Exp Clin Endocrinol Diabetes 2023; 131(03): 153-161
DOI: 10.1055/a-1927-4454
Article

Do Glucagonlike Peptide-1 Receptor Agonist and Sodium-glucose Co-transporter 2 Inhibitor Prescriptions in Germany Reflect Recommendations for Type 2 Diabetes with Cardiovascular Disease of the ADA/EASD Consensus Report?

Sebastian Dietmar Barth
1   Epidemiology, IQVIA, Frankfurt, Germany
,
Karel Kostev
1   Epidemiology, IQVIA, Frankfurt, Germany
,
Magdalene Krensel
2   Novo Nordisk, Mainz, Germany
,
Elke Mathey
2   Novo Nordisk, Mainz, Germany
,
Wolfgang Rathmann
3   Institute for Biometrics and Epidemiology, German Diabetes Center, Leibniz Center for Diabetes Research at Heinrich Heine University Düsseldorf, Düsseldorf, Germany
› Author Affiliations

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Abstract

Objectives To analyze whether prescription use of GLP-1RA and SGLT2i in individuals with type 2 diabetes with cardiovascular disease (CVD) has increased after the ADA/EASD consensus guidelines (2018) in a German Real-World setting and which clinical characteristics are associated with prescription use of these drugs.

Methods The Disease Analyzer database (IQVIA) comprises a representative panel of 1,373 general practitioners, diabetologists, and cardiologists throughout Germany (01/2015-12/2020: 12.6 million patients). Newly diagnosed type 2 diabetes (n=45,531) was identified by ICD-10 codes (E11). Matching (1:1) on practice specialty, sex, age, and year of diabetes diagnosis was performed for CVD. Logistic regression models were fitted to obtain adjusted odds ratios (OR) for characteristics associated with prescription use (median follow-up: 1.9 years).

Results Overall, 35% of patients (n=16,006) were treated with glucose-lowering drugs during the first year after type 2 diabetes diagnosis (HbA1c≥7.0%: 80%). GLP-1RA (2.4%) and SGLT2i (8.5%) were rarely prescribed. After the consensus, use of GLP-1RA and SGLT2i increased, however, almost independently of pre-existing CVD (12/2019-11/2020 vs. 12/2017-11/2018: yes, no): GLP-1RA: from 5.7 to 9.2%, 5.2 to 7.6%; SGLT2i: from 13.9 to 20.4%, 12.1 to 16.6%. Among cardiovascular risk factors, the largest OR for GLP-1RA was for obesity (4.5; 95%CI: 3.2–6.3). CVD was moderately related with SGLT2i (1.45; 1.32–1.60) and GLP-1RA (1.35; 1.08–1.69) prescriptions. A weak association was observed between SGLT2i and heart failure (1.18; 95%CI: 1.05–1.32).

Conclusion National prescription use of GLP-1RA and SGLT2i did not come close to the recommendation in subjects with CVD issued by the 2018 ADA/EASD consensus.

Supplementary Material



Publication History

Received: 26 April 2022
Received: 08 July 2022

Accepted: 18 August 2022

Accepted Manuscript online:
18 August 2022

Article published online:
15 December 2022

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