Precision Medicine for Obesity Program, Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic, Rochester, MN.
Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN.
Mayo Clin Proc. 2023 Apr;98(4):533-540. doi: 10.1016/j.mayocp.2022.10.028. Epub 2022 Dec 20.
To study differences in cardiovascular risk factors and diseases between patients with and without genetic variants in the leptin-melanocortin pathway.
A cross-sectional study of patients with a history of severe obesity genotyped in June 2019 as participants of the Mayo Clinic Biobank was conducted in March 2022 to assess differences in cardiovascular risk and diseases between carriers of a heterozygous variant in the leptin-melanocortin pathway and noncarriers. Cardiovascular risk factors included hypertension, diabetes, dyslipidemia, and smoking. Cardiovascular disease includes coronary artery disease, peripheral artery disease, and cerebrovascular accidents. Patients with a history of bariatric surgery were excluded. We used logistic regression models to estimate the odds ratio and 95% CI, adjusting for age, body mass index (BMI), and sex.
Among a total of 168 carriers (8%; 121 [72%] female; mean [SD] age, 65.1 [14.9] years; BMI, 44.0 [7.4] kg/m) and 2039 noncarriers (92%; 1446 [71%] female; mean [SD] age, 64.9 [14.4] years; BMI, 42.9 [6.6] kg/m), carriers had higher prevalence odds of hypertension (odds ratio, 3.26; 95% CI, 2.31 to 4.61; P<.001) and reported higher number of cardiovascular risk factors compared with noncarriers (2.4 [1.1] vs 2.0 [1.1]; P<.001). There were no significant differences in the adjusted odds associated with diabetes, dyslipidemia, smoking, or cardiovascular disease.
Despite having similar body weight and BMI, carriers of heterozygous variants in the leptin-melanocortin pathway had higher rates of hypertension than noncarriers. These findings point to an association between hypertension and leptin-melanocortin pathway variants.
研究瘦素-黑素皮质素途径基因变异患者与无基因变异患者心血管危险因素和疾病的差异。
对 2019 年 6 月作为梅奥诊所生物库参与者进行过严重肥胖基因分型的患者进行了一项横断面研究,以评估瘦素-黑素皮质素途径杂合变异携带者与非携带者之间心血管风险和疾病的差异。心血管危险因素包括高血压、糖尿病、血脂异常和吸烟。心血管疾病包括冠状动脉疾病、外周动脉疾病和脑血管意外。排除有减重手术史的患者。我们使用逻辑回归模型估计比值比和 95%置信区间,调整年龄、体重指数(BMI)和性别。
在总共 168 名携带者(8%;121 名[72%]女性;平均[SD]年龄 65.1[14.9]岁;BMI 44.0[7.4]kg/m)和 2039 名非携带者(92%;1446 名[71%]女性;平均[SD]年龄 64.9[14.4]岁;BMI 42.9[6.6]kg/m)中,携带者高血压的患病率更高(比值比 3.26;95%置信区间 2.31 至 4.61;P<.001),与非携带者相比,报告的心血管危险因素更多(2.4[1.1]与 2.0[1.1];P<.001)。糖尿病、血脂异常、吸烟或心血管疾病的调整后比值无显著差异。
尽管体重和 BMI 相似,瘦素-黑素皮质素途径杂合变异携带者的高血压发生率高于非携带者。这些发现表明高血压与瘦素-黑素皮质素途径变异之间存在关联。