The Relationship Between Serum VCAM-1 and Alzheimer's Disease in Patients with Type 2 Diabetes Mellitus

被引:9
作者
Zhang, Lingyun [1 ]
Mao, Huawu [2 ]
机构
[1] Zutangshan Hosp, Dept Lab Med, Nanjing 211153, Jiangsu, Peoples R China
[2] Taizhou Second Peoples Hosp, Dept Neurol, Taizhou 225500, Jiangsu, Peoples R China
关键词
diabetes mellitus; Alzheimer's disease; vascular cell adhesion molecule-1; prognostic value; CELL-ADHESION MOLECULE-1; VASCULAR CELL; AIRWAY INFLAMMATION; COGNITIVE DECLINE; EXPRESSION; PROGRESSION; DEMENTIA; MARKERS; CLONING;
D O I
10.2147/DMSO.S274232
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Previous studies have reported that diabetes mellitus (DM) is a risk factor for Alzheimer's disease (AD). Vascular cell adhesion molecule-1 (VCAM-1) plays an important role in the pathological process of atherosclerosis. The aim was to elucidate the relationship between serum VCAM-1 and early AD in DM patients. Methods: Serum samples for VCAM-1 were tested in 208 DM patients. All included DM patients were followed up for a median of 36 months prospectively. The prognostic value of serum VCAM-1 for predicting AD events was analyzed by using Cox proportional hazard. Results: Serum VCAM-1 was independently associated with AD history after adjusting for related confounding factors in patients with DM at baseline by using the logistic regression analysis (OR=1.861; 95% CI, 1.435-2.539; P-trend=0.020). The Cox proportional hazard model suggested that VCAM-1 was a prognostic factor for AD events in the DM patients (HR=2.728; 95% CI, 1.785-5.439; P-trend<0.001). Stratified analysis showed that the significant association between AD event and serum VCAM-1 in DM patients was not affective by CVD history. Conclusion: Our results showed that higher VCAM-1 levels were significantly related to a higher risk of AD events in DM patients. The serum biomarker might be beneficial to predict AD early. Serum VCAM-1 might be a good biochemical parameter for predicting AD in DM.
引用
收藏
页码:4661 / 4667
页数:7
相关论文
共 31 条
[1]  
Al-Ghurabi M. E., 2015, AM J LIFE SCI, V3, P22, DOI DOI 10.11648/J.AJLS
[2]   Adhesion molecules and atherosclerosis [J].
Blankenberg, S ;
Barbaux, S ;
Tiret, L .
ATHEROSCLEROSIS, 2003, 170 (02) :191-203
[3]   Percutaneous transluminal mitral valvuloplasty reduces circulating vascular cell adhesion molecule-1 in rheumatic mitral stenosis [J].
Chen, MC ;
Chang, HW ;
Juang, SS ;
Yip, HK ;
Wu, CJ ;
Yu, TH ;
Cheng, CI .
CHEST, 2004, 125 (04) :1213-1217
[4]   Inhibition of STAT3 phosphorylation by sulforaphane reduces adhesion molecule expression in vascular endothelial cell [J].
Cho, Young S. ;
Kim, Chan H. ;
Ha, Tae S. ;
Ahn, Hee Y. .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2016, 94 (11) :1220-1226
[5]  
Daulatzai MA, 2016, AM J NEURODEGENER DI, V5
[6]   Plasma concentration of soluble vascular cell. Adhesion molecule-1 and subsequent cardiovascular risk [J].
de Lemos, JA ;
Hennekens, CH ;
Ridker, PM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 36 (02) :423-426
[7]   Eosinophilic airway inflammation: role in asthma and chronic obstructive pulmonary disease [J].
George, Leena ;
Brightling, Christopher E. .
THERAPEUTIC ADVANCES IN CHRONIC DISEASE, 2016, 7 (01) :34-51
[8]  
Gibbons M, 2009, THERAPY, V6, P805, DOI [10.2217/thy.09.7716, DOI 10.2217/THY.09.77]
[9]   Angiotensin II receptor blockade reduces tachycardia-induced atrial adhesion molecule expression [J].
Goette, Andreas ;
Bukowska, Alicja ;
Lendeckel, Uwe ;
Erxleben, Michaela ;
Hammwoehner, Matthias ;
Strugala, Denis ;
Pfeiffenberger, Jan ;
Roehl, Friedrich-Wilhelm ;
Huth, Christof ;
Ebert, Matthias P. A. ;
Klein, Helmut U. ;
Roecken, Christoph .
CIRCULATION, 2008, 117 (06) :732-742
[10]  
Hammwöhner M, 2007, EXP BIOL MED, V232, P581