Searching the Resource Information Network

Our searching services are busy right now. Please try again later

  • Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

Association of PHACTR1 with Coronary Artery Calcium Differs by Sex and Cigarette Smoking.

Kirsten Voorhies | Kendra Young | Fang-Chi Hsu | Nicholette D Palmer | Merry-Lynn N McDonald | Sanghun Lee | Georg Hahn | Julian Hecker | Dmitry Prokopenko | Ann Chen Wu | Elizabeth A Regan | Dawn DeMeo | Greg L Kinney | James D Crapo | Michael H Cho | Edwin K Silverman | Christoph Lange | Matthew J Budoff | John E Hokanson | Sharon M Lutz
Journal of cardiovascular development and disease | 2024

Background: Coronary artery calcium (CAC) is a marker of subclinical atherosclerosis and is a complex heritable trait with both genetic and environmental risk factors, including sex and smoking. Methods: We performed genome-wide association (GWA) analyses for CAC among all participants and stratified by sex in the COPDGene study (n = 6144 participants of European ancestry and n = 2589 participants of African ancestry) with replication in the Diabetes Heart Study (DHS). We adjusted for age, sex, current smoking status, BMI, diabetes, self-reported high blood pressure, self-reported high cholesterol, and genetic ancestry (as summarized by principal components computed within each racial group). For the significant signals from the GWA analyses, we examined the single nucleotide polymorphism (SNP) by sex interactions, stratified by smoking status (current vs. former), and tested for a SNP by smoking status interaction on CAC. Results: We identified genome-wide significant associations for CAC in the chromosome 9p21 region [CDKN2B-AS1] among all COPDGene participants (p = 7.1 × 10-14) and among males (p = 1.0 × 10-9), but the signal was not genome-wide significant among females (p = 6.4 × 10-6). For the sex stratified GWA analyses among females, the chromosome 6p24 region [PHACTR1] had a genome-wide significant association (p = 4.4 × 10-8) with CAC, but this signal was not genome-wide significant among all COPDGene participants (p = 1.7 × 10-7) or males (p = 0.03). There was a significant interaction for the SNP rs9349379 in PHACTR1 with sex (p = 0.02), but the interaction was not significant for the SNP rs10757272 in CDKN2B-AS1 with sex (p = 0.21). In addition, PHACTR1 had a stronger association with CAC among current smokers (p = 6.2 × 10-7) than former smokers (p = 7.5 × 10-3) and the SNP by smoking status interaction was marginally significant (p = 0.03). CDKN2B-AS1 had a strong association with CAC among both former (p = 7.7 × 10-8) and current smokers (p = 1.7 × 10-7) and the SNP by smoking status interaction was not significant (p = 0.40). Conclusions: Among current and former smokers of European ancestry in the COPDGene study, we identified a genome-wide significant association in the chromosome 6p24 region [PHACTR1] with CAC among females, but not among males. This region had a significant SNP by sex and SNP by smoking interaction on CAC.

Pubmed ID: 39057616

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

None found

Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL113264
  • Agency: NHLBI NIH HHS, United States
    Id: R00 HL121087
  • Agency: National Heart, Lung and Blood Institute,
    Id: R00HL121087
  • Agency: National Heart, Lung and Blood Institute,
    Id: R01HL089897
  • Agency: National Heart, Lung and Blood Institute,
    Id: R01HL113264
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL089856
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL089856
  • Agency: NIMH NIH HHS, United States
    Id: R01MH129337
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL105339
  • Agency: National Heart, Lung and Blood Institute,
    Id: U01HL089856
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK071891
  • Agency: NIAID NIH HHS, United States
    Id: 75N93023D00011
  • Agency: General Clinical Research Center of Wake Forest School of Medicine,
    Id: M01-RR-07122
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL092301
  • Agency: NIMH NIH HHS, United States
    Id: R01 MH129337
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL089897
  • Agency: NIH HHS, United States
    Id: R01 HL092301
  • Agency: NIH HHS, United States
    Id: R01 HL067348
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL089897
  • Agency: NIH HHS, United States
    Id: R01 AG058921
  • Agency: NIA NIH HHS, United States
    Id: R01 AG058921
  • Agency: National Heart, Lung and Blood Institute,
    Id: R01HL089856
  • Agency: NHLBI NIH HHS, United States
    Id: 75N92021D00011
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL067348
  • Agency: National Heart, Lung and Blood Institute,
    Id: P01HL105339
  • Agency: NIH HHS, United States
    Id: R01 DK071891
  • Agency: NHLBI NIH HHS, United States
    Id: 75N90023D00011
  • Agency: NCRR NIH HHS, United States
    Id: M01 RR007122
  • Agency: National Heart, Lung and Blood Institute,
    Id: U01HL089897

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

This is a list of tools and resources that we have found mentioned in this publication.


PLINK (tool)

RRID:SCR_001757

Open source whole genome association analysis toolset, designed to perform range of basic, large scale analyses in computationally efficient manner. Used for analysis of genotype/phenotype data. Through integration with gPLINK and Haploview, there is some support for subsequent visualization, annotation and storage of results. PLINK 1.9 is improved and second generation of the software.

View all literature mentions