Evidence map›Paper›PMID 40421265›Full record

ArticleJournal of inflammation research2025

Guillain-Barré Syndrome During the Outbreak of Omicron in Southern China: A Multicenter Case-Control Study.

Mengcui Gui, Peicai Fu, Lijun Luo, Qunhui Liu, Jun Chen, Zhongmou Han, Liying Chang, Hui Chen, Daokai Gong, Juan Chen and 8 more

Abstract read
In one paragraph

Article in Journal of inflammation research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Mengcui GuiDepartment of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.
Peicai FuDepartment of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.
Lijun LuoDepartment of Neurology, Wuhan Hospital of Traditional Chinese and Western Medicine, Wuhan, Hubei, 430022, People's Republic of China.
Qunhui LiuDepartment of Neurology, the Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi Clinical College of Wuhan University, Enshi, Hubei, 445099, People's Republic of China.
Jun ChenDepartment of Neurology, Taihe Hospital, Affiliated Hospital of Hubei University of Medicine, Shiyan, Hubei, 442099, People's Republic of China.
Zhongmou HanDepartment of Neurology, Yichang Central People's Hospital, 1st Affiliated Hospital of China Three Gorges University, Yichang, Hubei, 443002, People's Republic of China.
Liying ChangDepartment of Neurology, Xiangyang Central Hospital, Hubei University of Arts and Science, Xiangyang, Hubei, 441106, People's Republic of China.
Hui ChenDepartment of Neurology, the People's Hospital of Laifeng County, Enshi, Hubei, 445799, People's Republic of China.
Daokai GongDepartment of Neurology, Jingzhou Central Hospital, Yangtze University, Jingzhou, Hubei, 441021, People's Republic of China.
Juan ChenDepartment of Neurology, Minda Hospital of Hubei Minzu University, Enshi, Hubei, 445099, People's Republic of China.
Yafang LiuDepartment of Neurology, Huangshi Central Hospital, Hubei Polytechnic University, Huangshi, Hubei, 435000, People's Republic of China.
Rong ZhangDepartment of Neurology, Hubei Aerospace Hospital, Xiaogan, Hubei, 432009, People's Republic of China.ORCID 0000-0003-3793-6550
Ming ZhangDepartment of Neurology, Jingmen Hospital of Traditional Chinese Medicine, Jingmen, Hubei, 448001, People's Republic of China.
Mingqing XiangDepartment of Neurology, the First People's Hospital of Jingzhou, 1st Affiliated Hospital of Yangtze University, Jingzhou, Hubei, 434000, People's Republic of China.
Xiaohua YangDepartment of Neurology, the First People's Hospital of Tianmen, Affiliated Hospital of Hubei University of Science and Technology, Tianmen, Hubei, 431701, People's Republic of China.
Jing LinDepartment of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.
Bitao BuDepartment of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.
Zhijun LiDepartment of Neurology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The largest nationwide outbreak of Omicron, a severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) variant, occurred between December 2022 and February 2023 in China. This multicenter case-control study investigated the clinical features of GBS during this period. Methods: The clinical characteristics of patients diagnosed with GBS associated with SARS-CoV-2 were assessed during an Omicron outbreak at 14 referral hospitals in Hubei Province, Southern China. In the case-control study, patients with GBS were identified and diagnosed between 2021 and 2022 at Tongji Hospital in Wuhan, Hubei province. Results: Forty-one patients were diagnosed with GBS during the Omicron outbreak. The median patient age was 57.5 years, and 51.2% were male. The median period between the preceding infection and onset of neurological symptoms was 10 days. The majority of the patients (38 cases [92.7%]) presented with classic sensorimotor neuropathy, with the lower limbs involved more often; 17 cases (41.5%) were accompanied by cranial neuropathies, which was most observed with the bilateral or unilateral facial paralysis (13 cases [31.7%]). Albuminocytologic dissociation was observed in 27 patients (71.1%), and mild pleocytosis was found in five patients (12.2%), with a maximum of 22 cells/mm Conclusion: The characteristics of SARS-CoV-2-associated GBS during the Omicron outbreak appear clinically as sensorimotor neuropathy, with a predominant electrophysiological axonal form. A mainly classic post-infectious immune-mediated mechanism may be involved in this process, such as a temporal profile of clinical symptoms, axon-associated autoantibodies, and improvement by immunotherapy.

Indexed as

axonal variantsGuillain–Barré syndromeimmune-mediated mechanismomicronpost-infectioussensorimotor neuropathy

Identifiers

PMID40421265
PMCPMC12105641

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