Diabetic kidney disease (DKD) is a global health problem and is an important risk factor for kidney failure and cardiovascular (CV) disease (Alicic et al., 2017). Until recently, renin angiotensin-aldosterone system inhibitors (RAASi) were the only available agents with proven renoprotective benefit (Brenner et al., 2001; Lewis et al., 2001). In 2019, sodium glucose co-transporter-2 inhibitors (SGLT-2i) revolutionized the management of DKD with added cardiovascular and renal benefits (Perkovic et al., 2019; Heerspink et al., 2020; The EMPA-KIDNEY Collaborative Group et al., 2023). The last few years have been promising with the discovery of newer therapies in DKD targeting diverse pathophysiologic pathways (Heerspink et al., 2019; Bakris et al., 2020; Perkovic et al., 2024). Despite these existing therapies, there is a substantial residual risk of kidney disease progression (Figure 1).
FIGURE 1
The pathogenesis of DKD, though initiated by a metabolic disturbance is perpetuated by multiple inter-linked pathways involving the hemodynamic, inflammatory, oxidative, and fibrotic systems (Tuttle et al., 2022). This Research Topic aims to understand these complex mechanisms, identify newer therapeutic targets, and test these agents in well designed clinical trials. Eight articles were published in this Research Topic [retrospective studies (2), animal studies (2), meta-analysis (2), clinical trial (1), and in-depth review (1)]. The in-depth review by Zhang et al. summarizes the proposed mechanisms of albuminuria, the current progress, and the future directions of therapeutic avenues in DKD.
Current practice guidelines recommend withholding SGLT-2i during critical illness requiring hospitalization (“sick day rules”) (Watson et al., 2023). However, in a multicenter retrospective cohort study of adults hospitalized with acute heart failure associated AKI, exposure to SGLT-2i during AKI was associated with no difference in time to renal recovery, but a lower 30-day mortality (Aklilu et al., 2023). Whether these findings can be generalized to all other etiologies of AKI is unknown. In this Research Topic, Alcantar-Vallin et al. explore the role of continuing or initiating SGLT-2i during an AKI episode. This was a retrospective cohort study involving 374 patients hospitalized with AKI, of whom 58 received SGLT-2i treatment during the hospitalization. The authors found that SGLT-2i use was not associated with risk of major adverse kidney events but was associated with a reduced risk of mortality (OR 0.08, 95% CI 0.01–0.64).
In the FLOW trial, semaglutide, a glucagon like peptide-1 receptor agonist (GLP-1RA) was shown to decrease clinically relevant kidney outcomes and death from CV causes in patients with type 2 diabetes and CKD (Perkovic et al., 2024). In a post hoc analysis of this trial, the benefits of semaglutide in reducing kidney outcomes were found to be consistent in participants with and without SGLT-2i use (Mann et al., 2024). In this Research Topic Cao et al. carried out a head-to-head comparison of GLP-1RA and SGLT-2i in patients with DKD. This was a randomized, open-label, non-inferiority trial. A total of 106 patients with type 2 diabetes and chronic kidney disease (CKD) were randomized 1:1 to receive either polyethylene glycol loxenatide (PEG-Loxe) 0.2 mg subcutaneous once weekly or dapagliflozin 10 mg orally once daily for 24 weeks. The primary outcome was change in urine albumin creatinine ratio (UACR) from baseline to 24 weeks. The authors showed that following 24 weeks of treatment there was no difference in change in UACR between the two groups (mean intergroup difference 2.6% (95% CI, -5.3 to -10.4%, p=0.336).
Diabetes is a state of oxidative stress and inflammatory burden, which contributes to complications including diabetic nephropathy. The heightened oxidative stress in diabetes is multi-factorial, such as, activation of polyol and hexosamine pathways, accumulation of glycolysis intermediates, activation of protein kinase C, mitochondrial dysfunction, etc., (Jin et al., 2023). There is a strong mutually enhancing interaction between inflammation and oxidative stress. Pro-inflammatory cytokines and chemokines activate reactive oxygen species (ROS) leading to macrophage activation, resulting in more oxidative stress. In return, ROS induce the expression of pro-inflammatory cytokines by activating transcription factors like nuclear factor-kappa B (NF-kB) and activator protein-1 (AP-1) (Caturano et al., 2023). Hence, addressing oxidative stress and inflammation as potential therapeutic targets for DKD has gained greater significance (Winiarska et al., 2021). In recent years, Chinese herbal medicines have been reported to attenuate progression of DKD by their anti-inflammatory and anti-oxidative properties (Zhong et al., 2015). Chen et al. identified 16 potentially renoprotective Chinese herbal medicines for DKD (PRCHMDKD) which were known to target multiple oxidative stress pathways. The authors then retrospectively analyzed the National Health Insurance Database of Taiwan from 2000 to 2017. They identified 43,480 PRCHMDKD users with DKD and 1,442 PRCHMDKD users with advanced DKD who were matched with an equal number of non-users using a nearest neighbour approach. PRCHMDKD use was associated with reduction in adjusted hazard ratios for kidney failure, all-cause-and CV mortality in the overall and advanced DKD population.
