The Assessment of the Association of Proton Pump Inhibitor Usage with Chronic Kidney Disease Progression through a Process Mining Approach Show others and affiliations
2024 (English) In: Biomedicines, E-ISSN 2227-9059, Vol. 12, no 6, article id 1362Article in journal (Refereed) Published
Abstract [en]
Previous studies have suggested an association between Proton Pump Inhibitors (PPIs) and the progression of chronic kidney disease (CKD). This study aims to assess the association between PPI use and CKD progression by analysing estimated glomerular filtration rate (eGFR) trajectories using a process mining approach. We conducted a retrospective cohort study from 1 January 2006 to 31 December 2011, utilising data from the Stockholm Creatinine Measurements (SCREAM). New users of PPIs and H2 blockers (H2Bs) with CKD (eGFR < 60) were identified using a new-user and active-comparator design. Process mining discovery is a technique that discovers patterns and sequences in events over time, making it suitable for studying longitudinal eGFR trajectories. We used this technique to construct eGFR trajectory models for both PPI and H2B users. Our analysis indicated that PPI users exhibited more complex and rapidly declining eGFR trajectories compared to H2B users, with a 75% increased risk (adjusted hazard ratio [HR] 1.75, 95% confidence interval [CI] 1.49 to 2.06) of transitioning from moderate eGFR stage (G3) to more severe stages (G4 or G5). These findings suggest that PPI use is associated with an increased risk of CKD progression, demonstrating the utility of process mining for longitudinal analysis in epidemiology, leading to an improved understanding of disease progression.
Place, publisher, year, edition, pages MDPI AG , 2024. Vol. 12, no 6, article id 1362
Keywords [en]
eGFR trajectory, process mining, multistate model, proton pump inhibitors (PPIs), H2 blockers (H2Bs), chronic kidney disease (CKD), longitudinal data analysis
National Category
Clinical Medicine
Identifiers URN: urn:nbn:se:hb:diva-33185 DOI: 10.3390/biomedicines12061362 ISI: 001254956100001 PubMedID: 38927569 Scopus ID: 2-s2.0-85197854409 OAI: oai:DiVA.org:hb-33185 DiVA, id: diva2:1929814
2024-07-082025-01-212025-01-21 Bibliographically approved