Solakivi Tiina, Kunnas Tarja, Nikkari Seppo T
Department of Medical Biochemistry, University of Tampere Medical School and Fimlab Laboratories , Tampere , Finland.
Scand J Clin Lab Invest. 2015 May;75(3):254-8. doi: 10.3109/00365513.2014.1003596. Epub 2015 Feb 27.
Human fatty acid transporter CD36 gene variations have previously been associated with fat preferences and obesity. These variations could thus cause overweight and hypothetically lead to hypertension. The association of CD36 SNP rs1761667 with body mass index (BMI) and hypertension was therefore studied in a Finnish cohort of adults.
The data were collected from the Tampere adult population cardiovascular risk study (TAMRISK). A total of 314 cases with diagnosed hypertension, and 422 non-hypertensive healthy controls were selected from a Finnish periodic 50-year-old health examination cohort. Most subjects had prior health examination data also from their 40- and 45-year examinations. DNA was extracted from buccal swabs and the human CD36 genetic variant was analyzed using KASP genotyping.
The CD36 SNP rs1761667 variant AA was significantly associated with lower BMI, as compared to variants AG and GG at the ages of 40-, 45-, and 50 years (p < 0.001, p = 0.005 and p = 0.013, respectively). No association of this CD36 variation with hypertension was found.
CD36 rs1761667 was associated with BMI in the TAMRISK study. Considering the multitude of roles of CD36 in processes related to fatty acid metabolism and sensing in the body, it is plausible that genetic variation in human fatty acid transporter CD36 can have effects on regulation of energy homeostasis.
人类脂肪酸转运蛋白CD36基因变异先前已与脂肪偏好和肥胖相关联。因此,这些变异可能导致超重,并有可能引发高血压。因此,在芬兰一个成年人群队列中研究了CD36单核苷酸多态性(SNP)rs1761667与体重指数(BMI)和高血压的关联。
数据收集自坦佩雷成年人群心血管风险研究(TAMRISK)。从芬兰定期50岁健康检查队列中选取了314例确诊为高血压的病例和422例非高血压健康对照。大多数受试者还拥有40岁和45岁健康检查的先前数据。从口腔拭子中提取DNA,并使用竞争性等位基因特异性PCR(KASP)基因分型分析人类CD36基因变异。
与40岁、45岁和50岁时的AG和GG变异相比,CD36 SNP rs1761667变异AA与较低的BMI显著相关(分别为p < 0.001, p = 0.005和p = 0.013)。未发现该CD36变异与高血压有关联。
在TAMRISK研究中,CD36 rs1761667与BMI相关。考虑到CD36在体内脂肪酸代谢和感知相关过程中的多种作用,人类脂肪酸转运蛋白CD36的基因变异可能对能量稳态调节产生影响是合理的。