Associations between sodium-glucose co-transporter 2 (SGLT-2) inhibitors and urologic diseases: implications for lower urinary tract symptoms from a multi-state health system analysis.


Journal

Urology
ISSN: 1527-9995
Titre abrégé: Urology
Pays: United States
ID NLM: 0366151

Informations de publication

Date de publication:
20 Jun 2024
Historique:
received: 13 03 2024
revised: 28 05 2024
accepted: 14 06 2024
medline: 23 6 2024
pubmed: 23 6 2024
entrez: 22 6 2024
Statut: aheadofprint

Résumé

To analyze the frequency of new urologic visits and urologic diagnoses in patients prescribed sodium-glucose co-transporter-2 inhibitors (SGLT-2is). Records from a multi-state health system between 2014 and 2022 were reviewed to identify patients referred for outpatient urology evaluation within 2 years of diabetes medication prescription. Patients were stratified by the prescription of SGLT-2is or another diabetes medication. Frequency of urology visits within 1-year, urologic diagnoses, and prescriptions to treat lower urinary tract symptoms (LUTS) were compared. Patients were stratified by whether they had achieved HbA1c goal (≥7% or <7%) following treatment as well as by sex. Multivariable logistic regression was performed to determine if SGLT-2 use independently predicted outcomes of interest. 163,827 patients met inclusion criteria. Use of SGLT-2is was associated with a higher frequency of early urologic referral, balanitis/balanoposthitis, overactive bladder, urinary frequency, urgency, and need for LUTS medications in males with HbA1c ≥7%. Females on SGLT-2is with HbA1c ≥7% also had higher rates of urinary incontinence. In those with HbA1c <7%, only balanitis/balanoposthitis and urinary incontinence were higher in the SGLT-2i cohorts for males and females, respectively. Multivariable analysis found SGLT-2i use as predictive of early urology referral, balanitis/balanoposthitis, urinary urgency, frequency, overactive bladder, and need for LUTS medications in males. Multivariable analysis of females demonstrated similar results. SGLT-2is may lead to worse urologic outcomes and increased utilization of urologic care relative to other diabetic medications. Future studies are necessary to identify which patients are at highest risk of adverse urologic outcomes.

Identifiants

pubmed: 38908564
pii: S0090-4295(24)00482-5
doi: 10.1016/j.urology.2024.06.036
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of Competing Interest 1) Bradley Roth- No conflict 2) Bradley Gill- consultant for Boston scientific and Sumitomo Pharma America 3) Prajit Khooblall-No conflict 4) Sanjay Vallabhaneni- No conflict 5) Raevto Bole- No conflict 6) Petar Bajic- consultant for Coloplast Corporation and Boston Scientific

Auteurs

Bradley J Roth (BJ)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH; University of California, Irvine, School of Medicine, Irvine CA. Electronic address: rothbj@hs.uci.edu.

Bradley C Gill (BC)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH. Electronic address: gillb@ccf.org.

Prajit Khooblall (P)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH. Electronic address: khooblp2@ccf.org.

Sanjay Vallabhaneni (S)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH; Northeast Ohio Medical University College of Medicine, Rootstown OH. Electronic address: vallabs4@ccf.org.

Raevti Bole (R)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH. Electronic address: boler@ccf.org.

Petar Bajic (P)

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland OH. Electronic address: bajicp@ccf.org.

Classifications MeSH