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Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps.

Publication ,  Journal Article
LeBlanc, ES; Brooks, N; Davies, M; Chatterjee, R
Published in: J Clin Endocrinol Metab
November 18, 2024

PURPOSE: There are large disparities in the impact of diabetes on cardiovascular disease (CVD) risk and outcomes by sex and gender. Achieving health equity requires understanding risks and medication efficacy in female patients, especially now, as novel pharmacologic treatments are transforming the diabetes and CVD treatment landscape. This review examines 2 bodies of research that can inform sex differences in CVD in patients with diabetes: female-specific risk factors for CVD and sex-related limitations of clinical trial research in evaluating novel diabetes and CVD treatments. METHODS: Two literature searches were performed using Ovid Medline(R) All. The first retrieved manuscripts covering sex and gender differences related to CVD risk and therapies and diabetes. The second focused on randomized controlled trial data on sex/gender differences and GLP-1/SGLT-2/DPP-4 drugs. RESULTS: Female-specific risk factors for CVD include early menarche, premature or early menopause, irregular cycles and polycystic ovary syndrome; pregnancy; adverse pregnancy outcomes; history of breast cancer; and autoimmune diseases. Clinical trials of novel pharmacological treatments for diabetes and CVD have undersampled female populations, and clinical characteristics of male and female participants have differed significantly. Thus, evidence to evaluate potential sex differences in treatment efficacy and side effects has been lacking. CONCLUSION: To improve health of female patients with diabetes, sex-specific cardiovascular risk factors should be taken into account in screening and treatment decisions. Further, studies of cardiovascular and diabetes medications must ensure adequate representation by sex and report participant characteristics and outcomes by sex.

Duke Scholars

Published In

J Clin Endocrinol Metab

DOI

EISSN

1945-7197

Publication Date

November 18, 2024

Volume

109

Issue

12

Start / End Page

e2167 / e2177

Location

United States

Related Subject Headings

  • Sex Factors
  • Sex Characteristics
  • Risk Factors
  • Pregnancy
  • Male
  • Hypoglycemic Agents
  • Humans
  • Heart Disease Risk Factors
  • Female
  • Endocrinology & Metabolism
 

Citation

APA
Chicago
ICMJE
MLA
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LeBlanc, E. S., Brooks, N., Davies, M., & Chatterjee, R. (2024). Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps. J Clin Endocrinol Metab, 109(12), e2167–e2177. https://doi.org/10.1210/clinem/dgae655
LeBlanc, Erin S., Neon Brooks, Melinda Davies, and Ranee Chatterjee. “Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps.J Clin Endocrinol Metab 109, no. 12 (November 18, 2024): e2167–77. https://doi.org/10.1210/clinem/dgae655.
LeBlanc ES, Brooks N, Davies M, Chatterjee R. Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps. J Clin Endocrinol Metab. 2024 Nov 18;109(12):e2167–77.
LeBlanc, Erin S., et al. “Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps.J Clin Endocrinol Metab, vol. 109, no. 12, Nov. 2024, pp. e2167–77. Pubmed, doi:10.1210/clinem/dgae655.
LeBlanc ES, Brooks N, Davies M, Chatterjee R. Sex-Specific Cardiovascular Risk Factors and Treatment in Females With T2DM and CVD: Developments and Knowledge Gaps. J Clin Endocrinol Metab. 2024 Nov 18;109(12):e2167–e2177.
Journal cover image

Published In

J Clin Endocrinol Metab

DOI

EISSN

1945-7197

Publication Date

November 18, 2024

Volume

109

Issue

12

Start / End Page

e2167 / e2177

Location

United States

Related Subject Headings

  • Sex Factors
  • Sex Characteristics
  • Risk Factors
  • Pregnancy
  • Male
  • Hypoglycemic Agents
  • Humans
  • Heart Disease Risk Factors
  • Female
  • Endocrinology & Metabolism