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August 4, 2021Diabetes Care56 citationsOpen Access

Second-Line Therapy for Type 2 Diabetes Management: The Treatment/Benefit Paradox of Cardiovascular and Kidney Comorbidities

RMRozalina G. McCoyHHHolly K. Van HoutenPKPinar Karaca‐Mandic

Structured PICO

Are GLP-1RA and SGLT2i preferentially initiated over DPP-4i in type 2 diabetes patients with cardiovascular disease, heart failure, or nephropathy?

P
Population
225,513 adults with type 2 diabetes (commercially insured and Medicare Advantage beneficiaries) who first started GLP-1RA (n=75,395), SGLT2i (n=58,234), or DPP-4i (n=91,884) therapy between 2016 and 2019.
I
Intervention
Initiation of glucagon-like peptide 1 receptor agonists (GLP-1RA) or sodium-glucose cotransporter 2 inhibitors (SGLT2i)
C
Comparator
Initiation of dipeptidyl peptidase 4 inhibitors (DPP-4i)
O
Outcome
Relative risk ratios (RRR) of starting GLP-1RA and SGLT2i compared with DPP-4i for those with a history of myocardial infarction (MI), cerebrovascular disease, heart failure (HF), and nephropathy

Despite established cardiovascular and kidney benefits, patients with type 2 diabetes and these comorbidities are paradoxically less likely to be prescribed GLP-1RA or SGLT2i compared to DPP-4i.

Abstract

OBJECTIVE: To examine whether glucagon-like peptide 1 receptor agonists (GLP-1RA) and sodium-glucose cotransporter 2 inhibitors (SGLT2i) are preferentially initiated among patients with cardiovascular disease, heart failure (HF), or nephropathy, where these drug classes have established benefit, compared with dipeptidyl peptidase 4 inhibitors (DPP-4i), for which corresponding benefits have not been demonstrated. RESEARCH DESIGN AND METHODS: We retrospectively analyzed claims of adults with type 2 diabetes included in OptumLabs Data Warehouse, a deidentified database of commercially insured and Medicare Advantage beneficiaries, who first started GLP-1RA, SGLT2i, or DPP-4i therapy between 2016 and 2019. Using multinomial logistic regression, we examined the relative risk ratios (RRR) of starting GLP-1RA and SGLT2i compared with DPP-4i for those with a history of myocardial infarction (MI), cerebrovascular disease, HF, and nephropathy after adjusting for demographic and other clinical factors. RESULTS: We identified 75,395 patients who started GLP-1RA, 58,234 who started SGLT2i, and 91,884 who started DPP-4i. Patients with prior MI, cerebrovascular disease, or nephropathy were less likely to start GLP-1RA rather than DPP-4i compared with patients without these conditions (RRR 0.83 95% CI 0.78-0.88 for MI, RRR 0.77 0.74-0.81 for cerebrovascular disease, and RRR 0.87 0.84-0.91 for nephropathy). Patients with HF or nephropathy were less likely to start SGLT2i (RRR 0.83 0.80-0.87 for HF and RRR 0.57 0.55-0.60 for nephropathy). Both medication classes were less likely to be started by non-White and older patients. CONCLUSIONS: Patients with cardiovascular disease, HF, and nephropathy, for whom evidence suggests a greater likelihood of benefiting from GLP-1RA and/or SGLT2i therapy, were less likely to start these drugs. Addressing this treatment/benefit paradox, which was most pronounced in non-White and older patients, may help reduce the morbidity associated with these conditions.

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Cite This Study

McCoy et al. (2021) studied this question.

synapsesocial.com/papers/6a03a3d75fd9143e45855eb4https://doi.org/10.2337/dc20-2977
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