Evidence map›Paper›PMID 36374587›Full record

ArticleCirculation. Genomic and precision medicine2022

Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture.

Alexander E Katz, Min-Lee Yang, Michael G Levin, Catherine Tcheandjieu, Michael Mathis, Kristina Hunker, Susan Blackburn, Jonathan L Eliason, Dawn M Coleman, Natalia Fendrikova-Mahlay and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

27 authors at 14 institutions in 4 countries.

Alexander E Katz *Department of Internal Medicine, Division of Cardiovascular Medicine (A.E.K., M.-L.Y., K.H., H.H., S.K.G.), University of Michigan, Ann Arbor.ORCID 0000-0001-9706-9490
Min-Lee Yang *Department of Internal Medicine, Division of Cardiovascular Medicine (A.E.K., M.-L.Y., K.H., H.H., S.K.G.), University of Michigan, Ann Arbor.ORCID 0000-0003-2823-8320
Michael G Levin *Corporal Michael J. Crescenz Philadelphia VA Medical Center (M.G.L., S.M.D.).ORCID 0000-0002-9937-9932
Catherine TcheandjieuGladstone Institute of data science and Biotechnology, Gladstone Institutes; and Department of epidemiology and biostatistics, University of California at San Francisco, CA. (C.T.).ORCID 0000-0001-9559-4339
Michael MathisDepartment of Anesthesiology, Michigan Medicine (M.M., C.M.B.), University of Michigan, Ann Arbor.ORCID 0000-0002-9697-2212
Kristina HunkerDepartment of Internal Medicine, Division of Cardiovascular Medicine (A.E.K., M.-L.Y., K.H., H.H., S.K.G.), University of Michigan, Ann Arbor.ORCID 0000-0003-1032-4757
Susan BlackburnDepartment of Surgery, Section of Vascular Surgery (S.B., J.L.E., D.M.C., M.K., J.C.S.), University of Michigan, Ann Arbor.
Jonathan L EliasonDepartment of Surgery, Section of Vascular Surgery (S.B., J.L.E., D.M.C., M.K., J.C.S.), University of Michigan, Ann Arbor.
Dawn M ColemanDepartment of Surgery, Section of Vascular Surgery (S.B., J.L.E., D.M.C., M.K., J.C.S.), University of Michigan, Ann Arbor.ORCID 0000-0001-5622-7253
Natalia Fendrikova-MahlayHeart, Vascular and Thoracic Institute, Cleveland Clinic, Cleveland, OH (N.F.-M.).ORCID 0000-0002-0719-0180
Heather L GornikHarrington Heart and Vascular Institute, University Hospitals, Cleveland, OH (H.L.G.).ORCID 0000-0002-5849-4010
Monita KarmakarDepartment of Surgery, Section of Vascular Surgery (S.B., J.L.E., D.M.C., M.K., J.C.S.), University of Michigan, Ann Arbor.
Hannah HillDepartment of Internal Medicine, Division of Cardiovascular Medicine (A.E.K., M.-L.Y., K.H., H.H., S.K.G.), University of Michigan, Ann Arbor.
Chang XuDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor (C.X., M.Z., S.Z., X.Z.).ORCID 0000-0003-2831-1604
Matthew ZawistowskiDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor (C.X., M.Z., S.Z., X.Z.).ORCID 0000-0002-3005-083X
Chad M BrummettDepartment of Anesthesiology, Michigan Medicine (M.M., C.M.B.), University of Michigan, Ann Arbor.
Sebastian ZoellnerDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor (C.X., M.Z., S.Z., X.Z.).ORCID 0000-0001-7362-156X
Xiang ZhouDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor (C.X., M.Z., S.Z., X.Z.).ORCID 0000-0002-4331-7599
Christopher J O'DonnellVA Boston Healthcare System (C.O.).ORCID 0000-0002-2667-8624
Julie A DouglasDepartment of Human Genetics (A.E.K., M.-L.Y., K.H., H.H., J.A.D., J.Z.L., S.K.G.), University of Michigan, Ann Arbor.
Themistocles L AssimesVA Palo Alto Health Care System (T.L.A., P.S.T.).ORCID 0000-0003-2349-0009
Phillip S TsaoVA Palo Alto Health Care System (T.L.A., P.S.T.).ORCID 0000-0002-4331-7599
VA Million Veteran Program
Jun Z LiDepartment of Human Genetics (A.E.K., M.-L.Y., K.H., H.H., J.A.D., J.Z.L., S.K.G.), University of Michigan, Ann Arbor.
Scott M DamrauerCorporal Michael J. Crescenz Philadelphia VA Medical Center (M.G.L., S.M.D.).ORCID 0000-0001-8009-1632
James C StanleyDepartment of Surgery, Section of Vascular Surgery (S.B., J.L.E., D.M.C., M.K., J.C.S.), University of Michigan, Ann Arbor.ORCID 0000-0001-7585-5909
Santhi K GaneshDepartment of Internal Medicine, Division of Cardiovascular Medicine (A.E.K., M.-L.Y., K.H., H.H., S.K.G.), University of Michigan, Ann Arbor.ORCID 0000-0002-3663-5249
Michigan Medicine · USVA Palo Alto Health Care System · USH3D (United States) · USStatistical Service · CYBrigham and Women's Hospital · USPhiladelphia VA Medical Center · USJisc · GBCleveland Clinic · USGladstone Institutes · USInstitute of Human Genetics · PLNational Human Genome Research Institute · USUniversity Hospitals of Cleveland · USUniversity of Michigan · USVA Boston Healthcare System · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024989 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI DAVIS, PAMELA B · 2007 to 2011
$53.7M
Clinical and Translational Science Collaborative of Northern Ohio, Catalyzing Linkages to Equity in Health (CLE Health)UM1TR004528 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI GRACE A MCCOMSEY · 2023 to 2026
$32.1M
Genome-Wide Association Analysis in Essential Hypertension (FEHGAS study)R01HL086694 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ARAVINDA CHAKRAVARTI · 2007 to 2026
$21.2M
Training Program in Cardiovascular Biology and MedicineT32HL007843 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI THOMAS P. CAPPOLA, Sharlene M Day · 1996 to 2026
$11.0M
Genomic and Functional Studies of Dysplasia-Associated Arterial DiseasesR35HL161016 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANTHI K GANESH · 2022 to 2026
$4.6M
Genetic and Genomic Analysis of Arterial DysplasiaR01HL139672 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GANESH, SANTHI K · 2018 to 2021
$2.9M
Precision Cardio-Metabolic Phenotyping for Genetic Discovery and Risk PredictionIK2CX001780 · VA · PHILADELPHIA VA MEDICAL CENTER · PI DAMRAUER, SCOTT MICHAEL · 2018 to 2023
–
BLRD VA I01 BX003362BLRD VA I01 BX004821CSRD VA IK2 CX001780Doris Duke Charitable Foundation 2013104NCATS NIH HHS UM1 TR004528NCRR NIH HHS UL1 RR024989NHLBI NIH HHS R01 HL086694NHLBI NIH HHS R01 HL139672NHLBI NIH HHS R35 HL161016NHLBI NIH HHS T32 HL007843
6 · The paper itself

