Evidence map›Paper›PMID 33704461›Full record

ArticleHuman molecular genetics2021

Fate or coincidence: do COPD and major depression share genetic risk factors?

Victoria L Martucci, Bradley Richmond, Lea K Davis, Timothy S Blackwell, Nancy J Cox, David Samuels, Digna Velez Edwards, Melinda C Aldrich

Open access · greenAbstract read
In one paragraph

Article in Human molecular genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Relationship between serum Th1/Th2 imbalance and depression in elderly patients with COPD and its clinical implications.Technology and health care : official journal of the European Society for Engineering and Medicine · 2023
    Article
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

8 authors at 2 institutions in 1 country.

Victoria L MartucciVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Bradley RichmondDepartment of Veterans Affairs Medical Center, Nashville, TN 37212, USA.
Lea K DavisVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Timothy S BlackwellDepartment of Veterans Affairs Medical Center, Nashville, TN 37212, USA.
Nancy J CoxVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
David SamuelsVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Digna Velez EdwardsVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Melinda C AldrichVanderbilt Genetics Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Vanderbilt University · USVanderbilt University Medical Center · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
Medical Scientist Training ProgramT32GM152284 · NIGMS · VANDERBILT UNIVERSITY · PI Christopher S. Williams · 2024 to 2026
$4.8M
Training Program on Genetic Variation and Human PhenotypesT32GM080178 · NIGMS · VANDERBILT UNIVERSITY · PI COX, NANCY J, SAMUELS, DAVID C · 2007 to 2021
$3.1M
Mental health and chronic disease: A psycheMERGE investigation into the shared biology underlying psychiatric disorders and their physical comorbiditiesR56MH120736 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DAVIS, LEA K · 2019 to 2020
$1.6M
Unraveling the Complexities of COPD: Modeling COPD Outcomes and Phenotype Associations Using Electronic Health RecordsF30HL140756 · NHLBI · VANDERBILT UNIVERSITY · PI MARTUCCI, VICTORIA · 2018 to 2020
$109k
Role of p73 in COPD PathogenesisIK2BX003841 · VA · VETERANS HEALTH ADMINISTRATION · PI RICHMOND, BRADLEY WINSTON · 2019 to 2023
–
Mechanisms driving airway inflammation in chronic lung diseaseI01BX002378 · VA · VETERANS HEALTH ADMINISTRATION · PI Timothy S. Blackwell · 2014 to 2026
–
BLRD VA I01 BX002378BLRD VA IK2 BX003841NCATS NIH HHS UL1 TR002243NHLBI NIH HHS F30 HL140756NIGMS NIH HHS T32 GM007347NIGMS NIH HHS T32 GM080178NIGMS NIH HHS T32 GM152284NIMH NIH HHS R56 MH120736
6 · The paper itself

Abstract

Major depressive disorder (MDD) is a common comorbidity in chronic obstructive pulmonary disease (COPD), affecting up to 57% of patients with COPD. Although the comorbidity of COPD and MDD is well established, the causal relationship between these two diseases is unclear. A large-scale electronic health record clinical biobank and genome-wide association study summary statistics for MDD and lung function traits were used to investigate potential shared underlying genetic susceptibility between COPD and MDD. Linkage disequilibrium score regression was used to estimate genetic correlation between phenotypes. Polygenic risk scores (PRS) for MDD and lung function traits were developed and used to perform a phenome-wide association study (PheWAS). Multi-trait-based conditional and joint analysis identified single-nucleotide polymorphisms (SNPs) influencing both lung function and MDD. We found genetic correlations between MDD and all lung function traits were small and not statistically significant. A PRS-MDD was significantly associated with an increased risk of COPD in a PheWAS [odds ratio (OR) = 1.12, 95% confidence interval (CI): 1.09-1.16] when adjusting for age, sex and genetic ancestry, but this relationship became attenuated when controlling for smoking history (OR = 1.08, 95% CI: 1.04-1.13). No significant associations were found between the lung function PRS and MDD. Multi-trait-based conditional and joint analysis identified three SNPs that may contribute to both traits, two of which were previously associated with mood disorders and COPD. Our findings suggest that the observed relationship between COPD and MDD may not be driven by a strong shared genetic architecture.

Indexed as

Polymorphism, Single NucleotideAdultAgedComorbidityFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLinkage DisequilibriumMajor Depressive DisorderMaleMiddle AgedMultifactorial InheritancePhenotypePulmonary Disease, Chronic ObstructiveRisk Factors

Identifiers

PMID33704461
PMCPMC8120137
OpenAlexW3134688599

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.