<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kanbay M</submitter><funding>Travere Therapeutics</funding><funding>NCATS NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>Doris Duke Charitable Foundation</funding><funding>Steno Diabetes Center Copenhagen (SDCC)</funding><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>Bayer</funding><funding>National Institutes of Health</funding><funding>Centers for Disease Control</funding><funding>NIH HHS</funding><pagination>671-678</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11997758</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Sodium-glucose co-transporter 2 (SGLT2) inhibitors are novel anti-diabetic medications with potential beneficial effects on cardiovascular and renal outcomes, metabolic parameters and body weight. In addition to the beneficial effects on renal function, including estimated glomerular filtration rate and reduction in proteinuria, recent studies have investigated the potential role of SGLT2 inhibitor (SGLT2i) therapy on nephrolithiasis development. Nephrolithiasis, a condition affecting almost 10% of the general population at least once during a lifetime, is a common disorder with considerable risk for acute and chronic kidney injury and relatively few effective therapeutic options.&lt;h4>Methods&lt;/h4>We performed a literature search through multiple databases, including PubMe</pubmed_abstract><journal>Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association</journal><pubmed_title>SGLT2 inhibitors and nephrolithiasis risk: a meta-analysis.</pubmed_title><pmcid>PMC11997758</pmcid><funding_grant_id>U54 DK083912</funding_grant_id><funding_grant_id>OT2HL161847</funding_grant_id><funding_grant_id>75D301-23-C-18264</funding_grant_id><funding_grant_id>U54DK083912</funding_grant_id><funding_grant_id>UL1 TR002319</funding_grant_id><funding_grant_id>U01DK100846</funding_grant_id><funding_grant_id>U01 DK100846</funding_grant_id><funding_grant_id>UM1AI109568</funding_grant_id><funding_grant_id>OT2 OD032581</funding_grant_id><funding_grant_id>R01 MD014712</funding_grant_id><funding_grant_id>U2CDK114886</funding_grant_id><funding_grant_id>SDCC 3.A Complications</funding_grant_id><funding_grant_id>OT2 HL161847</funding_grant_id><funding_grant_id>U24 DK114886</funding_grant_id><funding_grant_id>R01MD014712</funding_grant_id><funding_grant_id>OT2OD032581</funding_grant_id><funding_grant_id>UL1TR002319</funding_grant_id><funding_grant_id>75D301-21-P-12254</funding_grant_id><pubmed_authors>Burlacu A</pubmed_authors><pubmed_authors>Kanbay M</pubmed_authors><pubmed_authors>Rossing P</pubmed_authors><pubmed_authors>Brinza C</pubmed_authors><pubmed_authors>Copur S</pubmed_authors><pubmed_authors>Sekreter O</pubmed_authors><pubmed_authors>Tuttle KR</pubmed_authors><pubmed_authors>Covic A</pubmed_authors></additional><is_claimable>false</is_claimable><name>SGLT2 inhibitors and nephrolithiasis risk: a meta-analysis.</name><description>&lt;h4>Background&lt;/h4>Sodium-glucose co-transporter 2 (SGLT2) inhibitors are novel anti-diabetic medications with potential beneficial effects on cardiovascular and renal outcomes, metabolic parameters and body weight. In addition to the beneficial effects on renal function, including estimated glomerular filtration rate and reduction in proteinuria, recent studies have investigated the potential role of SGLT2 inhibitor (SGLT2i) therapy on nephrolithiasis development. Nephrolithiasis, a condition affecting almost 10% of the general population at least once during a lifetime, is a common disorder with considerable risk for acute and chronic kidney injury and relatively few effective therapeutic options.&lt;h4>Methods&lt;/h4>We performed a literature search through multiple databases, including PubMe</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-04-07T13:20:21.325Z</modification><creation>2026-04-07T13:17:38.148Z</creation></dates><accession>S-EPMC11997758</accession><cross_references><pubmed>39113274</pubmed><doi>10.1093/ndt/gfae179</doi></cross_references></HashMap>