神经梅毒对糖尿病和高血压及高血脂的相关性

Correlation between neurosyphilis and diabetes, hypertension and hyperlipidemia

  • 摘要: 目的 探讨神经梅毒对糖尿病、高血压及高血脂之间的相关性。方法 应用快速血浆反应素试验和梅毒螺旋体明胶颗粒凝集试验进行梅毒血清学检测。测定脑脊液白细胞计数并检测患者脑脊液蛋白质、血液糖化血红蛋白、空腹血糖、甘油三酯、总胆固醇、脂蛋白(a)、高密度脂蛋白、低密度脂蛋白、载脂蛋白A1及载脂蛋白B等生化指标。比较神经梅毒患者和非感染性中枢神经系统疾病患者的糖尿病、高血压及高血脂相关指标。结果 神经梅毒的糖尿病患病率、空腹血糖及糖化血红蛋白水平与非感染性中枢神经系统疾病差异无统计学意义;神经梅毒的高血压患病率、收缩压及3级高血压患者比例分别为45.00%(36/80)、138(117,150)mmHg和17.50%(14/80),均高于非感染性中枢神经系统疾病(P<0.05);神经梅毒高脂血症患病率、总胆固醇、低密度脂蛋白和载脂蛋白B分别为20.00%(16/80)、4.32(3.77,5.26)mmol/L、3.03(2.48,3.81)mmol/L和0.87(0.75,1.08)mmol/L,均高于非感染性中枢神经系统疾病患者(P<0.05)。结论 神经梅毒可能导致代谢紊乱,对于神经梅毒患者,应及时关注未来可能发生的代谢紊乱,进行及早干预,以免延误治疗。

     

    Abstract: OBJECTIVE To investigate the association between neurosyphilis and diabetes mellitus, hypertension and dyslipidaemia. METHODS The serological detection of syphilis were performed by rapid plasma reagin test and Treponema pallidum gelatin granule agglutination test. The white blood cell count in cerebrospinal fluid was measured by automatic blood cell analyzer. Biochemical indicators such as the cerebrospinal fluid protein, blood glycosylated hemoglobin, fasting blood glucose, triglyceride, total cholesterol, lipoprotein(a), high density lipoprotein, low density lipoprotein, apolipoprotein A1 and apolipoprotein B were measured by automatic biochemical analyzer. Diabetes, hypertension, and dyslipidaemia-related factors were compared between patients with neurosyphilis and non-infectious central nervous system diseases. RESULTS The prevalence of diabetes mellitus, fasting blood glucose and glycosylated hemoglobin levels of neurosyphilis are not significantly different from non-infectious central nervous system diseases. The prevalence of hypertension, systolic blood pressure and grade 3 hypertension in patients with neurosyphilis were 45.00%(36/80), 138(117,150)mmHg and 17.50%(14/80), respectively, significantly higher than those in patients with non-infectious central nervous system diseases(P<0.05). The prevalence of hyperlipidemia, total cholesterol, low density lipoprotein and apolipoprotein B in patients with neurosyphilis were 20.00%(16/80), 4.32(3.77,5.26) mmol/L, 3.03(2.48,3.81) mmol/L and 0.87(0.75,1.08) mmol/L, respectively, significantly higher than those in patients with non-infectious central nervous system diseases(P<0.05). CONCLUSION Neurosyphilis might lead to metabolic disorders. For patients with neurosyphilis, timely attention should be paid to possible metabolic disorders in the future and early intervention should be performed to avoid delay in treatment.

     

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