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Effects of Ninjurin 2 polymorphisms on susceptibility to coronary heart disease.
Yan, Yuping; Du, Xiaoyan; Dou, Xia; Li, Jingjie; Zhang, Wenjie; Yang, Shuangyu; Meng, Wenting; Tian, Gang.
Affiliation
  • Yan Y; Department of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
  • Du X; Department of Cardiovascular Medicine, Xi'an Daxing Hospital, Xi'an, Shaanxi, China.
  • Dou X; Department of Cardiovascular Medicine, First Hospital of Yulin City, Yulin, Shaanxi, China.
  • Li J; Ministry of Education, Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Xi'an, Shaanxi, China.
  • Zhang W; Ministry of Education, Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Xi'an, Shaanxi, China.
  • Yang S; Ministry of Education, Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Xi'an, Shaanxi, China.
  • Meng W; Ministry of Education, Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Xi'an, Shaanxi, China.
  • Tian G; Ministry of Education, Key Laboratory of Resource Biology and Biotechnology in Western China (Northwest University), Xi'an, Shaanxi, China.
Cell Cycle ; 23(3): 328-337, 2024 Feb.
Article de En | MEDLINE | ID: mdl-38512812
ABSTRACT

OBJECTIVE:

The aim of this study was to explore the effects of Ninjurin 2 (NINJ2) polymorphisms on susceptibility to coronary heart disease (CHD).

METHODS:

We conducted a case-control study with 499 CHD cases and 505 age and gender-matched controls. Five single nucleotide polymorphisms (SNPs) in NINJ2 (rs118050317, rs75750647, rs7307242, rs10849390, and rs11610368) were genotyped by the Agena MassARRAY platform. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using logistic regression analysis to assess the association of NINJ2 polymorphisms and CHD risk-adjusted for age and gender. What's more, risk genes and molecular functions were screened via protein-protein interaction (PPI) network and functional enrichment analysis.

RESULTS:

Rs118050317 in NINJ2 significantly increased CHD risk in people aged more than 60 years and women. Rs118050317 and rs7307242 had strong relationships with hypertension risk in CHD patients. Additionally, rs75750647 exceedingly raised diabetes risk in cases under multiple models, whereas rs10849390 could protect CHD patients from diabetes in allele, homozygote, and additive models. We also observed two blocks in NINJ2. Further interaction network and enrichment analysis showed that NINJ2 played a greater role in the pathogenesis and progression of CHD.

CONCLUSION:

Our results suggest that NINJ2 polymorphisms are associated with CHD risk.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Molécules d'adhérence cellulaire neuronale / Maladie coronarienne / Prédisposition génétique à une maladie / Polymorphisme de nucléotide simple Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Cell Cycle Année: 2024 Type de document: Article Pays d'affiliation: Chine

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Molécules d'adhérence cellulaire neuronale / Maladie coronarienne / Prédisposition génétique à une maladie / Polymorphisme de nucléotide simple Limites: Aged / Female / Humans / Male / Middle aged Langue: En Journal: Cell Cycle Année: 2024 Type de document: Article Pays d'affiliation: Chine