Evidence mapPaperPMID 41285894Full record

ArticleScientific reports2025

Associations of oral hypoglycemic use, fruit intake, and diabetes duration with gastrointestinal autonomic dysfunction in type 2 diabetes patients in Zanzibar.

Hassan Thabit Haji, Ashabilan Ebrahim, Ahmed Gharib Khamis, Ramla Muhidin Ali, Kaushik Ramaiya, Fredirick L Mashili

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

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Hassan Thabit HajiDepartment of Physiology, Muhimbili University of Health and Allied Sciences, Dar-es-salaam, Tanzania. hastha70@gmail.com.
Ashabilan EbrahimDepartment of Physiology, Muhimbili University of Health and Allied Sciences, Dar-es-salaam, Tanzania.
Ahmed Gharib KhamisZanzibar Agricultural and Livestock Research Institute, Zanzibar, Tanzania.
Ramla Muhidin AliSchool of Nursing and Midwifery, Aga Khan University, Dar-es-salaam, Tanzania.
Kaushik RamaiyaDepartment of Medicine, Shree Hindu Mandal Hospital, Dar-es-salaam, Tanzania.
Fredirick L MashiliDepartment of Physiology, Muhimbili University of Health and Allied Sciences, Dar-es-salaam, Tanzania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Gastrointestinal autonomic dysfunction (GAD) is a common complication of Type 2 Diabetes Mellitus (T2DM) leading to gastroparesis, constipation, and gastroesophageal reflux disease, consequently affecting the overall quality of life. However, its prevalence and risk factors remain underexplored, particularly in low-resource settings like Zanzibar. This study assessed the prevalence of GAD and its associations with pharmacological, clinical, and lifestyle factors among T2DM patients in Zanzibar using the Composite Autonomic Symptom Score (COMPASS 31) questionnaire. Methods A cross-sectional study was conducted among 364 T2DM patients attending clinics in Zanzibar. Participants were recruited from local healthcare facilities, and data were collected through structured interviews. The gastrointestinal subdomain of the COMPASS 31 questionnaire quantified symptoms of gastrointestinal dysfunction. Descriptive and inferential analyses were performed to explore prevalence and associated factors. Results Among 364 participants, 140 (38.4%) had GAD. Longer diabetes duration was significantly associated with GAD, with those having diabetes for 7-9 years (adjusted OR: 2.19, p = 0.050) and > 10 years (adjusted OR: 2.04, p = 0.036) at higher risk. Use of oral hypoglycemic agents, more common in those with shorter disease duration, was linked to significantly lower odds of GAD (adjusted OR: 0.43, p = 0.007) compared to insulin alone. Additionally, consuming > 2 portions of fruit per day was associated with reduced risk (adjusted OR: 0.41, p = 0.019). Other factors, including gender and BMI, showed trends but were not statistically significant. Conclusion GAD is common among T2DM patients in Zanzibar, with longer diabetes duration increasing risk, while oral hypoglycemic use and higher fruit intake are linked to lower risk. The protective association of oral hypoglycemics may reflect earlier disease stages, reinforcing the importance of early diagnosis and intervention. Findings highlight the need for integrated lifestyle and pharmacological approaches to mitigate autonomic complications. Future research, including longitudinal studies and clinical trials, should explore causal relationships, underlying mechanisms, and the impact of dietary modifications and pharmacological interventions on GAD.

Indexed as

Autonomic Nervous System DiseasesDiabetes Mellitus, Type 2FruitGastrointestinal DiseasesHypoglycemic AgentsAdministration, OralAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedPrevalenceRisk FactorsSurveys and QuestionnairesHypoglycemic AgentsGastrointestinal autonomic dysfunctionGastrointestinal autonomic neuropathyPrevalenceRisk factorsType 2 diabetes mellitusZanzibar

Identifiers

PMID41285894
PMCPMC12645025

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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 Socratic graph.