Evidence map›Paper›PMID 35195735›Full record

ArticleDiabetologia2022

Familial aggregation and shared genetic loading for major psychiatric disorders and type 2 diabetes.

Mei-Hsin Su, Ying-Hsiu Shih, Yen-Feng Lin, Pei-Chun Chen, Chia-Yen Chen, Po-Chang Hsiao, Yi-Jiun Pan, Yu-Li Liu, Shih-Jen Tsai, Po-Hsiu Kuo and 3 more

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Article in Diabetologia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

13 authors at 7 institutions in 2 countries.

Mei-Hsin SuDepartment of Occupational Safety and Health, College of Public Health, China Medical University, Taichung, Taiwan.ORCID 0000-0002-7198-4874
Ying-Hsiu ShihDepartment of Public Health, College of Public Health, China Medical University, Taichung, Taiwan.ORCID 0000-0002-3967-784X
Yen-Feng LinCenter for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan.ORCID 0000-0003-3017-6026
Pei-Chun ChenDepartment of Public Health, College of Public Health, China Medical University, Taichung, Taiwan.
Chia-Yen ChenBiogen, Cambridge, MA, USA.ORCID 0000-0001-9548-5597
Po-Chang HsiaoCollege of Public Health, National Taiwan University, Taipei, Taiwan.
Yi-Jiun PanSchool of Medicine, College of Medicine, China Medical University, Taichung, Taiwan.ORCID 0000-0002-2522-7805
Yu-Li LiuCenter for Neuropsychiatric Research, National Health Research Institutes, Miaoli, Taiwan.
Shih-Jen TsaiDepartment of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan.ORCID 0000-0002-9987-022X
Po-Hsiu KuoCollege of Public Health, National Taiwan University, Taipei, Taiwan.ORCID 0000-0003-0365-3587
Chi-Shin WuDepartment of Psychiatry, National Taiwan University Hospital, Taipei, Taiwan.ORCID 0000-0003-2762-7295
Yen-Tsung HuangInstitute of Statistical Science, Academia Sinica, Taipei, Taiwan.ORCID 0000-0001-7657-0040
Shi-Heng WangDepartment of Occupational Safety and Health, College of Public Health, China Medical University, Taichung, Taiwan. wangsh@mail.cmu.edu.tw.ORCID 0000-0002-8466-2698
China Medical University · TWNational Health Research Institutes · TWNational Taiwan University · TWBroad Institute · USInstitute of Statistical Science, Academia Sinica · TWNational Taiwan University Hospital · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisPsychiatric disorders, such as schizophrenia (SCZ), major depressive disorder (MDD) and bipolar disorder (BPD), are highly comorbid with type 2 diabetes. However, the mechanisms underlying such comorbidity are understudied. This study explored the familial aggregation of common psychiatric disorders and type 2 diabetes by testing family history association, and investigated the shared genetic loading between them by testing the polygenic risk score (PRS) association.

methodsA total of 105,184 participants were recruited from the Taiwan Biobank, and genome-wide genotyping data were available for 95,238 participants. The Psychiatric Genomics Consortium-derived PRS for SCZ, MDD and BPD was calculated. Logistic regression was used to estimate the OR with CIs between a family history of SCZ/MDD/BPD and a family history of type 2 diabetes, and between the PRS and the risk of type 2 diabetes.

resultsA family history of type 2 diabetes was associated with a family history of SCZ (OR 1.23, 95% CI 1.08, 1.40), MDD (OR 1.19, 95% CI 1.13, 1.26) and BPD (OR 1.26, 95% CI 1.15, 1.39). Compared with paternal type 2 diabetes, maternal type 2 diabetes was associated with a higher risk of a family history of SCZ. SCZ PRS was negatively associated with type 2 diabetes in women (OR 0.92, 95% CI 0.88, 0.97), but not in men; the effect of SCZ PRS reduced after adjusting for BMI. MDD PRS was positively associated with type 2 diabetes (OR 1.04, 95% CI 1.00, 1.07); the effect of MDD PRS reduced after adjusting for BMI or smoking. BPD PRS was not associated with type 2 diabetes. CONCLUSIONS/

interpretationThe comorbidity of type 2 diabetes with psychiatric disorders may be explained by shared familial factors. The shared polygenic loading between MDD and type 2 diabetes implies not only pleiotropy but also a shared genetic aetiology for the mechanism behind the comorbidity. The negative correlation between polygenic loading for SCZ and type 2 diabetes implies the role of environmental factors.

Indexed as

Diabetes Mellitus, Type 2Major Depressive DisorderMental DisordersFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleBipolar disorderComorbidityDepressionDiabetesFamilial aggregationPolygenic risk scoreSchizophrenia

Identifiers

PMID35195735
OpenAlexW4213109847

What OpenQuestion holds

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Registered trials

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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.