Evidence map›Paper›PMID 42086258›Full record

Observational studyBMJ open2026

Systemic inflammation and malaria co-infection in irritable bowel syndrome: a cross-sectional study of 142 Yemeni patients.

Naif Taleb Ali, Mansour Abdulnabi H Mehdi, Radfan Saleh Abdullah, Ali N M Gubran, Nazeh Mohammed Al-Abd, Gamila Saleh Ali, Hana Mohsen Ali

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in BMJ open, 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

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Naif Taleb AliDepartment of Medical Laboratory, University of Lahej Radfan University College, Al Habilayn, Yemen N.taleb@ust.edu.ORCID http://orcid.org/0000-0002-2266-1569
Mansour Abdulnabi H MehdiDepartment of Medical Laboratory, University of Lahej Radfan University College, Al Habilayn, Yemen.
Radfan Saleh AbdullahDepartment of Medical Laboratory, University of Lahej Radfan University College, Al Habilayn, Yemen.
Ali N M GubranDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Science and Technology, Aden, Yemen.
Nazeh Mohammed Al-AbdDepartment of Health Sciences, Faculty of Medicine and Health Sciences, University of Science and Technology, Aden, Yemen.
Gamila Saleh AliDepartment of Medicine, University of Aden Faculty of Medicine and Health Science, Aden, Yemen.ORCID http://orcid.org/0009-0005-5504-1920
Hana Mohsen AliDepartment of Medicine, University of Aden Faculty of Medicine and Health Science, Aden, Yemen.ORCID http://orcid.org/0009-0005-6144-4769

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the prevalence of malaria co-infection among patients with irritable bowel syndrome (IBS) in Yemen and to evaluate the association of systemic inflammatory biomarkers (neutrophil-to-lymphocyte ratio (NLR), mean platelet volume (MPV) and platelet-to-lymphocyte ratio (PLR)) with this co-infection.

designMulticentre, cross-sectional observational study conducted between April and December 2024.

settingPrimary and secondary healthcare facilities across 21 governorates in Yemen.

participants142 consecutive adult patients (aged 18-70 years) diagnosed with IBS according to the Rome IV criteria. OUTCOME MEASURES: The primary outcome was the prevalence of malaria infection, confirmed by a rapid diagnostic test . Secondary outcomes included differences in NLR, MPV and PLR between groups, assessed using independent t-tests, and the diagnostic performance of these biomarkers evaluated by receiver operating characteristic curve analysis with AUC calculation. Multivariate binary logistic regression was used to identify independent predictors of malaria co-infection, adjusting for potential confounders.

resultsThe mean age was 42.3 years (SD 11.7) with an equal gender distribution. The prevalence of malaria co-infection was 45.1% (64/142). Patients with malaria positivity had significantly higher NLR (mean difference 0.56, 95% CI 0.40 to 0.72; p<0.001) and PLR (mean difference 22.6, 95% CI 17.8 to 27.4; p<0.001) and lower MPV (mean difference -0.60 fL, 95% CI -0.77 to -0.43; p<0.001) compared with malaria-negative patients. In adjusted logistic regression, higher NLR (adjusted OR 3.21, 95% CI 1.89 to 5.45) and PLR (adjusted OR per 10-unit increase 4.02, 95% CI 2.24 to 7.18) were independently associated with malaria positivity.

conclusionsNearly half of the Yemeni patients with IBS in this study had malaria co-infection, with the highest burden in diarrhoea-predominant and mixed subtypes. Elevated NLR and PLR were strongly associated with co-infection, suggesting these readily available biomarkers could aid targeted screening in resource-limited, endemic settings.

Indexed as

CoinfectionInflammationIrritable Bowel SyndromeMalariaAdolescentAdultAgedBiomarkersCross-Sectional StudiesFemaleHumansMaleMean Platelet VolumeMiddle AgedNeutrophilsPrevalenceBiomarkersInflammationIrritable Bowel SyndromeMalaria

Identifiers

PMID42086258
PMCPMC13150899

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Registered trials

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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.