Atherosclerosis and cardiovascular involvement in celiac disease: the role of autoimmunity and inflammation

被引:0
作者
Santoro, L. [1 ]
De Matteis, G. [1 ]
Fuorlo, M. [1 ]
Giupponi, B. [1 ]
Martone, A. M. [2 ]
Landi, F. [2 ]
Landolfi, R. [1 ]
Santoliquido, A. [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Sch Med, Dept Internal & Emergency Med, Rome, Italy
[2] Univ Cattolica Sacro Cuore, Sch Med, Dept Geriatr Neurosci & Orthoped, Rome, Italy
关键词
Inflammation; Celiac disease; Atherosclerosis; Carotid artery intima-media thickness; Endothelial dysfunction; Arterial stiffness; INTIMA-MEDIA THICKNESS; CAROTID-ARTERY INTIMA; TISSUE TRANSGLUTAMINASE; ENDOTHELIAL DYSFUNCTION; VASCULAR-DISEASE; INCREASED RISK; DIAGNOSIS; GLUTEN; COHORT; CARDIOMYOPATHY;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: The aim of this review is to explore the evidence about the association among celiac disease (CD), atherosclerosis (AS) and cardiovascular (CV) diseases, and the role of inflammation in this connection. MATERIALS AND METHODS: A systematic literature search was conducted using PubMed, EMBASE, and Cochrane Library for the association among CD, AS and CV diseases. RESULTS: Several studies reported the association of CD with accelerated AS, as evidenced by the alterations of a number of parameters indicative of subclinical AS, as increased carotid artery intima-media thickness, endothelial dysfunction and increased arterial stiffness. In addition, recent evidence reported an increase of CV diseases prevalence in CD patients respect to controls, many of which including ischemic diseases as acute myocardial infarction and angina pectoris, as well as death from ischemic heart disease, and, more rarely, stroke for cerebrovascular involvement. Other not-ischemic CV diseases associated with CD are represented by dilated cardiomyopathy, atrial fibrillation, and myocarditis. CONCLUSIONS: On the basis of the reported association among CD, AS and CV diseases, we suggest to perform a more detailed CV risk assessment in all CD patients than what is currently being achieved in clinical practice, in order to scan and treat modifiable CV risk factors in these patients. In particular, we suggest to resort to instrumental techniques to detect AS in the subclinical stage, in order to prevent AS development and CV diseases in CD patients.
引用
收藏
页码:5437 / 5444
页数:8
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