Study on the correlation between serum homocysteine and blood lipid levels and white matter lesions in patients with Parkinson's disease
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摘要:
目的 寻找帕金森病(PD)患者并发脑白质病(WML)的危险因素,以及同型半胱氨酸(Hcy)和血脂水平与WML的相关性。 方法 选择2015年1月—2020年1月安徽医科大学第二附属医院神经内科住院的PD患者200例为研究组,同期体检者110例为对照组。对其进行病史和人口学资料采集,测定各组生化指标水平。采用Fazekas分级将研究组分为4组。比较4组间临床资料及生化指标的差异,并应用logistic回归分析以及Spearman相关分析确定PD患者并发WML的影响因素。 结果 研究组Hcy的水平、WML的发生率及严重程度高于对照组,血脂水平低于对照组(均P<0.05);Hcy与WML严重程度呈正相关(r=0.556, P<0.001),在调整了人口学及混杂因素后,Hcy水平与WML严重程度仍呈正相关(r=0.400, P<0.001),Hcy预测PD患者发生WML的AUC为0.717(95%CI:0.673~0.861, P<0.001);WML严重程度与PD患者的H-Y评分、UPDRS运动评分呈正相关(r=0.460、0.360, 均P<0.001)。 结论 血Hcy水平升高可能是PD患者并发WML的独立危险因素,HDL-C水平升高是PD患者并发WML的保护因素;Hcy或可作为PD患者并发WML的一种生物标志物。 Abstract:Objective To find out the risk factors of leukoencephalopathy (WML) in patients with Parkinson's disease (PD) and the correlation between homocysteine levels and WML. Methods From January 2015 to January 2020, 200 patients with PD who were hospitalized in the Department of Neurology of the Second Affiliated Hospital of Anhui Medical University were selected as the study group, and 110 patients with healthy physical examination during the same period were selected as the control group. Medical history and demographic data were collected. The level of biochemical indicators in each group were determined. The Fazekas classification was used to divide the study group into four groups. The differences in clinical data and biochemical indicators between the four groups were compared, and logistic regression analysis and Spearman correlation analysis were used to determine the influencing factors of PD patients with WML. Results The level of Hcy and the incidence and severity of WML in the study group were higher than those of the control group, and the blood lipid level was lower than that of the control group (all P < 0.05), the Hcy and WML were positively correlated (r=0.556, P < 0.001). After adjusting for demographics and confounding factors, the Hcy level was still positively correlated with the severity of WML (r=0.400, P < 0.001). The AUC of Hcy on WML in PD patients was 0.717 (95% CI: 0.673-0.861, P < 0.001); WML severity was positively correlated with PD patients' HY score and UPDRS exercise score (r=0.460, r=0.360, P < 0.001). Conclusion Elevated blood Hcy level may be an independent risk factor for PD patients with WML. Elevated HDL-C level is a protective factor for PD patients with WML. The Hcy may be used as a biomarker for PD patients with WML. -
Key words:
- Parkinson's disease /
- Homocysteine /
- White matter lesions /
- Risk factors
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表 1 2组一般临床资料及血生化指标比较
