late intrauterine growth restriction caused by maternal factors.
742 ©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743
€rnqvist
Olhager and To Body composition in late preterm infants
In conclusion, we showed that in late preterm infants the 10. Altman M, Vanpee M, Cnattingius S, Norman M. Neonatal
weight gained after the initial postnatal weight loss mainly morbidity in moderately preterm infants: A Swedish national
consisted of a gain in fat-free mass. At full-term PCA, population-based study. J Pediatrics 2011; 152: 239–44.
11. Micheli J-L, Pfister R, Junod S, Laubscher B, Tolsa J-F, Schutz
however, growth in length and fat-free mass was restricted in
Y. Water, energy and early postnatal growth in preterm infants.
these infants. Accretion of body fat, on the other hand, was Acta Paediatr Suppl 1994; 405: 35–42.
comparable with that of healthy newborn infants of average 12. Griffin IJ, Cooke RJ. Development of whole body adiposity in
size. Furthermore, in relation to their length, preterm infants preterm infants. Early Hum Dev 2012; 88: S19–24.
were fatter. This pattern of growth and body composition is 13. Lapillone A, Braillon P, Claris O, Chatelain PG, Delmas PD,
a concern, as it may be associated with increased risks of Salle BL. Body composition in appropriate and in small for
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ACKNOWLEDGEMENTS 15. Ma GS, Yao M, Liu Y, Lin A, Zou H, Urlando A, et al. Validation
We wish express our thanks to the infants who participated of a new pediatric air displacement plethysmograph for assessing
in this study and the staff at the Neonatal Intensive Care body composition in infants. Am J Clin Nutr 2004; 79: 653–60.
16. Niklasson A, Albertsson-Wikland K. Continuous growth
Unit in Linko € ping. We also wish to thank Mats Fredriksson
reference from 24th week of gestation to 24 months by gender.
for statistical advice. We are further grateful to Professor BMC Pediatr 2008; 8: 8, doi:10.1186/1471-2431-8-8.
Elisabet Forsum, Britt Eriksson and Pontus Henriksson for 17. Eriksson B, Lo € f M, Forsum E. Body composition in full-term
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18. Fomon SJ, Haschke F, Ziegler E, Nelson SE. Body composition
of reference children from birth to age 10 years. Am J Clin Nutr
COMPETING INTERESTS
1982; 35: 1169–75.
The authors do not have any conflicts of interest. 19. Eriksson B, Lo € f M, Eriksson O, Hannestad U, Forsum E. Fat-free
mass hydration in newborns: assessment and implications for
body composition studies. Acta Paediatr 2011; 100: 680–6.
ROLE OF FUNDING SOURCE 20. Ziegler E, O0 Donnell A, Nelson S, Fomon S. Body composition
€
The project was funded by Ostergo€ tland County Council of the reference fetus. Growth 1976, 40; 329–41.
and the Samariten Foundation. 21. Dickerson J. Contribution of major soft tissue to total amounts
of body constituents during growth: In Morgan JB, Dickerson
JW, editors. Nutrition in early life. 1 ed. West Sussex, England:
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©2014 Foundation Acta Pædiatrica. Published by John Wiley & Sons Ltd 2014 103, pp. 737–743 743