Characteristics of new users of recent antidiabetic drugs in Canada and the United Kingdom.


Journal

BMC endocrine disorders
ISSN: 1472-6823
Titre abrégé: BMC Endocr Disord
Pays: England
ID NLM: 101088676

Informations de publication

Date de publication:
29 Sep 2022
Historique:
received: 14 04 2022
accepted: 01 09 2022
entrez: 29 9 2022
pubmed: 30 9 2022
medline: 4 10 2022
Statut: epublish

Résumé

Characteristics of patients using newer 2 We conducted a multi-database cohort study using administrative health databases from 7 Canadian provinces and the UK Clinical Practice Research Datalink. We assembled a base cohort of antidiabetic drug users between 2006 and 2018, from which we constructed 3 cohorts of new users of SGLT-2i, DPP-4i, and GLP-1 RA between 2016 and 2018. Our cohorts included 194,070 new users of DPP-4i, 166,722 new users of SGLT-2i, and 27,719 new users of GLP-1 RA. New users of GLP-1 RA were more likely to be younger (mean ± SD: 56.7 ± 12.2 years) than new users of DPP-4i (67.8 ± 12.3 years) or SGLT-2i (64.4 ± 11.1 years). In Canada, new users of DPP-4i were more likely to have a history of coronary artery disease (22%) than new users of SGLT-2i (20%) or GLP-1 RA (15%). Although SGLT-2i, DPP-4i, and GLP-1 RAs are recommended as 2

Sections du résumé

BACKGROUND BACKGROUND
Characteristics of patients using newer 2
METHODS METHODS
We conducted a multi-database cohort study using administrative health databases from 7 Canadian provinces and the UK Clinical Practice Research Datalink. We assembled a base cohort of antidiabetic drug users between 2006 and 2018, from which we constructed 3 cohorts of new users of SGLT-2i, DPP-4i, and GLP-1 RA between 2016 and 2018.
RESULTS RESULTS
Our cohorts included 194,070 new users of DPP-4i, 166,722 new users of SGLT-2i, and 27,719 new users of GLP-1 RA. New users of GLP-1 RA were more likely to be younger (mean ± SD: 56.7 ± 12.2 years) than new users of DPP-4i (67.8 ± 12.3 years) or SGLT-2i (64.4 ± 11.1 years). In Canada, new users of DPP-4i were more likely to have a history of coronary artery disease (22%) than new users of SGLT-2i (20%) or GLP-1 RA (15%).
CONCLUSION CONCLUSIONS
Although SGLT-2i, DPP-4i, and GLP-1 RAs are recommended as 2

Identifiants

pubmed: 36175881
doi: 10.1186/s12902-022-01140-1
pii: 10.1186/s12902-022-01140-1
pmc: PMC9520836
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Glucagon-Like Peptide-1 Receptor 0
Hypoglycemic Agents 0
Sodium-Glucose Transporter 2 Inhibitors 0
Symporters 0
Glucagon-Like Peptide 1 89750-14-1
Sodium 9NEZ333N27
Dipeptidyl-Peptidases and Tripeptidyl-Peptidases EC 3.4.14.-
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

241

Investigateurs

Samy Suissa (S)
Colin R Dormuth (CR)
Brenda R Hemmelgarn (BR)
Jacqueline Quail (J)
Dan Chateau (D)
J Michael Paterson (JM)
Jacques LeLorier (J)
Adrian R Levy (AR)
Pierre Ernst (P)
Kristian B Filion (KB)
Robert W Platt (RW)
Ingrid S Sketris (IS)

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Vanessa C Brunetti (VC)

Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Quebec, Canada.
Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada.

Audray St-Jean (A)

Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada.

Sophie Dell'Aniello (S)

Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada.

Anat Fisher (A)

Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.

Oriana H Y Yu (OHY)

Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada.
Division of Endocrinology, Department of Medicine, Jewish General Hospital, Quebec, Montreal, Canada.

Shawn C Bugden (SC)

College of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
School of Pharmacy, Memorial University of Newfoundland, St John's, Newfoundland and Labrador, Canada.

Jean-Marc Daigle (JM)

Institut national d'excellence en santé et en services sociaux (INESSS), Quebec, Quebec, Canada.

Nianping Hu (N)

The Health Quality Council, Saskatoon, Saskatchewan, Canada.

Silvia Alessi-Severini (S)

College of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Manitoba Centre for Health Policy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.

Baiju R Shah (BR)

ICES, Toronto, Ontario, Canada.
Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Paul E Ronksley (PE)

Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

Lisa M Lix (LM)

Department of Community Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.

Pierre Ernst (P)

Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada.
Department of Medicine, McGill University, Quebec, Montreal, Canada.

Kristian B Filion (KB)

Department of Epidemiology, Biostatistics, and Occupational Health, McGill University, Montreal, Quebec, Canada. kristian.filion@mcgill.ca.
Center for Clinical Epidemiology, Lady Davis Institute, Jewish General Hospital, 3755 Côte Ste Catherine, Suite H410.1, Montreal, Quebec, H3T 1E2, Canada. kristian.filion@mcgill.ca.
Department of Medicine, McGill University, Quebec, Montreal, Canada. kristian.filion@mcgill.ca.

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Classifications MeSH