TY - JOUR
T1 - Body composition correlates with laboratory parameters and disease severity in infants with biliary atresia
AU - Marderfeld, Luba
AU - Waisbourd-Zinman, Orith
AU - Biran, Neta
AU - Rozenfeld Bar-Lev, Michal
AU - Poraz, Irit
AU - Reznik, Dana
AU - Jack, Yifat
AU - Shamir, Raanan
N1 - Publisher Copyright: © 2021 Wiley Periodicals LLC.
PY - 2022/5
Y1 - 2022/5
N2 - Aim: Infants with biliary atresia (BA) generally have chronic malnutrition. However, the best anthropometric measure to assess malnutrition and its correlation with disease severity is unknown. We aimed to assess correlations of various anthropometric measurements, including air displacement plethysmography (ADP), with laboratory parameters and with the pediatric end-stage liver disease (PELD) score in infants with BA. Methods: Infants with BA were followed at a pediatric liver transplantation center during 2014–2018. Follow-up comprised laboratory tests and nutritional assessment by a dietitian including dietary intake, weight, height, mid-upper arm circumference (MUAC), and skin-fold thickness. Fat-free mass (FFM) and fat mass (FM) were measured by ADP. Results: Forty-three nutritional evaluations were performed in 28 infants with BA (13 boys, 44.4%). The median age was 20.7 weeks (IQR: 13–25.9). Based on the various anthropometry modalities, infants with BA were found to be malnourished on most of the visits; 63% had a MUAC-Z score lower than −2 standard deviations. High serum bilirubin level predicted lower weight for age, length for age, and MUAC-Z. Lower MUAC-Z was associated with a higher PELD score. Neither FM mass nor FFM correlated with PELD or with serum bilirubin level. However, FM correlated with skin-fold thickness-Z and was low in most patients. Conclusions: The majority of BA infants suffer from malnutrition as assessed by most anthropometrics modalities; low MUAC correlated best with disease severity and serum bilirubin level. Further studies are warranted to determine the contribution of FM measurement by ADP to the anthropometric assessment of infants with BA.
AB - Aim: Infants with biliary atresia (BA) generally have chronic malnutrition. However, the best anthropometric measure to assess malnutrition and its correlation with disease severity is unknown. We aimed to assess correlations of various anthropometric measurements, including air displacement plethysmography (ADP), with laboratory parameters and with the pediatric end-stage liver disease (PELD) score in infants with BA. Methods: Infants with BA were followed at a pediatric liver transplantation center during 2014–2018. Follow-up comprised laboratory tests and nutritional assessment by a dietitian including dietary intake, weight, height, mid-upper arm circumference (MUAC), and skin-fold thickness. Fat-free mass (FFM) and fat mass (FM) were measured by ADP. Results: Forty-three nutritional evaluations were performed in 28 infants with BA (13 boys, 44.4%). The median age was 20.7 weeks (IQR: 13–25.9). Based on the various anthropometry modalities, infants with BA were found to be malnourished on most of the visits; 63% had a MUAC-Z score lower than −2 standard deviations. High serum bilirubin level predicted lower weight for age, length for age, and MUAC-Z. Lower MUAC-Z was associated with a higher PELD score. Neither FM mass nor FFM correlated with PELD or with serum bilirubin level. However, FM correlated with skin-fold thickness-Z and was low in most patients. Conclusions: The majority of BA infants suffer from malnutrition as assessed by most anthropometrics modalities; low MUAC correlated best with disease severity and serum bilirubin level. Further studies are warranted to determine the contribution of FM measurement by ADP to the anthropometric assessment of infants with BA.
KW - Pediatric End-Stage Liver Disease (PELD) score
KW - malnutrition
KW - nutritional assessment
UR - http://www.scopus.com/inward/record.url?scp=85121433529&partnerID=8YFLogxK
U2 - 10.1111/petr.14208
DO - 10.1111/petr.14208
M3 - مقالة
C2 - 34927330
SN - 1397-3142
VL - 26
JO - Pediatric Transplantation
JF - Pediatric Transplantation
IS - 3
M1 - e14208
ER -