Evidence map›Paper›PMID 42321733›Full record

ArticleBMC psychiatry2026

Prevalence and risk factors of bipolar disorder in central nervous system autoimmune demyelinating diseases.

Omid Mirmosayyeb, Sepehr Aghajanian, Saeed Vaheb, Fateme Mohammadifard, Mohammad Reza Sharbafchi, Vahid Shaygannejad

Abstract read
In one paragraph

Article in BMC psychiatry, 2026. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Omid MirmosayyebIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Sepehr AghajanianIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Saeed VahebIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Fateme MohammadifardIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Mohammad Reza SharbafchiBehavioral Sciences Research Center & Department of Psychiatry, Khorshid Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Vahid ShaygannejadIsfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran. v.shaygannejad@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAffective disorders, including bipolar disorder (BPD), are increasingly recognized in patients with multiple sclerosis (pwMS), yet their comparable prevalence across MS subtypes and in neuromyelitis optica spectrum disorder (NMOSD) remains unclear. This study aimed to estimate the prevalence of BPD among patients with MS and NMOSD and to identify clinical and demographic factors associated with increased BPD risk.

methodsWe conducted a cross-sectional study involving 4,460 patients with MS and 299 patients with NMOSD. Psychiatric assessments were performed using structured interviews based on DSM-IV criteria. Demographic, neurological, and treatment data were collected from medical records and clinician evaluations. Multivariate logistic regression was used to assess factors associated with BPD, including disease subtype, disability level (EDSS), and clinical presentation.

resultsThe overall prevalence of BPD was 3.07%, with the highest rate in SPMS (5.63%), followed by NMOSD (4.68%). The risk of BPD was comparable among NMOSD vs. MS patients (OR:1.15; 95%CI:0.60-2.17). Among pwMS, RRMS (2.48%) and PPMS (1.42%) had statistically comparable rates of BPD (OR: 0.55; 95%CI: 0.17-1.76); however, SPMS patients had highest prevalence of BPD that was statistically greater than RRMS (OR: 2.32; 95%CI: 1.57-3.44). Higher EDSS, single relationship status, addiction, smoking, and cerebellar symptoms at onset were also associated with higher likelihood of BPD.

conclusionsHigher disability in SPMS, early cerebellar involvement, and psychosocial factors were associated with higher odds of BPD. These findings underscore the need for routine psychiatric screening and tailored support strategies in high-risk subgroups.

Indexed as

Bipolar DisorderMultiple SclerosisNeuromyelitis OpticaAdultComorbidityCross-Sectional StudiesFemaleHumansMaleMiddle AgedPrevalenceRisk FactorsAffective disorderAquaporin-4Bipolar disorderEpidemiologyMultiple sclerosisNeuromyelitis optica

Identifiers

PMID42321733
PMCPMC13540898

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.