Evidence map›Paper›PMID 42446714›Full record

ArticleEuropean child & adolescent psychiatry2026

Involvement of adiponectin in the biology of attention deficit hyperactivity disorder.

Nagahide Takahashi, Toshiki Iwabuchi, Tomoko Nishimura, Akemi Okumura, Taeko Harada, Md Shafiur Rahman, Kenji J Tsuchiya

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Article in European child & adolescent psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Nagahide TakahashiDepartment of Neurodevelopmental Disorders, National Center of Neurology and Psychiatry, 4-1-1, Ogawahigashi-Cho, Kodaira, Tokyo, 187-8553, Japan. nagahide.takahashi@ncnp.go.jp.ORCID http://orcid.org/0000-0002-7711-0297
Toshiki IwabuchiResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Tomoko NishimuraResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Akemi OkumuraResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Taeko HaradaResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Md Shafiur RahmanResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Kenji J TsuchiyaResearch Center for Child Mental Development, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the involvement of adiponectin in the development of attention-deficit/hyperactivity disorder (ADHD), using a multi-pronged approach integrating cord blood adiponectin concentrations, polygenic risk scores derived from publicly available GWAS summary statistics, and Mendelian randomization. This study aimed to evaluate both upstream genetic influences and downstream adiponectin-level associations. Using a combination of longitudinal cord blood data (N = 531) and genome-wide association studies of ADHD (N = 55,374) and adiponectin (N = 46,434), we examined observational, genetic, and associations linking adiponectin with ADHD. Lower cord blood adiponectin levels were associated with higher ADHD symptoms at ages 5-6 and 8-9, and predicted membership in the increasing-symptom trajectory group. Gene-set analysis demonstrated pathway-level overlap between ADHD and adiponectin regulation. Genetic correlation analysis showed a significant negative correlation between ADHD and adiponectin levels. Mendelian randomization provided stronger evidence for an association of ADHD on adiponectin levels. Polygenic risk score analysis also demonstrated a negative association between genetic liability for ADHD and cord blood adiponectin levels. Additionally, lower adiponectin levels were found to be associated with elevated inflammatory markers in the cord blood samples obtained from the cohort study, which may provide a potential explanation for the higher prevalence of metabolic comorbidities observed in individuals with ADHD. These findings suggest that adiponectin may be associated with the biologyof ADHD and targeting adiponectin regulation may offer a novel approach for managing ADHD and its related health risks.

Indexed as

ADHDAdiponectinGWASMendelian RandomizationObesityPRS

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.