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Prescribing of evidence-based diabetes pharmacotherapy in patients with metabolic dysfunction-associated steatohepatitis.
Alexopoulos, Anastasia-Stefania; Parish, Alice; Olsen, Maren; Batch, Bryan C; Moylan, Cynthia; Crowley, Matthew J.
Afiliación
  • Alexopoulos AS; Department of Medicine, Division of Endocrinology, Duke University, Durham, North Carolina, USA asa61@duke.edu.
  • Parish A; Center of Innovation to Accelerate Discover and Practice Transformation (ADAPT), Durham VA Medical Center, Durham, North Carolina, USA.
  • Olsen M; Department of Medicine, Division of Endocrinology, Durham VA Medical Center, Durham, North Carolina, USA.
  • Batch BC; Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
  • Moylan C; Center of Innovation to Accelerate Discover and Practice Transformation (ADAPT), Durham VA Medical Center, Durham, North Carolina, USA.
  • Crowley MJ; Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
BMJ Open Diabetes Res Care ; 11(6)2023 11 29.
Article en En | MEDLINE | ID: mdl-38030391
ABSTRACT

INTRODUCTION:

Metabolic dysfunction-associated steatohepatitis (MASH) is highly prevalent in type 2 diabetes (T2D). Pioglitazone and glucagon-like peptide-1 receptor agonists (GLP-1RA) are medications used in T2D that can resolve MASH and should be considered in all patients with T2D and MASH. We assessed prescription rates of evidence-based T2D pharmacotherapy (EBP) in MASH, and ascertained racial/ethnic disparities in prescribing. RESEARCH DESIGN AND

METHODS:

We conducted a cross-sectional study on patients in Duke University Health System with diagnosis codes for T2D and MASH between January 2019 and January 2021. Only patients with ≥1 primary care or endocrinology encounter were included. The primary outcome was EBP, defined as ≥1 prescription for pioglitazone and/or a GLP-1RA during the study period. A multivariable logistic regression model was used to examine the primary outcome.

RESULTS:

A total of 847 patients with T2D and MASH were identified; mean age was 59.7 (SD 12) years, 61.9% (n=524) were female, and 11.9% (n=101) and 4.6% (n=39) were of Black race and Latino/a/x ethnicity, respectively. EBP was prescribed in 34.8% (n=295). No significant differences were noted in the rates of EBP use across racial/ethnic groups (Latino/a/x vs White patients adjusted OR (aOR) 1.82, 95% CI 0.78 to 4.28; Black vs White patients aOR 0.76, 95% CI 0.44 to 1.33, p=0.20).

CONCLUSIONS:

EBP prescriptions, especially pioglitazone, are low in patients with T2D and MASH, regardless of race/ethnicity. These data underscore the need for interventions to close the gap between current and evidence-based care.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Hígado Graso Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: BMJ Open Diabetes Res Care Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Hígado Graso Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: BMJ Open Diabetes Res Care Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos