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Comparing measured and reported change in gastrointestinal symptoms after initiation of metformin treatment: a questionnaire validation study
Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden; Primary Healthcare Center Cityhälsan Centrum, Region Östergötland, Norrköping, Sweden.
Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden; Department of Women’s and Children’s Health, Karolinska Institutet, Stockholm, Sweden.
School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
School of Medical Sciences, University Health Care Research Centre, Örebro University, Örebro, Sweden and Department of Public Health and Caring Sciences, Uppsala University, Uppsala, Sweden.
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2026 (Engelska)Ingår i: Scandinavian Journal of Primary Health Care, ISSN 0281-3432, E-ISSN 1502-7724, Vol. 44, nr 1, s. 1-9Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Background: The majority of individuals in Sweden with type 2 diabetes have their sole health care provider in primary health care. Metformin treatment often causes gastrointestinal side-effects. Our aim was to construct and validate a questionnaire assessing gastrointestinal symptoms before and after starting metformin treatment for type 2 diabetes.

Methods: In the Interaction Between Metformin and Microbiota (MEMO) study, 54 participants rated six gastrointestinal symptoms at baseline and after 2 months of metformin treatment in a questionnaire (measured change, i.e. the difference between assessments at these two time points), as well as direct assessment of perceived change in symptoms after 2 months in a separate validation questionnaire (reported change, i.e. how participants themselves have perceived the change between the same two time points). Spearman’s ρ was calculated and reported with its 95% CI.

Results: The agreement between reported and measured change of symptoms, measured as Spearman’s ρ, was above 0.4 for 4 out of 6 symptoms (poor appetite 0.60 [95% CI 0.39–0.75], loose stool or diarrhea 0.58 [95% CI 0.37–0.74], flatulence 0.45 [95% CI 0.21–0.64], and abdominal pain 0.45 [95% CI 0.20–0.65]). The agreement was lower for nausea and vomiting, although these were numerically above 75% in agreement, likely due to few symptomatic participants overall.

Conclusion: For common side-effect symptoms associated with metformin treatment, our study shows that symptom change measured as the difference between assessments at two different time-points was in overall agreement, validating the usability of the constructed questionnaire for metformin side-effects.

Ort, förlag, år, upplaga, sidor
Taylor & Francis Group, 2026. Vol. 44, nr 1, s. 1-9
Nyckelord [en]
bowel symptoms, metformin, patient-reported outcome measure (PROM), primary health care, questionnaire, Treatment side-effects
Nationell ämneskategori
Endokrinologi och diabetes
Identifikatorer
URN: urn:nbn:se:umu:diva-247337DOI: 10.1080/02813432.2025.2592696ISI: 001622179700001PubMedID: 41283789Scopus ID: 2-s2.0-105022896396OAI: oai:DiVA.org:umu-247337DiVA, id: diva2:2025839
Tillgänglig från: 2026-01-08 Skapad: 2026-01-08 Senast uppdaterad: 2026-05-20Bibliografiskt granskad

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Kalin, KennyRolandsson, Olov

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