Differentiating the Preterm Phenotype: Distinct Profiles of Cognitive and Behavioral Development Following Late and Moderately Preterm Birth - 31/01/18
Abstract |
Objectives |
To explore patterns of comorbidity in cognitive and behavioral outcomes at 2 years' corrected age among children born late or moderately preterm (LMPT) and to identify predictors of different patterns of comorbidity.
Study design |
Geographical, prospective population-based cohort study of 1139 infants born LMPT (320/7 to 366/7 weeks' gestation) and 1255 infants born at term (370/7 to 426/7 weeks' gestation). Parent questionnaires were obtained to identify impaired cognitive and language development, behavioral problems, delayed social–emotional competence, autistic features, and clinically significant eating difficulties at 24 months corrected age for 638 (57%) children born LMPT and 765 (62%) children born at term.
Results |
Latent class analysis revealed 2 profiles of development among the term group: optimal (84%) and a profile of social, emotional, and behavioral impairments termed “nonoptimal” (16%). These 2 profiles were also identified among the LMPT group (optimal: 67%; nonoptimal: 26%). In the LMPT group, a third profile was identified (7%) that was similar to the phenotype previously identified in infants born very preterm. Nonwhite ethnicity, socioeconomic risk, and not receiving breast milk at hospital discharge were risk factors for nonoptimal outcomes in both groups. Male sex, greater gestational age, and pre-eclampsia were only associated with the preterm phenotype.
Conclusions |
Among children born LMPT with parent-reported cognitive or behavioral impairments, most had problems similar to the profile of difficulties observed in children born at term. A smaller proportion of children born LMPT had impairments consistent with the “very preterm phenotype” which are likely to have arisen through a preterm pathway. These results suggest that prematurity may affect development through several etiologic pathways in the late and moderately preterm population.
Le texte complet de cet article est disponible en PDF.Keywords : preterm, development, cognition, language, comorbidity
Abbreviations : AIC, BIC, BIC*, BITSEA, CAIC, LCA, LMPT, M-CHAT, SGA, VP
Plan
Funded by the National Institute for Health Research (NIHR) under its Programme Grants for Applied Research (PGfAR) Programme (RP-PG-0407-10029). N.M. receives funding from the Department of Health's NIHR Biomedical Research Centres funding scheme at University College London Hospitals NHS Foundation Trust/University College London. The authors declare no conflicts of interest. |
Vol 193
P. 85 - février 2018 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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