Evidence map›Paper›PMID 38793066›Full record

ArticleJournal of personalized medicine2024

The Presence of Ganglionic Acetylcholine Receptor Antibodies in Sera from Patients with Functional Gastrointestinal Disorders: A Preliminary Study.

Shunya Nakane, Akihiro Mukaino, Yoshiaki Okumura, Hiroaki Hirosawa, Osamu Higuchi, Hidenori Matsuo, Mosaburo Kainuma, Yuji Nakatsuji

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Shunya NakaneDepartment of Neurology, Faculty of Medicine, University of Toyama, Toyama 930-0194, Japan.ORCID 0000-0003-1958-095X
Akihiro MukainoDepartment of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.ORCID 0000-0001-7486-0597
Yoshiaki OkumuraOkumura Forest-All Clinic, Otsu 520-0831, Japan.
Hiroaki HirosawaDepartment of Neurology, Faculty of Medicine, University of Toyama, Toyama 930-0194, Japan.
Osamu HiguchiDepartment of Neurology and Clinical Research, National Hospital Organization Nagasaki Kawatana Medical Center, Nagasaki 859-3615, Japan.
Hidenori MatsuoDepartment of Neurology and Clinical Research, National Hospital Organization Nagasaki Kawatana Medical Center, Nagasaki 859-3615, Japan.ORCID 0000-0003-4115-2310
Mosaburo KainumaDepartment of Japanese Oriental Medicine, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Toyama 930-0194, Japan.
Yuji NakatsujiDepartment of Neurology, Faculty of Medicine, University of Toyama, Toyama 930-0194, Japan.

Funding

Japan Society for the Promotion of Science 19H03549Japan Society for the Promotion of Science 19K17012
6 · The paper itself

Abstract

backgroundFunctional gastrointestinal disorders (FGIDs), including functional dyspepsia (FD) and irritable bowel syndrome (IBS), are characterized by chronic and recurrent gastrointestinal symptoms. Clinically, FD and IBS often resemble gastrointestinal dysmotility caused by autoimmune autonomic neuropathy. We examined the seropositive frequency of autoantibodies against ganglionic nicotinic acetylcholine receptors (gnAChRs) in patients presenting with FGIDs.

objectiveTo elucidate the seropositivity of gnAChR antibodies and the clinical features of seropositive FD and IBS. MATERIALS AND

methodsWe measured autoantibodies against the gnAChR α3 and β4subunits using luciferase immunoprecipitation systems. Serum samples from patients with any autonomic symptoms were obtained from hospitals in Japan between January 2012 and August 2018 (1787 serum samples of 1381 patients). We selected FD and IBS patients and compared the clinical characteristics and prevalence of autonomic symptoms between those with seropositive and seronegative IBS and FD.

resultsNine IBS and two FD cases (one comorbid case with IBS) were found. We found four patients (36.4%) in whom gnAChR antibodies were positive in these eleven patients. Sicca symptoms were observed in three of four cases (75%) of seropositive FGID compared with zero of seven cases (0%) of seronegative FGID.

conclusionsWe found patients with gnAChR antibodies in FD and IBS patients. These data will be valuable for elucidating the pathophysiology of these FGIDs and developing new treatment strategies.

Indexed as

anti-ganglionic acetylcholine receptorautoantibodyfunctional dyspepsiafunctional gastrointestinal disordersirritable bowel syndrome

Identifiers

PMID38793066
PMCPMC11122234

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