Evidence map›Paper›PMID 30729689›Full record

ReviewAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2019

Co-shared genetics and possible risk gene pathway partially explain the comorbidity of schizophrenia, major depressive disorder, type 2 diabetes, and metabolic syndrome.

Teodor T Postolache, Laura Del Bosque-Plata, Serge Jabbour, Michael Vergare, Rongling Wu, Claudia Gragnoli

Abstract readReview
In one paragraph

Review in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

60 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Teodor T PostolacheMood and Anxiety Program, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland.
Laura Del Bosque-PlataNational Institute of Genomic Medicine, Nutrigenetics and Nutrigenomic Laboratory, Mexico City, Mexico.
Serge JabbourDivision of Endocrinology, Diabetes, and Metabolic Disease, Department of Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.
Michael VergareDepartment of Psychiatry and Human Behavior, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.
Rongling WuDepartment of Public Health Sciences, Penn State College of Medicine, Hershey, Pennsylvania.
Claudia GragnoliDivision of Endocrinology, Diabetes, and Metabolic Disease, Department of Medicine, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania.ORCID 0000-0002-3873-6617

Funding

Constitutive and Agent-Based Multiscale Models to Improve Vein Graft SurvivalU01HL119178 · NHLBI · UNIVERSITY OF FLORIDA · PI BERCELI, SCOTT A, GARBEY, MARC · 2013 to 2018
$2.7M
Chronic Toxoplasma gondii, Pregnancy reactivation, and Perinatal DepressionR01HD086805 · NICHD · UNIVERSITY OF SOUTH FLORIDA · PI GROER, MAUREEN EDITH · 2017 to 2021
$2.6M
Genetic Neuro-Endocrine Role in Depression and Type 2 DiabetesR01HD086911 · NICHD · THOMAS JEFFERSON UNIVERSITY · PI GRAGNOLI, CLAUDIA · 2016 to 2020
$1.5M
Role of Kynurenine Pathway Metabolites in Perinatal Depression and SuicidalityR01MH104622 · NIMH · VAN ANDEL RESEARCH INSTITUTE · PI BRUNDIN, LENA CECILIA · 2014 to 2016
$1.2M
Toxoplasma gondi, the kynurenine pathway, and suicidal behavior in veteransI01CX001310 · VA · BALTIMORE VA MEDICAL CENTER · PI POSTOLACHE, TEODOR T · 2016 to 2020
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Alfred P. Sloan Foundation G-2016-7077American Foundation for Suicide Prevention 1I01CX001310-01American Foundation for Suicide Prevention DIG-1-162-12CSR&D Merit AwardCSRD VA I01 CX001310Eunice Kennedy Shriver National Institute Of Child Health & Human Development 1I01CX001310-01 CSR&D Merit AwardNHLBI NIH HHS U01 HL119178NICHD NIH HHS R01 HD086805NICHD NIH HHS R01 HD086911NIMH NIH HHS R01 MH104622U.S. Food and Drug Administration FDU.001418-19
6 · The paper itself

Abstract

Schizophrenia (SCZ) and major depressive disorder (MDD) in treatment-naive patients are associated with increased risk for type 2 diabetes (T2D) and metabolic syndrome (MetS). SCZ, MDD, T2D, and MetS are often comorbid and their comorbidity increases cardiovascular risk: Some risk genes are likely co-shared by them. For instance, transcription factor 7-like 2 (TCF7L2) and proteasome 26S subunit, non-ATPase 9 (PSMD9) are two genes independently reported as contributing to T2D and SCZ, and PSMD9 to MDD as well. However, there are scarce data on the shared genetic risk among SCZ, MDD, T2D, and/or MetS. Here, we briefly describe T2D, MetS, SCZ, and MDD and their genetic architecture. Next, we report separately about the comorbidity of SCZ and MDD with T2D and MetS, and their respective genetic overlap. We propose a novel hypothesis that genes of the prolactin (PRL)-pathway may be implicated in the comorbidity of these disorders. The inherited predisposition of patients with SCZ and MDD to psychoneuroendocrine dysfunction may confer increased risk of T2D and MetS. We illustrate a strategy to identify risk variants in each disorder and in their comorbid psychoneuroendocrine and mental-metabolic dysfunctions, advocating for studies of genetically homogeneous and phenotype-rich families. The results will guide future studies of the shared predisposition and molecular genetics of new homogeneous endophenotypes of SCZ, MDD, and metabolic impairment.

Indexed as

ComorbidityDiabetes Mellitus, Type 2EndophenotypesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMajor Depressive DisorderMaleMetabolic SyndromeNeuroimmunomodulationPhenotypePolymorphism, Single NucleotideProlactinRisk FactorsProlactinMajor Depressive DisorderMetabolic SyndromeProlactin and Oxytocin Gene PathwaySchizophreniaType 2 Diabetes

Identifiers

PMID30729689
PMCPMC6492942

What OpenQuestion holds

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Read underepoch 390

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.