KIF5A and the contribution of susceptibility genotypes as a predictive biomarker for multiple sclerosis.
KIF5A and the contribution of susceptibility genotypes as a predictive biomarker for multiple sclerosis.
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KIF5A和易感基因型作为多发性硬化症的预测生物标志物的贡献。
DOI:
10.1007/s00415-020-10373-w
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发表时间:
2021-06
影响因子:
6
通讯作者:
Wilkins A
中科院分区:
文献类型:
--
作者:
Hares K;Kemp K;Loveless S;Rice CM;Scolding N;Tallantyre E;Robertson N;Wilkins A
There is increasing interest in the development of multiple sclerosis (MS) biomarkers that reflect central nervous system tissue injury to determine prognosis. We aimed to assess the prognostic value of kinesin superfamily motor protein KIF5A in MS by measuring levels of KIF5A in cerebrospinal fluid (CSF) combined with analysis of single nucleotide polymorphisms (SNPs; rs12368653 and rs703842) located within a MS susceptibility gene locus at chromosome 12q13–14 region. Enzyme-linked immunosorbent assay was used to measure KIF5A in CSF obtained from two independent biobanks comprising non-inflammatory neurological disease controls (NINDC), clinically isolated syndrome (CIS) and MS cases. CSF KIF5A expression was significantly elevated in progressive MS cases compared with NINDCs, CIS and relapsing–remitting MS (RRMS). In addition, levels of KIF5A positively correlated with change in MS disease severity scores (EDSS, MSSS and ARMSSS), in RRMS patients who had documented disease progression at 2-year clinical follow-up. Copies of adenine risk alleles (AG/AA; rs12368653 and rs703842) corresponded with a higher proportion of individuals in relapse at the time of lumbar puncture (LP), higher use of disease-modifying therapies post LP and shorter MS duration. Our study suggests that CSF KIF5A has potential as a predictive biomarker in MS and further studies into the potential prognostic value of analysing MS susceptibility SNPs should be considered. The online version of this article (10.1007/s00415-020-10373-w) contains supplementary material, which is available to authorized users.
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DOI:
10.1093/brain/awx370
发表时间:
2018-03-01
期刊:
Brain : a journal of neurology
影响因子:
--
作者:
Brenner D;Yilmaz R;Müller K;Grehl T;Petri S;Meyer T;Grosskreutz J;Weydt P;Ruf W;Neuwirth C;Weber M;Pinto S;Claeys KG;Schrank B;Jordan B;Knehr A;Günther K;Hübers A;Zeller D;Kubisch C;Jablonka S;Sendtner M;Klopstock T;de Carvalho M;Sperfeld A;Borck G;Volk AE;Dorst J;Weis J;Otto M;Schuster J;Del Tredici K;Braak H;Danzer KM;Freischmidt A;Meitinger T;Strom TM;Ludolph AC;Andersen PM;Weishaupt JH;German ALS network MND-NET
通讯作者:
German ALS network MND-NET
影响因子:
3.3
作者:
Semra, YK;Seidi, OA;Sharief, MK
通讯作者:
Sharief, MK
影响因子:
56.9
作者:
Patsopoulos, Nikolas A.;Baranzini, Sergio E.;De Jager, Philip L.
通讯作者:
De Jager, Philip L.
影响因子:
6.4
作者:
Schirmer, Lucas;Antel, Jack P.;Stadelmann, Christine
通讯作者:
Stadelmann, Christine
影响因子:
30.8
作者:
Bahlo, Melanie;Booth, David R.;Willoughby, Ernest
通讯作者:
Willoughby, Ernest