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Sex disparities in receiving evidence-based medications in patients with CKD
Rui Du1,2, Hannah Wallace2, Jeffrey T Ha2,3
1School of Basic Medical Science, Tsinghua Medicine, Tsinghua University, Beijing, China.
Insights
Female patients with chronic kidney disease (CKD) receive evidence-based medications like renin-angiotensin system inhibitors (RASi) and sodium glucose co-transporter 2 inhibitors (SGLT2i) less often than males. These disparities persist regardless of risk factors, suggesting potential global treatment inequities.
Area of Science:
- Nephrology
- Public Health
- Health Equity
Background:
- Chronic kidney disease (CKD) presents a significant and increasing global health challenge.
- Existing research indicates sex disparities in CKD prevalence and patient outcomes.
- However, comprehensive data on sex-based differences in the therapeutic management of CKD is limited.
Purpose of the Study:
- To investigate and quantify sex disparities in the utilization of evidence-based medications among a diverse global cohort of patients with CKD.
- To identify if these disparities are influenced by key clinical characteristics such as age, disease severity, and comorbidities.
Main Methods:
- Analysis of a prospective, observational, international cohort (Global Kidney Patient Trials Network - GKPTN) of CKD patients.
- Primary exposure: biological sex. Primary outcomes: receipt of renin-angiotensin system inhibitors (RASi), sodium glucose co-transporter 2 inhibitors (SGLT2i), and diuretics.
- Adjusted multivariable logistic regression models were employed to assess the association between sex and medication receipt, controlling for covariates and examining interactions with clinical factors.
Main Results:
- The study included 4192 participants, with females comprising 40.9%.
- Females demonstrated significantly lower odds of receiving RASi (OR=0.75, P<0.001) and SGLT2i (OR=0.79, P=0.03) compared to males, even after multivariable adjustment.
- No significant sex difference was observed in the receipt of diuretics, and no significant interactions were found between sex and other clinical characteristics.
Conclusions:
- Female CKD patients are less likely to be prescribed guideline-recommended medications, specifically RASi and SGLT2i, compared to their male counterparts.
- These observed sex-based disparities in medication use are consistent across various risk profiles and may contribute to differential health outcomes.
- The findings underscore the need to address potential inequities in CKD treatment globally to improve patient care and outcomes.
Background And Hypothesis:
Chronic kidney disease (CKD) is a growing global health burden. While studies have demonstrated sex disparities in CKD prevalence and outcomes, evidence on sex-based differences in therapeutic management remains limited. This analysis aims to assess sex disparities in the receipt of evidence-based medications in a global CKD cohort.
Methods:
This study is a sub-study of the Global Kidney Patient Trials Network (GKPTN), a prospective, observational, international cohort of CKD patients. The exposure of this study is biological sex, and the main outcomes are the receipt of evidence-based medications for CKD, including renin-angiotensin system inhibitors (RASi), sodium glucose co-transporter 2 inhibitor (SGLT2i) and diuretics. Adjusted multivariable logistic models were conducted to examine associations between sex and proportion of receiving medications, as well as the interactions between sex and other key clinical characteristics (advanced age, high KDIGO prognosis risk, and comorbid condition).
Results:
A total of 4192 participants were eligible, and 40.9% were female. Females had lower odds of receiving RASi (OR = 0.75, 95% CI 0.64-0.88; P < 0.001) and SGLT2i (OR = 0.79, 95% CI 0.64-0.98; P = 0.03) compared to males, after adjusting for age, region, systolic blood pressure (SBP), body mass index (BMI), presence of cardiovascular disease and diabetes, CKD aetiology and prognosis risk, with no significant difference in the receipt of diuretics. There were no significant interactions between sex and any other key clinical characteristics, indicating that the disparities in the receipt of RASi and SGLT2i remained consistent across high-risk subgroups.
Conclusion:
Female patients with CKD are less likely to receive evidence-based medications than males, irrespective of established CKD risk factors. This difference highlights potential inequities in treatment globally which may result in outcome disparities.
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