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Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis

OBJECTIVE: To estimate the association between the use of sodium glucose co-transporter-2 (SGLT2) inhibitors and postmarket harms as identified by drug regulatory agencies. DESIGN: We conducted a systematic review and meta-analysis of randomised controlled trials (RCT). Six large databases were sear...

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Autores principales: Donnan, Jennifer R, Grandy, Catherine A, Chibrikov, Eugene, Marra, Carlo A, Aubrey-Bassler, Kris, Johnston, Karissa, Swab, Michelle, Hache, Jenna, Curnew, Daniel, Nguyen, Hai, Gamble, John-Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361337/
https://www.ncbi.nlm.nih.gov/pubmed/30813108
http://dx.doi.org/10.1136/bmjopen-2018-022577
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author Donnan, Jennifer R
Grandy, Catherine A
Chibrikov, Eugene
Marra, Carlo A
Aubrey-Bassler, Kris
Johnston, Karissa
Swab, Michelle
Hache, Jenna
Curnew, Daniel
Nguyen, Hai
Gamble, John-Michael
author_facet Donnan, Jennifer R
Grandy, Catherine A
Chibrikov, Eugene
Marra, Carlo A
Aubrey-Bassler, Kris
Johnston, Karissa
Swab, Michelle
Hache, Jenna
Curnew, Daniel
Nguyen, Hai
Gamble, John-Michael
author_sort Donnan, Jennifer R
collection PubMed
description OBJECTIVE: To estimate the association between the use of sodium glucose co-transporter-2 (SGLT2) inhibitors and postmarket harms as identified by drug regulatory agencies. DESIGN: We conducted a systematic review and meta-analysis of randomised controlled trials (RCT). Six large databases were searched from inception to May 2018. Random effects models were used to estimate pooled relative risks (RRs). INTERVENTION: SGLT2 inhibitors, compared with placebo or active comparators. PRIMARY OUTCOMES: Acute kidney injury (AKI), diabetic ketoacidosis (DKA), urinary tract infections (UTI), bone fractures and lower limb amputations. RESULTS: We screened 2418 citations of which 109 were included. Most studies included one of four SGLT2 inhibitors, dapagliflozin, canagliflozin, empagliflozin and ipragliflozin. When compared with placebo, SGLT2 inhibitors were found to be significantly protective against AKI (RR=0.59; 95% CI 0.39 to 0.89; I(2)=0.0%), while no difference was found for DKA (RR 0.66; 95% CI 0.30 to 1.45, I(2)=0.0%), UTI (RR 1.02; 95% CI 0.95 to 1.09, I(2)=0.0%) or bone fracture (RR 0.87; 95% CI 0.69 to 1.09, I(2)=1.3%). Three studies reported on amputation, with one finding a significant increase risk. No increased risk for either outcome was found when compared with active controls. Subgroup analysis did show an increased risk of UTI with dapagliflozin only (RR 1.21; 95% CI 1.02 to 1.43, I(2)=0.0%), but no other analysis supported an increased risk of AKI, DKA, UTI or fracture. CONCLUSIONS: Current evidence from RCTs does not suggest an increased risk of harm with SGLT2 inhibitors as a class over placebo or active comparators with respect to AKI, DKA, UTI or fracture. However, wide CIs for many comparisons suggest limited precision, and therefore clinically important adverse events cannot be ruled out. Dapagliflozin, appears to independently increase the risk of UTI, although the mechanism for this intraclass variation in risk is unclear. PROSPERO REGISTRATION NUMBER: CRD42016038715.
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spelling pubmed-63613372019-02-27 Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis Donnan, Jennifer R Grandy, Catherine A Chibrikov, Eugene Marra, Carlo A Aubrey-Bassler, Kris Johnston, Karissa Swab, Michelle Hache, Jenna Curnew, Daniel Nguyen, Hai Gamble, John-Michael BMJ Open Diabetes and Endocrinology OBJECTIVE: To estimate the association between the use of sodium glucose co-transporter-2 (SGLT2) inhibitors and postmarket harms as identified by drug regulatory agencies. DESIGN: We conducted a systematic review and meta-analysis of randomised controlled trials (RCT). Six large databases were searched from inception to May 2018. Random effects models were used to estimate pooled relative risks (RRs). INTERVENTION: SGLT2 inhibitors, compared with placebo or active comparators. PRIMARY OUTCOMES: Acute kidney injury (AKI), diabetic ketoacidosis (DKA), urinary tract infections (UTI), bone fractures and lower limb amputations. RESULTS: We screened 2418 citations of which 109 were included. Most studies included one of four SGLT2 inhibitors, dapagliflozin, canagliflozin, empagliflozin and ipragliflozin. When compared with placebo, SGLT2 inhibitors were found to be significantly protective against AKI (RR=0.59; 95% CI 0.39 to 0.89; I(2)=0.0%), while no difference was found for DKA (RR 0.66; 95% CI 0.30 to 1.45, I(2)=0.0%), UTI (RR 1.02; 95% CI 0.95 to 1.09, I(2)=0.0%) or bone fracture (RR 0.87; 95% CI 0.69 to 1.09, I(2)=1.3%). Three studies reported on amputation, with one finding a significant increase risk. No increased risk for either outcome was found when compared with active controls. Subgroup analysis did show an increased risk of UTI with dapagliflozin only (RR 1.21; 95% CI 1.02 to 1.43, I(2)=0.0%), but no other analysis supported an increased risk of AKI, DKA, UTI or fracture. CONCLUSIONS: Current evidence from RCTs does not suggest an increased risk of harm with SGLT2 inhibitors as a class over placebo or active comparators with respect to AKI, DKA, UTI or fracture. However, wide CIs for many comparisons suggest limited precision, and therefore clinically important adverse events cannot be ruled out. Dapagliflozin, appears to independently increase the risk of UTI, although the mechanism for this intraclass variation in risk is unclear. PROSPERO REGISTRATION NUMBER: CRD42016038715. BMJ Publishing Group 2019-02-01 /pmc/articles/PMC6361337/ /pubmed/30813108 http://dx.doi.org/10.1136/bmjopen-2018-022577 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Diabetes and Endocrinology
Donnan, Jennifer R
Grandy, Catherine A
Chibrikov, Eugene
Marra, Carlo A
Aubrey-Bassler, Kris
Johnston, Karissa
Swab, Michelle
Hache, Jenna
Curnew, Daniel
Nguyen, Hai
Gamble, John-Michael
Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title_full Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title_fullStr Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title_full_unstemmed Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title_short Comparative safety of the sodium glucose co-transporter 2 (SGLT2) inhibitors: a systematic review and meta-analysis
title_sort comparative safety of the sodium glucose co-transporter 2 (sglt2) inhibitors: a systematic review and meta-analysis
topic Diabetes and Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361337/
https://www.ncbi.nlm.nih.gov/pubmed/30813108
http://dx.doi.org/10.1136/bmjopen-2018-022577
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