Huangkui capsule (HKC) is a traditional Chinese medicine which is currently approved for treatment of CKD in China. It is made from an ethanol extract of Abelmoschus Manihot flowers (Li et al., 2021). In a multicentre, double blind, placebo-controlled randomized clinical trial (RCT) conducted in China, the combination of irbesartan and HKC was found to significantly reduce albuminuria at 24 weeks as compared to irbesartan alone (Zhao et al., 2022). In this Research Topic, Tan et al. conducted a systematic review and meta-analysis of English and Chinese databases, including RCTs comparing HKC combined with RAASi versus RAASi alone in patients with DKD. This meta-analysis included 32 RCTs with a total of 2,881 patients with DKD. The authors showed that the combination of HKC with RAASi was more effective in reducing 24-hour urine protein, urine albumin excretion rate, UACR, serum creatinine, and blood urea nitrogen as compared to RAASi alone.
The primary pharmacologic metabolites in HKC have been identified as total flavonoids of A. Manihot (TFA). However, the mechanism by which these metabolites decrease albuminuria is unknown. Diao et al. carried out a comprehensive analysis of the primary flavonoid metabolites and their fates in db/db mice treated with HKC. A total of 7 flavonoid prototypes and 38 metabolites were identified in the serum, kidney, and urine of db/db mice. The flavonoid metabolite with the highest exposure in serum and kidney samples was quercetin monoglucuronide sulfate.
Ophiocordyceps sinensis (OS), popularly known as caterpillar mushroom is a medicinal fungus found in India and China (Dai et al., 2024). Currently, there are six main OS preparations available as Chinese patent medicine products. Xue et al. conducted an umbrella review of systematic reviews and Bayesian network meta-analysis to study the efficacy and safety of OS preparations combined with RAASi. A total of 157 RCTs involving 13,143 participants were included in the meta-analysis. The authors showed that addition of OS preparations to RAASi was more effective in reducing 24-hour urine protein levels as compared to RAASi alone. Of the 4 preparations studied, Jinshuibao capsules were found to be most effective.
Recent studies have shown that renal tubular injury in DKD is mediated by lipid accumulation via CD-36 and inflammation via NLRP3 inflammasome pathways (Qiu and Tang, 2016; Yang et al., 2017). Astragaloside IV (AS-IV) has been found to effectively suppress oxidative stress and fibrosis through downregulation of CD-36 in glomerular mesangial and myocardial cells. However, the impact of AS-IV on renal tubular injury in DKD rat models is unknown. In this Research Topic, Li et al. showed that administration of AS-IV reduced fasting blood glucose, UACR and 24-hour urine protein excretion in DKD rats. It also mitigated renal tubular injury and supressed expression of CD-36, NLRP3 and other inflammatory biomarkers. In vitro experiments using palmitic acid-induced HK cells also showed decrease in CD-36 expression, lipid accumulation and NLPRP3 activation with AS-IV treatment.
In conclusion, the articles in this Research Topic open out new therapeutic avenues in the management of DKD. With a rise in global prevalence of diabetes, the prevalence of DKD is expected to double over the next 20 years (Chen, 2022). This Research Topic exemplifies the urgent need to conduct more active research in this field targeting multiple pathogenic pathways.
Statements
Author contributions
EE: Conceptualization, Investigation, Project administration, Software, Supervision, Visualization, Writing–original draft, Writing–review and editing. AV: Writing–review and editing. SV: Writing–review and editing. LV: Writing–review and editing. EF: Writing–review and editing. GN: Supervision, Validation, Writing–review and editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Acknowledgments
We thank all the authors of the papers published in this Research Topic for their valuable contributions to this field and the referees for their constructive reviews.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declare that no Generative AI was used in the creation of this manuscript.
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Summary
Keywords
diabetes mellitus, pathomechanisms, oxidative stress, SGLT 2 inhibitor, GLP-1 recepter agonist, astrgaloside IV, huangkui capsule, ophiocordyceps sinensis
Citation
Elenjickal EJ, Valson AT, Varughese S, Vincent L, Fernando E and Natarajan G (2024) Editorial: Novel pathophysiologic mechanisms and reno-protective pharmacotherapies in diabetic kidney disease. Front. Pharmacol. 15:1531748. doi: 10.3389/fphar.2024.1531748
Received
20 November 2024
Accepted
02 December 2024
Published
11 December 2024
Volume
15 - 2024
Edited and reviewed by
Giuseppe Remuzzi, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Italy
Updates
Copyright
© 2024 Elenjickal, Valson, Varughese, Vincent, Fernando and Natarajan.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Elias John Elenjickal, sonyjohn84@gmail.com
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.