Divya Keerthy, Angela Holuba, David Bateman, Sudha Kashyap
{"title":"Effects of protein intake on IGF1 and ROP.","authors":"Divya Keerthy, Angela Holuba, David Bateman, Sudha Kashyap","doi":"10.1177/19345798251351004","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundInsulin-like growth factor 1 has been implicated in neural and retinal cell maturation. Optimizing insulin-like growth factor 1 may prevent morbidities, like retinopathy of prematurity. Our objective was to determine the effects of higher protein in parenteral nutrition for very low birth weight infants on insulin-like growth factor 1 and retinopathy of prematurity.MethodsThis was a post-hoc analysis of a prospective, double blind, randomized control trial of appropriate for gestational age, preterm infants (<1250 grams) randomized to high protein (<i>N</i> = 53) or conventional protein (<i>N</i> = 47) in early parenteral nutrition. Goal protein intake was 4 g/kg/d for high protein group and 3 g/kg/d for conventional protein group. Weekly insulin-like growth factor 1 and standard retinal examinations were evaluated.ResultsInsulin-like growth factor 1 was significantly associated with protein intake group controlling for postnatal age, gestational age and sex. Insulin-like growth factor 1 increased by 21.9% (<i>p</i> = 0.03) in the high protein group. Any retinopathy of prematurity or severe retinopathy of prematurity (grade ≥3 and/or plus disease) was not associated with group, actual daily protein intake or insulin-like growth factor 1. However, high protein group was associated with lower risk of plus disease (OR 0.17, <i>p</i> = 0.02). Infants with plus disease had 25% lower mean insulin-like growth factor 1 (<i>p</i> = 0.052).ConclusionHigher protein in parenteral nutrition was associated with increased insulin-like growth factor 1 and lower risk of plus disease in very low birth weight infants.</p>","PeriodicalId":16537,"journal":{"name":"Journal of neonatal-perinatal medicine","volume":" ","pages":"19345798251351004"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of neonatal-perinatal medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/19345798251351004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
BackgroundInsulin-like growth factor 1 has been implicated in neural and retinal cell maturation. Optimizing insulin-like growth factor 1 may prevent morbidities, like retinopathy of prematurity. Our objective was to determine the effects of higher protein in parenteral nutrition for very low birth weight infants on insulin-like growth factor 1 and retinopathy of prematurity.MethodsThis was a post-hoc analysis of a prospective, double blind, randomized control trial of appropriate for gestational age, preterm infants (<1250 grams) randomized to high protein (N = 53) or conventional protein (N = 47) in early parenteral nutrition. Goal protein intake was 4 g/kg/d for high protein group and 3 g/kg/d for conventional protein group. Weekly insulin-like growth factor 1 and standard retinal examinations were evaluated.ResultsInsulin-like growth factor 1 was significantly associated with protein intake group controlling for postnatal age, gestational age and sex. Insulin-like growth factor 1 increased by 21.9% (p = 0.03) in the high protein group. Any retinopathy of prematurity or severe retinopathy of prematurity (grade ≥3 and/or plus disease) was not associated with group, actual daily protein intake or insulin-like growth factor 1. However, high protein group was associated with lower risk of plus disease (OR 0.17, p = 0.02). Infants with plus disease had 25% lower mean insulin-like growth factor 1 (p = 0.052).ConclusionHigher protein in parenteral nutrition was associated with increased insulin-like growth factor 1 and lower risk of plus disease in very low birth weight infants.