Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk.
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Georgakis Marios K, Malik Rainer, Bounkari Omar El, Hasbani Natalie R, Li Jiang, Huffman Jennifer E, Shakt Gabrielle, Tack Reinier W P, Kimball Tamara N, Asare Yaw, Morrison Alanna C, Tsao Noah L, Judy Renae, Mitchell Braxton D, Xu Huichun, Montasser May E, Do Ron, Kenny Eimear E, Loos Ruth J F, Terry James G, Carr John Jeffrey, Bis Joshua C, Psaty Bruce M, Longstreth W T, Young Kendra A, Lutz Sharon M, Cho Michael H, Broome Jai, Khan Alyna T, Wang Fei Fei, Heard-Costa Nancy, Seshadri Sudha, Vasan Ramachandran S, Palmer Nicholette D, Freedman Barry I, Bowden Donald W, Yanek Lisa R, Kral Brian G, Becker Lewis C, Peyser Patricia A, Bielak Lawrence F, Ammous Farah, Carson April P, Hall Michael E, Raffield Laura M, Rich Stephen S, Post Wendy S, Tracy Russel P, Taylor Kent D, Guo Xiuqing, Mahaney Michael C, Curran Joanne E, Blangero John, Clarke Shoa L, Haessler Jeffrey W, Hu Yao, Assimes Themistocles L, Kooperberg Charles, Bernhagen Jürgen, Anderson Christopher D, Damrauer Scott M, Zand Ramin, Rotter Jerome I, de Vries Paul S, Dichgans Martin
Аннотация
METHODS: Computationally predicted damaging or loss-of-function (REVEL > 0.5) variants within CCR2 were detected in whole-exome-sequencing data from 454,775 UK Biobank participants and tested for association with cardiovascular endpoints in gene-burden tests. Given the key role of CCR2 in monocyte mobilization, variants associated with lower monocyte count were prioritized for experimental validation. The response to CCL2 of human cells transfected with these variants was tested in migration and cAMP assays. Validated damaging variants were tested for association with cardiovascular endpoints, atherosclerosis burden, and vascular risk factors. Significant associations were replicated in six independent datasets (n = 1,062,595).
RESULTS: Carriers of 45 predicted damaging or loss-of-function CCR2 variants (n = 787 individuals) were at lower risk of myocardial infarction and coronary artery disease. One of these variants (M249K, n = 585, 0.15% of European ancestry individuals) was associated with lower monocyte count and with both decreased downstream signaling and chemoattraction in response to CCL2. While M249K showed no association with conventional vascular risk factors, it was consistently associated with a lower risk of myocardial infarction (odds ratio [OR]: 0.66, 95% confidence interval [CI]: 0.54-0.81, p = 6.1 × 10-5) and coronary artery disease (OR: 0.74, 95%CI: 0.63-0.87, p = 2.9 × 10-4) in the UK Biobank and in six replication cohorts. In a phenome-wide association study, there was no evidence of a higher risk of infections among M249K carriers.
CONCLUSIONS: Carriers of an experimentally confirmed damaging CCR2 variant are at a lower lifetime risk of myocardial infarction and coronary artery disease without carrying a higher risk of infections. Our findings provide genetic support for the translational potential of CCR2-targeting as an atheroprotective approach.