组别 例数 年龄(x±s,岁) 性别(男/女, 例) 高血压[例(%)] 糖尿病[例(%)] 冠心病[例(%)] 吸烟[例(%)] 饮酒[例(%)] TC(x±s,mmol/L) TG(x±s,mmol/L) 对照组 110 67.24±10.37 44/66 33(30.0) 12(10.9) 13(11.8) 22(20.0) 16(14.5) 4.70±0.96 1.40±0.69 研究组 200 68.86±9.31 99/101 77(38.5) 25(12.5) 16(8.0) 35(17.5) 32(16.0) 4.35±1.04 1.24±0.72 统计量 1.199a 2.590b 2.268b 0.173b 1.186b 0.293b 0.116a -2.903a -1.860a P值 0.231 0.120 0.139 0.719 0.310 0.646 0.870 0.004 0.006 组别 例数 LDL-C(x±s,mmol/L) HDL-C(x±s,mmol/L) 载脂蛋白A(x±s,g/L) 载脂蛋白B(x±s,g/L) 脂蛋白a(x±s,mg/L) Hcy(x±s,μmol/L) 尿酸(x±s,μmol/L) 胱抑素C(x±s,mg/L) 对照组 110 2.93±0.76 1.18±0.25 1.37±0.27 0.89±0.21 270.3±240.4 11.50±2.89 274.7±82.8 0.75±0.29 研究组 200 2.70±0.74 1.19±0.34 1.33±0.31 0.81±0.27 233.6±271.4 14.49±5.57 286.1±94.2 0.80±0.32 统计量 -2.509a 0.560a -8.170a -2.419a -1.183a 4.767a 1.052a 1.153a P值 0.013 0.956 0.414 0.016 0.238 < 0.001 0.294 0.250 注:a为t值,b为χ2值。 表 2 2组脑白质病变发生情况比较[例(%)]
组别 例数 WML 0分 1分 2分 3分 对照组 110 56(50.9) 54(49.1) 52(47.3) 3(2.7) 1(0.9) 研究组 200 157(78.5) 43(21.5) 74(37.0) 48(24.0) 35(17.5) 注:2组WML发生率比较,χ2=67.251,P < 0.001。 表 3 研究组不同程度WML患者的一般临床资料、血生化指标及临床特征比较
组别 例数 年龄(x±s, 岁) 性别(男/女, 例) 高血压[例(%)] 糖尿病[例(%)] 冠心病[例(%)] 吸烟[例(%)] 饮酒[例(%)] 正常组 43 62.70±9.10 16/27 13(30.2) 6(14.0) 2(4.7) 6(14.0) 5(11.6) 轻度病变组 74 68.18±8.80a 35/39 30(40.5) 10(13.5) 8(10.8) 12(16.2) 9(12.2) 中度病变组 48 71.67±7.78a 26/22 25(52.1) 6(12.5) 3(6.2) 8(16.7) 8(16.7) 重度病变组 35 71.90±9.20a 22/13 9(25.7) 3(8.6) 3(8.6) 9(25.7) 10(28.6) 统计量 10.299b 1.902c 2.555c 0.212c 0.548c 0.699c 1.866c P值 < 0.001 0.126 0.055 0.874 0.634 0.577 0.169 组别 例数 TC(x±s,mmol/L) TG(x±s,mmol/L) LDL-C(x±s,mmol/L) HDL-C(x±s,mmol/L) 载脂蛋白A(x±s,g/L) 载脂蛋白B(x±s,g/L) 脂蛋白a(x±s,mg/L) 正常组 43 4.30±0.88 1.31±0.87 2.66±0.65 1.23±0.36 1.41±0.34 0.79±0.20 244.5±256.2 轻度病变组 74 4.58±1.00 1.17±0.67 2.80±0.67 1.28±0.31 1.37±0.28 0.81±0.22 287.6±283.0 中度病变组 48 4.42±1.17 1.28±0.79 2.84±0.83 1.17±0.34 1.31±0.29 0.86±0.30 196.9±164.2 重度病变组 35 3.87±1.00de 1.23±0.52 2.37±0.75 0.99±0.32ade 1.21±0.33ad 0.77±0.39 169.0±121.8 统计量 3.860b 0.359b 3.177b 5.316b 2.752b 0.669b 2.272b P值 0.010 0.783 0.260 0.002 0.044 0.572 0.820 组别 例数 Hcy(x±s,μmol/L) 尿酸(x±s,μmol/L) 胱抑素C(x±s,mg/L) 病程(x±s,年) H-Y分级(x±s,级) UPDRS-Ⅲ(x±s,分) 正常组 43 11.44±5.96c 267.2±80.7 0.63±0.18e 3.21±3.16 1.72±0.57 13.28±3.54 轻度病变组 74 12.50±4.07 282.2±91.3 0.90±0.39a 4.37±3.76 2.16±0.75a 16.73±5.95a 中度病变组 48 15.53±2.60d 301.6±99.3 0.77±0.31d 4.24±3.03 2.43±0.61ad 16.50±3.78a 重度病变组 35 21.00±5.35ade 296.0±107.1 0.83±0.25a 7.37±5.07ade 2.80±0.73ade 19.69±3.80ade 统计量 35.993b 1.161b 6.438b 8.396b 17.728b 22.245b P值 < 0.001 0.326 < 0.001 < 0.001 < 0.001 < 0.001 注:UPDRS-Ⅲ为UPDRS运动评分。与正常组比较,aP<0.05;与轻度病变组比较,dP<0.05;与中度病变组比较,eP<0.05;b为F值,c为χ2值。 表 4 影响WML严重程度的相关因素logistic回归分析
影响因素 B SE Wald χ2 P值 OR值 95%CI Hcy 0.256 0.047 29.955 < 0.001 1.285 1.171~1.410 HDL-C 1.313 0.576 5.205 0.023 0.269 0.087~0.831 -
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