# Neurodevelopmental risks of late-preterm and early-term births: a population-based study from Finland

**Authors:** Samson Nivins, Mika Gissler, Catharina Lavebratt

PMC · DOI: 10.1136/bmjph-2025-003708 · BMJ Public Health · 2026-02-27

## TL;DR

Late-preterm and early-term births are linked to higher risks of neurodevelopmental disorders, even after accounting for shared family factors.

## Contribution

The study provides population-based evidence on neurodevelopmental risks for late-preterm and early-term births, including communication and motor disorders.

## Key findings

- Children born late-preterm had the highest risk of communication, motor, and learning disorders.
- Risks persisted after adjusting for familial and environmental confounders.
- Prevalence of neurodevelopmental disorders decreased with increasing gestational age.

## Abstract

Being born late-preterm and early-term is a known risk factor for neurodevelopmental disorders; however, most studies have focused on intellectual disabilities (ID), autism spectrum disorder (ASD), and attention-deficit/hyperactivity disorder (ADHD), with limited attention to diagnostically distinct disorders of communication or motor development. It remains unclear whether these associations are directly attributed to earlier birth or confounded by shared genetic and environmental factors.

This population-based cohort study included over 1 million singleton children born between 34+0 and 40+6 weeks of gestation in Finland during 1996 and 2014, with follow-up for neurodevelopmental disorders through December 2021. Cox proportional hazards models estimated associations between gestational age at birth and risk for neurodevelopmental disorders, adjusting for confounders. Sibling-pair analyses assessed the influence of unmeasured shared familial factors.

Of the cohort, 2.0% were born at 34+0 to 35+6 weeks, 7.8% at 36+0 to 37+6 weeks, 13% at 38 weeks and 76.5% between 39+0 and 40+6 weeks. Prevalence of neurodevelopmental disorders declined with increasing gestational age: 21.6% at 34+0 to 35+6 weeks, 19% at 36+0 to 37+6 weeks, 16% at 38+0 to 38+6 weeks and 15% at 39+0 to 40+6 weeks (full-term). Compared with full-term, children born between 34+0 and 38+6 weeks had a higher risk of communication disorders, motor disorders and specific learning disorders, with the greatest risks among late-preterm births; risk estimates were similar across sexes. These associations persisted after adjustment for potential confounders, including familial factors shared between siblings. Risks for ID, ASD and ADHD were also observed.

Being born late-preterm and early-term is associated with higher risks of neurodevelopmental disorders. These groups have traditionally received less attention, often being considered at low risk. Our findings underscore the importance of recognising that even late-preterm and early-term births carry measurable neurodevelopmental risk. Promoting longer gestation may support more optimal neurodevelopmental outcomes.

## Linked entities

- **Diseases:** autism spectrum disorder (MONDO:0005258), attention-deficit/hyperactivity disorder (MONDO:0007743), intellectual disabilities (MONDO:0001071)

## Full-text entities

- **Genes:** GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}
- **Diseases:** maternal (MESH:D000079262), Neurodevelopmental disorders (MESH:D002658), motor disorders (MESH:D000068079), cognitive impairment (MESH:D003072), communication disorders (MESH:D003147), neonatal hypoglycaemia (MESH:D007232), ADHD (MESH:D001289), Tourette syndrome (MESH:D005879), infection (MESH:D007239), Gestational hypertension (MESH:D046110), motor and language delays (MESH:D007805), Motor, communication, and specific learning disorders (MESH:D000067559), ID (MESH:D008607), PCOS (MESH:D011085), Chronic hypertension (MESH:D006973), hypoxia (MESH:D000860), type 1, type 2 or gestational (MESH:D016640), smoking (MESH:D015208), respiratory disorders (MESH:D012131), developmental coordination disorder (MESH:D019957), learning disorders (MESH:D007859), diabetes (MESH:D003920), mental and behavioural disorders (MESH:D001523), DM (MESH:D009223), tic disorders (MESH:D013981), Pre-eclampsia (MESH:D011225), cerebral palsy (MESH:D002547), conduct disorders (MESH:D019955), metabolic disturbances (MESH:D024821), reading and (MESH:D004410), neurodevelopmental disturbances (MESH:D014832), ASD (MESH:D000067877)
- **Chemicals:** glucose (MESH:D005947), stimulants (-), insulin (MESH:D007328), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12958876/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12958876/full.md

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Source: https://tomesphere.com/paper/PMC12958876