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中华脑血管病杂志(电子版) ›› 2023, Vol. 17 ›› Issue (05) : 458 -463. doi: 10.11817/j.issn.1673-9248.2023.05.006

临床研究

高水平脂蛋白(a)与无“三高”老年人群小动脉硬化型脑小血管病的相关性研究
晏美娟(), 邵礼晖   
  1. 221000 江苏徐州,徐州医科大学附属徐州市立医院神经内科
    221400 江苏新沂,新沂市中医院康复科
  • 收稿日期:2022-12-17 出版日期:2023-10-01
  • 通信作者: 晏美娟
  • 基金资助:
    2021年徐州市基础研究计划面上项目(KC21063); 中国矿业大学青年基金项目(2020QN83); 徐州医科大学附属医院科技发展基金项目(XYFY2020034)

Correlation between lipoprotein (a) and arteriosclerotic cerebral small vessel disease in elderly population without diabetes, hyperlipidemia and hypertension

Meijuan Yan(), Lihui Shao   

  1. Department of Neurology, Xuzhou Municipal Hospital Affiliated to Xuzhou Medical University, Xuzhou 221000, China
    Department of Rehabilitation, Xinyi Traditional Chinese Medicine Hospital, Xinyi 221400, China
  • Received:2022-12-17 Published:2023-10-01
  • Corresponding author: Meijuan Yan
引用本文:

晏美娟, 邵礼晖. 高水平脂蛋白(a)与无“三高”老年人群小动脉硬化型脑小血管病的相关性研究[J]. 中华脑血管病杂志(电子版), 2023, 17(05): 458-463.

Meijuan Yan, Lihui Shao. Correlation between lipoprotein (a) and arteriosclerotic cerebral small vessel disease in elderly population without diabetes, hyperlipidemia and hypertension[J]. Chinese Journal of Cerebrovascular Diseases(Electronic Edition), 2023, 17(05): 458-463.

目的

探讨脂蛋白(a)与同时排除高血压病、高脂血症、糖尿病(简称无“三高”)老年人群小动脉硬化型脑小血管病(aCSVD)的相关性。

方法

回顾性纳入徐州医科大学附属徐州市立医院神经内科2016年1月至2021年7月收治住院的aCSVD患者2000例(aCSVD组),按年龄、性别,以1∶2比例配对,选择同期体检中心排除aCSVD的体检者为对照组(非aCSVD组,4000例),根据是否有“三高”史,分出无“三高”亚组(aCSVD组=198,non-aCSVD=396)。对比分析病例组和对照组的相关临床资料,并采用多变量Logistic回归模型分析老年人群及无“三高”老年人群aCSVD的危险因素。

结果

在匹配年龄、性别后,老年人群aCSVD组较对照组具有较高比例的高血压病史(56.50% vs 55.16%,χ2=1.548,P=0.006)、糖尿病史(42.50% vs 30.00%,χ2=6.796,P=0.009)及高脂血症史(33.50% vs 31.50%,χ2=7.614,P=0.006),差异均有统计学意义;脂蛋白(a)水平高于对照组,但差异无统计学意义[(0.32±0.11)g/L vs(0.31±0.12)g/L,t=1.876,P=0.061]。多变量Logistic回归分析显示高血压史、糖尿病史可能是老年人群aCSVD的独立危险因素,脂蛋白(a)不是其危险因素。在进行亚组分析时,无“三高”老年人群aCSVD组脂蛋白(a)水平较对照组显著升高,差异有统计学意义[(0.56±0.17)g/L vs (0.49±0.14)g/L,t=5.339,P<0.001]。进一步多变量Logistic回归分析,结果显示脂蛋白(a)是无“三高”老年人群aCSVD的独立危险因素(OR=1.672,95%CI:1.144~2.317,P=0.007)。

结论

脂蛋白(a)是无“三高”老年人群aCSVD的独立危险因素,可作为预测其发病风险的血清生物学标志物。

Objective

To investigate the correlation between lipoprotein (a) and arteriosclerotic cerebral small vessel disease (aCSVD) in the elderly population without hypertension,hyperlipidemia, or diabetes (abbreviated "no three high").

Methods

2000 patients with aCSVD admitted to Department of Neurology of Xuzhou Municipal Hospital Affiliated to Xuzhou Medical University from January 2016 to July 2021 were retrospectively included. Select 4000 cases of the medical check-up who were excluded from aCSVD at the physical examination center during the same period as the control group. The patients were matched by age,sex with a 1∶2 ratio (aCSVD=2000, non aCSVD=4000), and were divided into "no three high" subgroup (aCSVD=198, non aCSVD=396) according to whether they were "no three high" elderly population. The relevant clinical data of the case group and the control group was collected for comparative analysis, and multivariate Logistic regression model was used to analyze the risk factors of aCSVD in the general elderly population and the elderly population without diabetes, hyperlipidemia, and hypertension.