Abstract

backgroundThe risk of arterial diseases may be elevated among family members of individuals having multifocal fibromuscular dysplasia (FMD). We sought to investigate the risk of arterial diseases in families of individuals with FMD.

methodsFamily histories for 73 probands with FMD were obtained, which included an analysis of 463 total first-degree relatives focusing on FMD and related arterial disorders. A polygenic risk score for FMD (PRS

resultsOf all first degree relatives of probands, 9.3% were diagnosed with FMD, aneurysms, and dissections. Aneurysmal disease occurred in 60.5% of affected relatives and 5.6% of all relatives. Among 227 female first-degree relatives of probands, 4.8% (11) had FMD, representing a relative risk (RR)

conclusionsFMD and AAAs seem to be sex-dimorphic manifestations of a heritable arterial disease with a partially shared complex genetic architecture. Excess risk of having an AAA according to a family history of FMD may justify screening in family members of individuals having FMD.

Indexed as

Aortic Aneurysm, AbdominalFibromuscular DysplasiaArteriesFemaleGenome-Wide Association StudyHumansMaleRisk Factorsaneurysmaortic aneurysm, abdominalarteriesdissectionfibromuscular dysplasiageneticssex dimorphism

Identifiers

PMID36374587
PMCPMC9772208
OpenAlexW4308953975

What OpenQuestion holds

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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.