Plasma miR-124 Is a Promising Candidate Biomarker for Human Intracerebral Hemorrhage Stroke.
Plasma miR-124 Is a Promising Candidate Biomarker for Human Intracerebral Hemorrhage Stroke.
复制标题
血浆 miR-124 是人类脑出血中风的有前途的候选生物标志物
DOI:
10.1007/s12035-017-0808-8
复制
发表时间:
2018-07
影响因子:
5.1
通讯作者:
Poon WS
中科院分区:
文献类型:
--
作者:
Wang Z;Lu G;Sze J;Liu Y;Lin S;Yao H;Zhang J;Xie D;Liu Q;Kung HF;Lin MC;Poon WS
Stroke causes death or long-term disabilities and threatens the general health of the population worldwide. Recent studies have suggested that miRNAs are dysregulated and can be used as biomarkers for diagnosis and prognosis in stroke. The intracerebral hemorrhage (ICH) accounts for 15% of all the stroke cases. However, at present, little is known regarding the functions and clinical implications of miRNAs in ICH. In the present study, we established the collagenase-induced rat ICH model to mimic human ICH syndrome. We profiled the expression of 728 rat miRNAs at different time points in rat brain tissues and plasma post-ICH and identified a set human brain-enriched miRNAs that had changed expression level in the plasma of rat ICH. Among them, the expression levels of miR-124 displayed significantly synchronous alterations in rat plasma and brain tissue during ICH progression. They were significantly elevated at the acute injury phase (day 1 and 2), gradually decreased during the delayed recovery phase (day 7, 14 and 30), and finally restored to normal levels at late recovery phase (day 60). We further determined the plasma expression profile of miR-124 from human ICH patients. Similar to the pattern observed in rat ICH model, our results indicated that immediately after patients reached the hospital, the average plasma concentrations of miR-124 increased more than 100-fold in 24 h, then decreased gradually on day 2, 7, 14 and to near normal level on day 30. Taken together, these results strongly suggested that plasma concentration of miR-124 is a promising candidate biomarker for the early detection and predictive prognosis of human ICH.
登录
查看更多内容
影响因子:
8.3
作者:
ELGER, B;SEEGA, J;BRENDEL, R
通讯作者:
BRENDEL, R
影响因子:
9.9
作者:
Rosenberg, GA;Navratil, M
通讯作者:
Navratil, M
影响因子:
168.9
作者:
Qureshi, Adnan I.;Mendelow, A. David;Hanley, Daniel F.
通讯作者:
Hanley, Daniel F.
影响因子:
8.3
作者:
DeBow, SB;Davies, MLA;Colbourne, F
通讯作者:
Colbourne, F
DOI:
10.1016/j.trsl.2015.01.012
发表时间:
2015-08
期刊:
Translational research : the journal of laboratory and clinical medicine
影响因子:
--
作者:
Lenkala D;Gamazon ER;LaCroix B;Im HK;Huang RS
通讯作者:
Huang RS