Results

This study showed that after matching the age and gender, the elderly aCSVD group had a higher proportion of hypertension (56.50% vs 55.16%, χ2=1.548, P=0.006), diabetes (42.50% vs 30.00%, χ2=6.796, P=0.009), and hyperlipidemia (33.50% vs 31.50%, χ2=7.614, P=0.006) than the control group, and the differences were statistically significant. The level of lipoprotein (a) in aCSVD group was higher than that in the control group, but there was no statistical difference [(0.32±0.11) g/L vs (0.31±0.12) g/L, t=1.876, P=0.061]. Logistic regression analysis showed that the history of hypertension and diabetes may be an independent risk factor for aCSVD in the elderly, but lipoprotein (a) was not an independent risk factor for aCSVD. In the subgroup analysis, the level of lipoprotein (a) in the "no three high" elderly population with aCSVD was significantly higher than that in the control group, with a statistically significant difference [(0.56±0.17) g/L vs (0.49±0.14) g/L, t=5.339, P<0.001]. Logistic regression analysis showed that lipoprotein (a) was an independent risk factor for aCSVD in the "no three high" elderly population (OR=1.672, 95%CI: 1.144-2.317, P=0.007).

Conclusion

Lipoprotein (a) is an independent risk factor of aCSVD in the elderly population without diabetes, hyperlipidemia and hypertension, and it can be used as a serum biomarker to predict the risk of aCSVD.

表1 老年人群aCSVD组与对照组临床资料比较
表2 Logistic回归模型分析老年人群aCSVD的危险因素
表3 无“三高”老年人群aCSVD组与非aCSVD组临床资料比较
表4 Logistic回归模型分析无“三高”人群aCSVD的危险因素
1
Zhu R, Li Y, Chen L, et al. Total burden of cerebral small vessel disease on MRI may predict cognitive impairment in Parkinson's disease [J]. Clin Med, 2022, 11(18): 531-538.
2
Wardlaw JM, Smith C, Dichgans M. Small vessel disease: mechanisms and clinical implications [J]. Lancet Neurol, 2019, 18(7): 684-696.
3
Li T, Huang Y, Cai W, et al. Age-related cerebral small vessel disease and inflammaging [J]. Cell Death Dis, 2020, 11(10): 932-937.
4
Zotin MCZ, Sveikata L, Viswanathan A, et al. Cerebral small vessel disease and vascular cognitive impairment: from diagnosis to management [J]. Curr Opin Neurol, 2021, 34(2): 246-257.
5
Gencer B, Mach F. Potential of lipoprotein(a)-lowering strategies in treating coronary artery disease [J]. Drugs, 2020, 80(3): 229-239.
6
中华医学会糖尿病学分会. 中国2型糖尿病防治指南 (2020年版) [J]. 中华糖尿病杂志, 2021, 13(4): 315-409.
7
Arora P, Kalra R, Callas PW, et al. Lipoprotein (a) and risk of ischemic stroke in the REGARDS study [J]. Arterioscler Thromb Vasc Bio, 2019, 39(4): 810-818.
8
Berman AN, Blankstein R. Current and future role of lipoprotein(a) in preventive cardiology [J]. Curr Opin Cardiol, 2019, 34(5): 514-518.
9
Georgakis MK, Malik R, Anderson CD, et al. Genetic determinants of blood lipids and cerebral small vessel disease: role of high-density lipoprotein cholesterol [J]. Brain, 2020, 143(2): 597-610.
10
Rzechorzek NM, Thrippleton MJ, Chappell FM, et al. A daily temperature rhythm in the human brain predicts survival after brain injury [J]. Brain, 2022, 145(6): 2031-2048.
11
Berglund L, Kim K, Zhang W, et al. Lp(a)-associated oxidized phospholipids in healthy black and white participants in relation to apo(a) size, age, and family structure [J]. Am Heart Assoc, 2021, 10(17): e020158.
12
Labudovic D, Kostovska I, Trajkovska KT, et al. Lipoprotein(a)–Link between Atherogenesis and Thrombosis [J]. Prague Med Rep, 2019, 120(23): 39-51.
13
Yeang C, Gordts PL, Tsimikas S. Novel Lipoprotein(a) catabolism pathway via Apolipoprotein(a) recycling adding the plasminogen receptor PlgR (KT) to the list [J]. Circ Res, 2017, 120(7): 1050-1052.
14
Mesgari-Abbasi M, Mahmoudinezhad M, Farhangi MA. Soluble P-selectin, procalcitonin, transforming growth factor (TGF)-β and apo-proteins in association with the components of metabolic syndrome in obese individuals [J]. Clin Nutr ESPEN, 2021, 41(19): 386-390.
15
Liu H, Fu D, Luo Y, et al. Independent association of Lp(a) with platelet reactivity in subjects without statins or antiplatelet agents [J]. Sci Rep, 2022, 12(1): 16609.
16
Schnitzler JG, Hoogeveen RM, Ali L, et al. Atherogenic Lipoprotein(a) increases vascular glycolysis, thereby facilitating inflammation and leukocyte extravasation [J]. Circ Res, 2020, 126(10): 1346-1359.
17
Kostner KM, Kostner GM. Lp(a) and the risk for cardiovascular disease: focus on the Lp(a) paradox in diabetes mellitus [J]. Int J Mol Sci, 2022, 23(7): 3584.
18
Pan Y, Li H, Wang Y, et al. Causal effect of Lp(a) [Lipoprotein(a)] level on ischemic stroke and Alzheimer disease [J]. Stroke, 2019, 50(12): 3532-3539.
19
Tang Y, Geng D. Associations of plasma LP(a), Hcy and D-D levels with the subtype of ischemic cerebrovascular disease [J]. Medicine (Baltimore), 2019, 98(11): e14910-14914.
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