Premature birth, low birth weight, small for gestational age and chronic non-communicable diseases in adult life: A systematic review with meta-analysis

Early Hum Dev. 2020 Oct:149:105154. doi: 10.1016/j.earlhumdev.2020.105154. Epub 2020 Aug 8.

Abstract

Background: Individuals who were born prematurely (PT), with low birth weight (LBW), or small for gestational age (SGA) appear to present a set of permanent changes that make them more susceptible to develop chronic non-communicable diseases (CNCD) in adult life.

Aim: Investigating the association between PT birth, LBW or SGA at birth and CNCD incidence in adult life.

Methods: Systematic review with meta-analysis of studies available in three databases - two of them are official (PubMed and Web of Science) and one is gray literature (OpenGrey) - based on pre-established search and eligibility criteria.

Results: Sixty-four studies were included in the review, 93.7% of them only investigated one of the exposure variables (46.7% LBW, 35.0% PT and 18.3% SGA at birth), whereas 6.3% investigated more than one exposure variable (50.0% LBW and PT; 50.0% SGA and PT). There was association among all exposure variables in the following outcomes: cardiometabolic (CMD) and glycidic metabolism (GMD) disorders, changes in body composition and risk of developing metabolic syndrome (MS). Female sex was identified as risk factor in the exposure-outcome association. Eighteen (18) articles were included in the meta-analysis. There was positive association between LBW and incidence of CMD (OR: 1.25 [95%CI: 1.11; 1.41]; 07 studies), GMD (OR: 1.70 [95%CI: 1.25; 2.30]; 03 studies) and MS (OR: 1.75 [95%CI: 1.27; 2.40]; 02 studies) in adult life. PT was positively associated with CMD (OR: 1.38 [95%CI: 1.27; 1.51]; 05 studies).

Conclusions: LBW and PT are associated with CMD and GMD development, as well as with the risk of developing MS in adult life.

Keywords: Adult; Low birth weight; Metabolic syndrome; Premature birth.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Adult
  • Cardiometabolic Risk Factors
  • Diabetes Mellitus, Type 2 / epidemiology*
  • Female
  • Humans
  • Hypertension / epidemiology*
  • Infant, Newborn
  • Infant, Premature / growth & development*
  • Infant, Small for Gestational Age / growth & development*
  • Male
  • Metabolic Syndrome / epidemiology*
  • Sex Factors