Evidence map›Paper›PMID 32967856›Full record

Observational studyBMJ (Clinical research ed.)2020

Sodium glucose cotransporter 2 inhibitors and risk of major adverse cardiovascular events: multi-database retrospective cohort study.

Kristian B Filion, Lisa M Lix, Oriana Hy Yu, Sophie Dell'Aniello, Antonios Douros, Baiju R Shah, Audray St-Jean, Anat Fisher, Eric Tremblay, Shawn C Bugden and 7 more

Registry-linked trialOpen access · hybridAbstract readObservational Study
In one paragraph

Observational study in BMJ (Clinical research ed.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT03939624. Cited by 63 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 4 pooled it
11.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03939624 completed

Sodium-glucose Cotransporter 2 (SGLT2) Inhibitors and the Risk of Cardiovascular Events Among Patients With Type 2 Diabetes: a Multicenter Cohort Study

Ran2018Enrolled419,734Registered outcomes5Posted comparisons0ConditionsAll-Cause Mortality, Cardiovascular Death, Heart Failure, Ischemic StrokeArmsDipeptidyl Peptidase-4 (DPP-4) Inhibitors, Sodium-glucose cotransporter 2 (SGLT2) inhibitors
PMID 36175881PMID 34332563PMID 27610604other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 4 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 9 institutions in 2 countries.

Kristian B FilionCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada kristian.filion@mcgill.ca.ORCID 0000-0001-6055-0088
Lisa M LixDepartment of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Oriana Hy YuCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Sophie Dell'AnielloCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Antonios DourosCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Baiju R ShahICES, Toronto, Ontario, Canada.
Audray St-JeanCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Anat FisherDepartment of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, Canada.
Eric TremblayInstitut national d'excellence en santé et en services sociaux (INESSS), Quebec City, Quebec, Canada.
Shawn C BugdenCollege of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Silvia Alessi-SeveriniCollege of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Paul E RonksleyDepartment of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Nianping HuThe Health Quality Council, Saskatoon, Saskatchewan, Canada.
Colin R DormuthDepartment of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, Canada.
Pierre ErnstCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Samy SuissaCentre for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Cote Ste-Catherine Road, Suite H485, Montreal, Quebec, Canada.
Canadian Network for Observational Drug Effect Studies (CNODES) Investigators
Jewish General Hospital · CAUniversity of British Columbia · CAInstitut National d'Excellence en Santé et en Services Sociaux · CAManitoba Health · CAMemorial University of Newfoundland · CASaskatchewan Health Quality Council · CASunnybrook Health Science Centre · CAUniversity of Calgary · CAUniversity of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare the risk of cardiovascular events between sodium glucose cotransporter 2 (SGLT2) inhibitors and dipeptidyl peptidase-4 (DPP-4) inhibitors among people with type 2 diabetes in a real world context of clinical practice.

designMulti-database retrospective cohort study using a prevalent new user design with subsequent meta-analysis.

settingCanadian Network for Observational Drug Effect Studies (CNODES), with administrative healthcare databases from seven Canadian provinces and the United Kingdom, 2013-18. POPULATION: 209 867 new users of a SGLT2 inhibitor matched to 209 867 users of a DPP-4 inhibitor on time conditional propensity score and followed for a mean of 0.9 years.

main outcome measuresThe primary outcome was major adverse cardiovascular events (MACE, a composite of myocardial infarction, ischaemic stroke, or cardiovascular death). Secondary outcomes were the individual components of MACE, heart failure, and all cause mortality. Cox proportional hazards models were used to estimate site specific adjusted hazards ratios and 95% confidence intervals, comparing use of SGLT2 inhibitors with use of DPP-4 inhibitors in an as treated approach. Site specific results were pooled using random effects meta-analysis.

resultsCompared with DPP-4 inhibitors, SGLT2 inhibitors were associated with decreased risks of MACE (incidence rate per 1000 person years: 11.4

conclusionsIn this large observational study conducted in a real world clinical practice context, the short term use of SGLT2 inhibitors was associated with a decreased risk of cardiovascular events compared with the use of DPP-4 inhibitors.

trial registrationClinicalTrials.gov NCT03939624.

Indexed as

AdolescentAdultAgedAged, 80 and overCanadaCardiovascular DiseasesDatabases, FactualDiabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsFemaleHumansIncidenceMaleMiddle AgedRetrospective StudiesSodium-Glucose Transporter 2 InhibitorsDipeptidyl-Peptidase IV InhibitorsSodium-Glucose Transporter 2 Inhibitors

Identifiers

PMID32967856
PMCPMC8009082
OpenAlexW3088446089

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.