Genome-Wide Linkage and Regional Association Study of Blood Pressure Response to the Cold Pressor Test in Han Chinese

Author:

Yang Xueli1,Gu Dongfeng1,He Jiang1,Hixson James E.1,Rao Dabeeru C.1,Lu Fanghong1,Mu Jianjun1,Jaquish Cashell E.1,Chen Jing1,Huang Jianfeng1,Shimmin Lawrence C.1,Rice Treva K.1,Chen Jichun1,Wu Xigui1,Liu Depei1,Kelly Tanika N.1

Affiliation:

1. From the Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA (X.Y., J.H., J.C., T.N.K.); State Key Laboratory of Cardiovascular Disease, Department of Epidemiology and Population Genetics, Fuwai Hospital, National Center of Cardiovascular Diseases (X.Y., D.G., J.H., J.C., X.W.) and National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences (D.L.), Chinese Academy of Medical Sciences and Peking Union Medical College,...

Abstract

Background— Blood pressure (BP) response to cold pressor test (CPT) is associated with increased risk of cardiovascular disease. We performed a genome-wide linkage scan and regional association analysis to identify genetic determinants of BP response to CPT. Methods and Results— A total of 1961 Chinese participants completed the CPT. Multipoint quantitative trait linkage analysis was performed, followed by single-marker and gene-based analyses of variants in promising linkage regions (logarithm of odds ≥2). A suggestive linkage signal was identified for systolic BP response to CPT at 20p13 to 20p12.3, with a maximum multipoint logarithm of odds score of 2.37. On the basis of regional association analysis with 1351 single nucleotide polymorphisms in the linkage region, we found that marker rs2326373 at 20p13 was significantly associated with mean arterial pressure responses to CPT ( P =8.8×10 −6 ) after false discovery rate adjustment for multiple comparisons. A similar trend was also observed for systolic BP response ( P =0.03) and diastolic BP response ( P =4.6×10 −5 ). Results of gene-based analyses showed that variants in genes MCM8 and SLC23A2 were associated with systolic BP response to CPT ( P =4.0×10 −5 and 2.7×10 −4 , respectively), and variants in genes MCM8 and STK35 were associated with mean arterial pressure response to CPT ( P =1.5×10 −5 and 5.0×10 −5 , respectively). Conclusions— Within a suggestive linkage region on chromosome 20, we identified a novel variant associated with BP responses to CPT. We also found gene-based associations of MCM8 , SLC23A2 , and STK35 in this region. Additional work is warranted to confirm these findings. Clinical Trial Registration— URL: http://www.clinicaltrials.gov ; Unique identifier: NCT00721721.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),Cardiology and Cardiovascular Medicine,Genetics

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