Analysis of influencing factors in patients with ischemic leukodystrophy
YE Xin1 LIU Shihua2 ZHANG Chao2 ZHONG Ping2▲
1.Department of General Practice, Suzhou Hospital of Anhui Medical University, Anhui Province, Suzhou 234000, China;
2.Department of Neurology, Suzhou Hospital of Anhui Medical University, Anhui Province, Suzhou 234000, China
Abstract:Objective To investigate the influencing factors of disease progression in patients with white matter ischemic lesions (WMIL). Methods Clinical data of 215 patients with WMIL admitted to Suzhou Hospital of Anhui Medical University from June 2017 to September 2021 were collected. The degree of leukodystrophy was assessed according to the Fazekas scale; the control group (100 cases) had normal brain MRI. The serum concentration of asymmetric dimethylarginine (ADMA) was determined by enzyme-related immunosorbent assay. The clinical data and ADMA concentration of the two groups were compared to analyze the influencing factors of ischemic white matter lesions and the relationship between serum ADMA and the degree of white matter lesions. Results The proportion of hypertension and type 2 diabetes in WMIL group was higher than that in control group, while the serum ADMA concentration in light, medium and heavy WMIL group were higher than that in control group, and the differences were statistically significant (P<0.05). Spearman rank correlation analysis showed that serum ADMA concentration in WMIL group was positively correlated with Fazekas score (r=0.850, P<0.01). Multivariate logistic analysis showed that hypertension, diabetes history, and elevated serum ADMA were independent risk factors for WMIL progression (OR>1, P<0.05). Conclusion High concentration of ADMA is an independent factor affecting the progression of WMIL, and the higher the concentration, the more severe the degree of leukoencephalopathy.
[1] Son DH,Lee HS,Lee YJ. Association between serum carbohydrate antigen 19-9 levels and leukoaraiosis in middle- aged and older adults:A cross-sectional study [J]. Atherosclerosis,2020,292:188-192.
[2] Wu XQ,Ya JY,Zhou D,et al. Pathogeneses and Imaging Features of Cerebral White Matter Lesions of Vascular Origins [J]. Aging Dis,2021,12(8):2031-2051.
[3] Grosse GM,Schwedhelm E,Worthmann H,et al. Arginine Derivatives in Cerebrovascular Diseases:Mechanisms and Clinical Implications [J]. Int J Mol Sci,2020,21(5):1798.
[4] Choi S,Singh I,Singh AK,et al. Asymmetric dimethylarginine exacerbates cognitive dysfunction associated with cerebrovascular pathology [J]. FASEB J,2020,34(5):6808- 6823.
[5] Janes F,Cifù A,Pessa ME,et al. ADMA as a possible marker of endothelial damage. A study in young asymptomatic patients with cerebral small vessel disease [J]. Sci Rep,2019,9(1):14207.
[6] Rufa A,Blardi P,De Lalla A,et al. Plasma levels of asymmetric dimethylarginine in cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy [J]. Cerebrovascular diseases (Basel,Switzerland),2008,26(6):636-640.
[7] Galluzzi S,Lanni C,Pantoni L,et al. White matter lesions in the elderly:pathophysiological hypothesis on the effect on brain plasticity and reserve [J]. J Neurol Sci,2008,273(1- 2):3-9.
[8] 杨紫葵.缺血性脑白质病变与认知功能、外周血抗- MOG抗体、ICAM-1的临床关系研究[D].合肥:安徽医科大学,2017.
[9] Lin J,Wang DL,Lan LF,et al. Multiple Factors Involved in the Pathogenesis of White Matter Lesions [J]. BioMed research international,2017,2017:9372050.
[10] 张国芳,刘安祥,张骏.ADMA在短暂性脑缺血发作发病机制中的研究进展[J].海南医学,2021,32(23):3111-3114.
[11] Gao Q,Fan Y,Mu LY,et al. S100B and ADMA in cerebral small vessel disease and cognitive dysfunction [J]. J Neurol Sci,2015,354(1/2):27-32.
[12] Watson CP,Pazarentzos E,Fidanboylu M,et al. The transporter and permeability interactions of asymmetric dimethylarginine (ADMA) and L-arginine with the human blood- brain barrier in vitro [J]. Brain Res,2016,1648(Pt A):232-242.
[13] Appel D,Seeberger M,Schwedhelm E,et al. Asymmetric and Symmetric Dimethylarginines are Markers of Delayed Cerebral Ischemia and Neurological Outcome in Patients with Subarachnoid Hemorrhage [J]. Neurocrit Care,2018, 29(1):84-93.
[14] 洪铭,范鹰,宋志强.ADMA/DDAH系统与脑白质疏松症的关系[J].中华老年多器官疾病杂志,2016,15(8):637-640.
[15] Hoth KF,Tate DF,Poppas A,et al. Endothelial function and white matter hyperintensities in older adults with cardiovascular disease [J]. Comparative Study,2007,38(2):308-312.
[16] 马芬芬,王彦,朱映红,等.原发性高血压合并急性脑梗死患者血清非对称性二甲基精氨酸与血脂水平的变化及相关性研究[J].名医,2021(7):92-93.
[17] Chung JW,Oh MJ,Cho YH,et al. Distinct Roles of Endothelial dysfunction and Inflammation in Intracranial Atherosclerotic Stroke [J]. European Neurology,2017,77(3/4):211-219.
[18] 袁华容,吴建平,黄家俊.血清L-Arg,ADMA水平与急性脑梗死患者静脉溶栓疗效的相关性分析[J].卒中与神经疾病,2021,28(1):25-28.
[19] Yuji H,Tomoya K,Kazunori K. Testosterone Deficiency and Endothelial Dysfunction:Nitric Oxide,Asymmetric Dimethylarginine,and Endothelial Progenitor Cells [J]. Sexual Medicine Reviews,2019,7(4):661-668.
[20] Yao H,Takashima Y,Mori T,et al. Hypertension and white matter lesions are independently associated with apathetic behavior in healthy elderly subjects:the Sefuri brain MRI study [J]. Hypertens Res,2009,32(7):586-590.
[21] Ferik S,Güven H,Ate■ MP,et al. Diabetic polyneuropathy,deep white matter lesions,and carotid atherosclerosis:is there any association? [J]. Neurol Sci,2018,39(1):103-110.
[22] Verhaaren BF,Vernooij MW,de Boer R,et al. High blood pressure and cerebral white matter lesion progression in the general population [J]. Hypertension,2013,61(6):1354- 1359.
[23] 王萍,唐敏,夏仕勇,等.高龄糖尿病患者缺血性脑白质病变严重程度及其危险因素分析[J].中华老年心脑血管病杂志,2020,22(2):197-199.
[24] 毛竹青,俞春江,付锦.血管危险因素对脑白质病变作用研究的进展[J].心血管康复医学杂志,2019,28(6):794-796.
[25] Guan J,Yan C,Gao Q,et al. Analysis of risk factors in patients with leukoaraiosis [J]. Medicine (Baltimore),2017, 96(8):e6153.