Comparative Outcomes of Newer Antidiabetic Agents in Preventing Diabetic Nephropathy: A Meta-Analysis

Diabetic nephropathy (DN) is known to be one of the central patients' burdens, contributing to the global development of chronic kidney diseases (CKD) and end-stage renal disease (ESRD). Even after the use of non-specific standards such as RAAS inhibitors, the progression of DN remains a challenging clinical problem. Some of the advanced antidiabetic drugs, SGLT2 inhibitors, GLP-1 receptor agonists (GLP-1 RAs), and DPP-4 inhibitors may improve renal function in addition to controlling hyperglycemia. This meta-analysis will compare the clinical efficacy of these newer antidiabetic agents with regard to attaining these objectives, including eGFR decline rate, albuminuria decrease, and the risk of ESRD. Reviews of eligible studies were obtained from PubMed, Embase, Cochrane Library, and Scopus, using keywords related to trial types, including randomised controlled trials (RCTs), cohort studies and meta-analyses with relation to Renal outcome of SGLT2 inhibitors, GLP-1 receptor agonists and DPP-4 inhibitors. Cohen's d was calculated as the measure of effect size, fixed/random as the method of pooling effect sizes and I² as the measure of heterogeneity. The publication bias was assessed by using a funnel plot and Egger's regression test while the sensitivity analyses were done. SGLT2 inhibitors were also found to have the most substantial nephroprotective benefits, including a reduction of the annual decline of eGFR by 1·4–2·0%, albuminuria by 31–38%, and ESRD risk by 29–34%. A moderate renal benefit was established with GLP-1 receptor agonists inclusive of a decrease in eGFR loss to a range of (-1.2%-1.5%), albuminuria (-24%-28%) and risk of ESRD (-21%- 25%) through anti-inflammatory effects. DPP-4 inhibitors, however, recorded only slight improvement of albuminuria (-9 to -12%) and ESRD (-7 to -10%), making it the worst option for nephroprotection. In line with these findings, this meta-analysis has evidence that SGLT2 inhibitors are superior to other antidiabetic drugs from the renal perspective. Secondly, GLP1-RA and, at last, DPP-4 inhibitors have minimal renal protection. These findings endorse the use of SGLT2 inhibitors to start with for patients having diabetes and CKD, along with GLP-1 receptor agonists, to increase cardiovascular and renal benefits.

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Publication Details

Journal
Fortune Journal of Health Sciences
Published
2025-02-20
DOI
https://doi.org/10.26502/fjhs.262
Primary Topic
Chronic Kidney Disease and Diabetes
Type
article
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article

Comparative Outcomes of Newer Antidiabetic Agents in Preventing Diabetic Nephropathy: A Meta-Analysis

Safa Abdalla, Aisha Alyassi, Dana R.Z Hassouna, A. A. Abdalla et al.
Fortune Journal of Health Sciences
Chronic Kidney Disease and Diabetes
article

Comparative Outcomes of Newer Antidiabetic Agents in Preventing Diabetic Nephropathy: A Meta-Analysis

Safa Abdalla, Aisha Alyassi, Dana R.Z Hassouna, A. A. Abdalla, Sara Ahmed Al Amoodi, Hind Saleh Alhammadi, Asal Ahmed Mohammed Al Azzawi, Qamar mohammed kashmoola, Gana Ali Ahmad Tahmaz, Amna Ahmed Alteneiji, Loujain Hussam Subhi nasralla
article en

Abstract

Diabetic nephropathy (DN) is known to be one of the central patients' burdens, contributing to the global development of chronic kidney diseases (CKD) and end-stage renal disease (ESRD). Even after the use of non-specific standards such as RAAS inhibitors, the progression of DN remains a challenging clinical problem. Some of the advanced antidiabetic drugs, SGLT2 inhibitors, GLP-1 receptor agonists (GLP-1 RAs), and DPP-4 inhibitors may improve renal function in addition to controlling hyperglycemia. This meta-analysis will compare the clinical efficacy of these newer antidiabetic agents with regard to attaining these objectives, including eGFR decline rate, albuminuria decrease, and the risk of ESRD. Reviews of eligible studies were obtained from PubMed, Embase, Cochrane Library, and Scopus, using keywords related to trial types, including randomised controlled trials (RCTs), cohort studies and meta-analyses with relation to Renal outcome of SGLT2 inhibitors, GLP-1 receptor agonists and DPP-4 inhibitors. Cohen's d was calculated as the measure of effect size, fixed/random as the method of pooling effect sizes and I² as the measure of heterogeneity. The publication bias was assessed by using a funnel plot and Egger's regression test while the sensitivity analyses were done. SGLT2 inhibitors were also found to have the most substantial nephroprotective benefits, including a reduction of the annual decline of eGFR by 1·4–2·0%, albuminuria by 31–38%, and ESRD risk by 29–34%. A moderate renal benefit was established with GLP-1 receptor agonists inclusive of a decrease in eGFR loss to a range of (-1.2%-1.5%), albuminuria (-24%-28%) and risk of ESRD (-21%- 25%) through anti-inflammatory effects. DPP-4 inhibitors, however, recorded only slight improvement of albuminuria (-9 to -12%) and ESRD (-7 to -10%), making it the worst option for nephroprotection. In line with these findings, this meta-analysis has evidence that SGLT2 inhibitors are superior to other antidiabetic drugs from the renal perspective. Secondly, GLP1-RA and, at last, DPP-4 inhibitors have minimal renal protection. These findings endorse the use of SGLT2 inhibitors to start with for patients having diabetes and CKD, along with GLP-1 receptor agonists, to increase cardiovascular and renal benefits.

Fortune Journal of Health Sciences
Openalex Percentile: Top 91%
Chronic Kidney Disease and Diabetes
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