# Risk factors and long-term outcomes of infantile colic: A nationwide population-based study

**Authors:** Fang Min Liao, Yin-Ting Chen, Shang-Po Shen, Chau-Ren Jung, An-Chyi Chen, Shu-Fen Wu, Yu-Chia Chang, Hung-Chih Lin

PMC · DOI: 10.1038/s41598-025-34646-4 · Scientific Reports · 2026-01-13

## TL;DR

This study finds that infantile colic is linked to long-term health issues like gut disorders and ADHD, and is associated with factors like C-sections and maternal health conditions.

## Contribution

The study provides new evidence linking infantile colic to long-term gut-brain interaction disorders and neurodevelopmental risks.

## Key findings

- Infantile colic is associated with higher risks of gut-brain interaction disorders like IBS and functional abdominal pain.
- Children with colic had increased risks of ADHD and atopic diseases.
- Risk factors include neonatal antibiotic use, C-section delivery, and maternal atopic or mental health conditions.

## Abstract

Infantile colic is a common condition during early infancy with unclear etiology, likely involving multifactorial mechanisms and gut dysbiosis. This nationwide population-based study investigated perinatal risk factors and long-term health outcomes associated with infantile colic. Using Taiwan’s national birth cohort data from 2010 to 2015, we identified 19,191 infants with colic and 95,955 matched controls. The inclusion criteria for the infantile colic group were having two or more related ICD codes (ICD-9-CM 789.0x and 780.9) between 1 and 5 months of age. Conditional logistic regression was applied to identify associated risk factors, and Cox proportional hazard models assessed outcomes over a 5-year follow-up. Infantile colic was significantly associated with neonatal antibiotic use, cesarean delivery, maternal atopic diseases, maternal major depressive disorder, and maternal irritable bowel syndrome. Children with a history of colic exhibited higher incidence rates of disorders of gut-brain interaction, including constipation, diarrhea, irritable bowel syndrome, and other functional abdominal pain disorders. Additionally, increased risks of attention deficit hyperactivity disorder and atopic diseases were observed. These findings suggest that infantile colic may reflect early-life biological vulnerabilities linked to gastrointestinal, atopic, and neurodevelopmental outcomes.

The online version contains supplementary material available at 10.1038/s41598-025-34646-4.

## Linked entities

- **Diseases:** constipation (MONDO:0002203), diarrhea (MONDO:0001673), irritable bowel syndrome (MONDO:0005052), attention deficit hyperactivity disorder (MONDO:0007743), major depressive disorder (MONDO:0002009)

## Full-text entities

- **Diseases:** death (MESH:D003643), Dysbiosis (MESH:D064806), abdominal pain disorders (MESH:D015746), sleep difficulties (MESH:D012893), constipation (MESH:D003248), LGA (MESH:D016640), atopic dermatitis (MESH:D003876), allergic rhinitis (MESH:D065631), depression (MESH:D003866), heart disease (MESH:D006331), anxiety (MESH:D001007), IBS (MESH:D043183), mood problems (MESH:D019964), NSD (MESH:D029461), , gut, and systemic inflammation (MESH:D007249), diarrhea (MESH:D003967), allergic diseases (MESH:D004342), congenital anomaly (MESH:D000013), DGBI (MESH:D001927), intestinal obstruction (MESH:D007415), TMCHD (MESH:C562515), postpartum depression (MESH:D019052), disorders of gut (MESH:C536735), migraine (MESH:D008881), behavior problems (MESH:D001523), immune dysregulation (OMIM:614878), Infantile colic (MESH:D003085), long-term disorders (MESH:D000088562), crying (MESH:D003410), atopic disease (MESH:D006969), asthma (MESH:D001249), hyperactivity (MESH:D006948), neurodevelopmental disorders (MESH:D002658), autism spectrum disease (MESH:D000067877), ADHD (MESH:D001289), cow milk protein allergy (MESH:D016269), major depression (MESH:D003865)
- **Chemicals:** DSM17938 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Limosilactobacillus reuteri (species) [taxon 1598]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12868711