同型半胱氨酸及其代谢关键酶MTHFR C677T基因多态性与阻塞性睡眠呼吸暂停低通气综合征患者合并并发症的相关性OA
Association between homocysteine and MTHFR C677T gene polymorphism with complications in obstructive sleep apnea hypopnea syndrome patients
目的 探讨同型半胱氨酸(homocysteine,Hcy)及其代谢关键酶亚甲基四氢叶酸还原酶C677T基因多态性与阻塞性睡眠呼吸暂停低通气综合征(obstructive sleep apnea hypopnea syndrome,OSAHS)患者合并高血压、2型糖尿病、动脉粥样硬化的相关性.方法 纳入OSAHS患者85例、非OSAHS患者77例,检测患者的基因型和血清Hcy、空腹血糖、糖化血红蛋白水平,同时进行颈部血管超声检测.将Hcy水平≥10 μmol/L定义为高同型半胱氨酸血症(hyperhomocysteinemia,HHcy),比较各基因型患者的血清Hcy水平.比较OSAHS并发症组、单纯OSAHS组、对照组(即无OSAHS且无并发症)的Hcy水平、MTHFR C677T基因多态性、C/T等位基因频率;再采用多因素二元Logistic回归分析,在控制混杂因素的情况下,探讨OSAHS患者合并并发症的独立危险因素.结果 CC、CT、TT基因型患者的Hcy水平分别为10.11(9.15,11.07)、10.86(9.58,11.10)、15.81(11.43,50.76)μmol/L,TT 基因型患者 Hcy水平明显高于CT基因型及CC基因型(均P<0.05).OSAHS并发症组、单纯OSAHS组、对照组的 Hcy 水平分别为 11.16(10.05,13.80)、9.88(9.31,11.41)、10.38(9.29,11.34)μmol/L,OSAHS并发症组Hcy水平明显高于单纯OSAHS组(P<0.05),三组基因多态性及等位基因频率间的差异无统计学意义.控制混杂因素后显示,HHcy是OSAHS人群合并并发症的独立危险因素,OR值(95%CI)为4.682(1.261~17.380).结论 MTHFR C677T基因多态性影响血清Hcy水平,HHcy是OSAHS患者合并并发症的独立危险因素;MTHFR C677T基因多态性及C/T等位基因频率与OSAHS人群合并并发症风险无关.
Objective To investigate the association between homocysteine(Hcy)and the C677T gene polymorphism in its key metabolic enzyme,methylenetetrahydrofolate reductase(MTHFR),and the complications of hypertension,type 2 diabetes mellitus and atherosclerosis in patients with obstructive sleep apnea hypopnea syndrome(OSAHS).Methods A total of 85 OSAHS patients and 77 non-OSAHS patients were enrolled.The genotypes,and levels of serum Hcy,fasting blood glucose and hemoglobin Alc of all subjects were detected,while cervical vascular ultrasound was performed simultaneously.Hcy ≥ 10 μmol/L was defined as hyperhomocysteinemia(HHcy).The serum Hcy levels were compared among patients with different genotypes.The Hcy levels,MTHFR C677T gene polymorphism,and C/T allele frequencies were compared among an OSAHS with complications group,a pure OSAHS group,and a control group(without OSAHS or complications).Then,multivariate binary Logistic regression analysis was performed to identify independent risk factors for complications in OSAHS patients with confounding factors adjusted.Results The Hcy levels in the patients with CC,CT and TT genotypes were 10.11(9.15,11.07),10.86(9.58,11.10)and 15.81(11.43,50.76)μmol/L,respectively.Hcy level in the patients with TT genotype was significantly higher than that in the cases with CT or CC genotypes(both P<0.05).The Hcy levels of the OSAHS with complications group,the pure OSAHS group,and the control group were 11.16(10.05,13.80),9.88(9.31,11.41),and 10.38(9.29,11.34)μmol/L,respectively.The Hcy level of the OSAHS with complications group was significantly higher than that of the pure OSAHS group(P<0.05).There were no statistically significant differences in gene polymorphism or C/T allele frequency among the three groups.After adjusting for confounding factors,it revealed that HHcy was an independent risk factor for concurrent complications in OSAHS patients,and the odds ratio(95% confidence interval)was 4.682(1.261-17.380).Conclusion The MTHFR C677T gene polymorphism affects serum Hcy level.HHcy is an independent risk factor for concurrent complications in OSAHS patients,however,neither the MTHFR C677T gene polymorphism nor the C/T allele frequency were associated with complications in OSAHS patients.
陈尚丽;陈璇;陈若瑾;秦涛;王珍艳;唐智
610100 四川 成都,四川护理职业学院附属医院(四川省第三人民医院)耳鼻咽喉头颈外科||519000 广东佛山,南方医科大学顺德医院(顺德第一人民医院)耳鼻咽喉头颈外科519090 广东 珠海,珠海市第五人民医院耳鼻咽喉科523000 广东东莞,东莞市滨海湾中心医院耳鼻咽喉头颈外科519000 广东佛山,南方医科大学顺德医院(顺德第一人民医院)超声科610100 四川 成都,四川护理职业学院附属医院(四川省第三人民医院)耳鼻咽喉头颈外科528300 广东 佛山,南方医科大学顺德医院附属杏坛医院五官科
医药卫生
阻塞性睡眠呼吸暂停低通气综合征同型半胱氨酸亚甲基四氢叶酸还原酶C677T高血压2型糖尿病动脉粥样硬化
obstructive sleep apnea hypopnea syndromehomocysteinemethylenetetrahydrofolate reductaseC677Thypertensiontype 2 diabetes mellitusatherosclerosis
《实用心电与临床诊疗》 2025 (3)
331-337,7
广东省中医药局中医药科研项目(20241302)佛山市自筹经费类科技创新项目(2220001004878)
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