Neurofilament light is a novel biomarker for mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
21 01 2021
Historique:
received: 11 03 2020
accepted: 07 01 2021
entrez: 22 1 2021
pubmed: 23 1 2021
medline: 28 9 2021
Statut: epublish

Résumé

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a complicated maternally inherited disorder lacking of sensitive and specific biomarkers. The objective of this study was to investigate the serum neurofilament light chain (NfL) as a novel biomarker of neurological dysfunction in MELAS. Patients with different status of MELAS were enrolled in this study. The Mini-Mental State Examination (MMSE) was given to the participants to evaluate cognition status. Multiple functional MRI was performed on the participants. Blood samples were collected and the serum NfL concentrations were determined by the single-molecule array technology (Simoa). This study enrolled 23 patients with MELAS, 15 people in the acute attack phase of MELAS and 10 people in the remission phase, including 2 patients in both acute attack and remission phase. Sixteen healthy controls (HCs) were also enrolled. Serum NfL level increased significantly in patients with MELAS. Serum NfL level in the acute attack group (146.73 [120.91-411.31] pg/ml, median [IQR]) was higher than in the remission group (40.31 [19.54-151.05] pg/ml, median [IQR]) and HCs group (7.70 [6.13-9.78] pg/ml, median [IQR]) (p < 0.05). The level of NfL in the remission phase group was higher than in HCs group (p < 0.05). A negative correlation was found between the serum NfL level and MMSE (p = 0.006, r = -0.650). The NfL concentration correlated positively with stroke-like lesion volume in the brain (r = 0.740, p < 0.001). Serum NfL may serve as a novel biomarker for the neurological dysfunction in MELAS patients.

Identifiants

pubmed: 33479417
doi: 10.1038/s41598-021-81721-7
pii: 10.1038/s41598-021-81721-7
pmc: PMC7819984
doi:

Substances chimiques

Biomarkers 0
Neurofilament Proteins 0
neurofilament protein L 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2001

Commentaires et corrections

Type : ErratumIn

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Auteurs

Yong-Sheng Zheng (YS)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Chong Sun (C)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Rong Wang (R)

Department of Radiology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Ne Chen (N)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Su-Shan Luo (SS)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Jian-Ying Xi (JY)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Jia-Hong Lu (JH)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Chong-Bo Zhao (CB)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Yu-Xin Li (YX)

Department of Radiology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Lei Zhou (L)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China.

Jie Lin (J)

Department of Neurology, Huashan Hospital, Fudan University, 12 Middle Urumqi Road, Shanghai, 200040, China. linjie15@fudan.edu.cn.

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Classifications MeSH