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Role of hyperhomocysteinemia in proliferative diabetic retinopathy: A case–control study

机译:高同型半胱氨酸血症在增生性糖尿病视网膜病变中的作用:病例对照研究

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Purpose: Hyperhomocysteinemia has been postulated as a potential risk factor for the development and progression of diabetic retinopathy. The aim of this study was to determine the association of hyperhomocysteinemia with proliferative diabetic retinopathy (PDR). Methods: This was a hospital-based, case–control study, conducted at a tertiary care ophthalmic center in South India. Thirty-nine patients with proliferative diabetic retinopathy were enrolled as cases, and 39 age- and gender-matched patients with no diabetic retinopathy (No DR) were enrolled as controls. Fasting serum homocysteine estimation, as well as baseline investigations, were done in all participants. Data regarding demographic profile and risk factors were documented. Data were analyzed using Chi-square test and independent t-test, as appropriate. Results: The prevalence of hyperhomocysteinemia was higher in PDR (59%) compared to “No DR” (48.7%); however, this difference was not statistically significant (P = 0.36). Similarly, the mean serum homocysteine level in cases was higher than in controls, but this was not statistically significant (17.98 + 6.26 μmol/L vs. 17.71 + 8.17 μmol/L; P = 0.87). Longer duration of diabetes, hypertension, anemia, and renal dysfunction were found to be significantly associated with PDR. Conclusion: The prevalence of hyperhomocysteinemia as well as the mean serum levels of homocysteine were found to be higher in the cases with PDR, compared to the controls with No DR, although the difference was not statistically significant. Longer duration of diabetes, hypertension, anemia, and renal dysfunction were significantly associated with PDR.
机译:目的:高同型半胱氨酸血症被假定为糖尿病性视网膜病发展和进程的潜在危险因素。这项研究的目的是确定高同型半胱氨酸血症与增生性糖尿病视网膜病变(PDR)的关联。方法:这是一项基于医院的病例对照研究,在印度南部的三级眼科中心进行。 39例糖尿病性增生性视网膜病变患者入组,无糖尿病性视网膜病变(No DR)的39例年龄和性别匹配的患者入选。所有参与者均进行了空腹血清高半胱氨酸估计以及基线研究。记录有关人口概况和风险因素的数据。酌情使用卡方检验和独立t检验分析数据。结果:PDR的高同型半胱氨酸血症的患病率(59%)高于“ No DR”(48.7%);但是,这种差异在统计学上不显着(P = 0.36)。同样,病例中的平均血清高半胱氨酸水平高于对照组,但无统计学意义(17.98 + 6.26μmol/ L与17.71 + 8.17μmol/ L; P = 0.87)。发现糖尿病,高血压,贫血和肾功能不全的持续时间与PDR显着相关。结论:与无DR的对照组相比,PDR的高同型半胱氨酸血症的患病率和平均血清半胱氨酸水平高于无DR的对照组,尽管差异无统计学意义。糖尿病,高血压,贫血和肾功能不全的持续时间与PDR显着相关。

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