Inflammatory Burden and Immunomodulative Therapeutics of Cardiovascular Diseases.
Inflammatory Burden and Immunomodulative Therapeutics of Cardiovascular Diseases.
复制标题
DOI:
10.3390/ijms23020804
复制
发表时间:
2022-01-12
影响因子:
5.6
通讯作者:
Huang CC
中科院分区:
文献类型:
--
作者:
Kao TW;Huang CC
Phenotyping cardiovascular illness and recognising heterogeneities within are pivotal in the contemporary era. Besides traditional risk factors, accumulated evidence suggested that a high inflammatory burden has emerged as a key characteristic modulating both the pathogenesis and progression of cardiovascular diseases, inclusive of atherosclerosis and myocardial infarction. To mechanistically elucidate the correlation, signalling pathways downstream to Toll-like receptors, nucleotide oligomerisation domain-like receptors, interleukins, tumour necrosis factor, and corresponding cytokines were raised as central mechanisms exerting the effect of inflammation. Other remarkable adjuvant factors include oxidative stress and secondary ferroptosis. These molecular discoveries have propelled pharmaceutical advancements. Statin was suggested to confer cardiovascular benefits not only by lowering cholesterol levels but also by attenuating inflammation. Colchicine was repurposed as an immunomodulator co-administered with coronary intervention. Novel interleukin-1β and −6 antagonists exhibited promising cardiac benefits in the recent trials as well. Moreover, manipulation of gut microbiota and associated metabolites was addressed to antagonise inflammation-related cardiovascular pathophysiology. The gut-cardio-renal axis was therein established to explain the mutual interrelationship. As for future perspectives, artificial intelligence in conjunction with machine learning could better elucidate the sequencing of the microbiome and data mining. Comprehensively understanding the interplay between the gut microbiome and its cardiovascular impact will help identify future therapeutic targets, affording holistic care for patients with cardiovascular diseases.
登录
查看更多内容
影响因子:
--
作者:
Guo S;Huang Z;Liu X;Zhang J;Ye P;Wu C;Lu S;Jia S;Zhang X;Chen X;Wang M;Wu J
通讯作者:
Wu J
影响因子:
3.5
作者:
Iyer RP;Patterson NL;Zouein FA;Ma Y;Dive V;de Castro Brás LE;Lindsey ML
通讯作者:
Lindsey ML
影响因子:
120.7
作者:
de Lemos, JA;Blazing, MA;Braunwald, E
通讯作者:
Braunwald, E
DOI:
10.1074/jbc.m111.324988
发表时间:
2012-04-20
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
Chang MY;Chan CK;Braun KR;Green PS;O'Brien KD;Chait A;Day AJ;Wight TN
通讯作者:
Wight TN
影响因子:
6.9
作者:
Daseke, Michael J., II;Tenkorang, Mavis A. A.;Lindsey, Merry L.
通讯作者:
Lindsey, Merry L.