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    Baseline and longitudinal determinants of survival in end-stage renal disease: A joint longitudinal–survival analysis

    Saudi Journal of Kidney Diseases and Transplantation. October 14, 2026

    Introduction:

    Evidence remains limited regarding how repeated biomarker measurements influence survival in individuals with end-stage renal disease (ESRD). This study examined the prognostic role of both baseline biomarker levels and their longitudinal patterns in ESRD patients.

    Materials and Methods:

    This retrospective cohort included maintenance hemodialysis patients from Shahid Ayatollah Ashrafi Esfahani Hospital, Tehran, Iran, with at least 3 months of dialysis history. Cox regression assessed baseline predictors, while a joint longitudinal–survival model evaluated repeated albumin, hemoglobin, Kt/V, and urea reduction ratio (URR) measurements in relation to survival.

    Results:

    Overall, 330 ESRD patients were analyzed, with a mean age of 55.63 ± 15.57 years. In the joint model, each one-unit increase in the estimated current value of albumin, hemoglobin, Kt/V, and URR was linked to a lower risk of mortality over follow-up, with hazard ratios of 0.996 (P = 0.009), 0.999 (P = 0.015), 0.994 (P = 0.039), and 0.988 (P = 0.043), respectively. In Cox regression, higher white blood cell count increased mortality risk (Hazard ratio [HR]: 1.09, P = 0.025), whereas higher baseline log-ferritin, hemoglobin, and URR reduced risk, with HRs of 0.83 (P = 0.042), 0.85 (P < 0.001), and 0.13 (P = 0.035), respectively.

    Conclusions:

    The current study showed that longitudinal changes in markers such as albumin, hemoglobin, Kt/V, and URR may be important predictors of survival in patients with ESRD. Evaluation of baseline marker levels, along with longitudinal changes, nutritional status, age, and body mass index, may be important for determining survival among patients with ESRD.

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    Renoprotective Effects of AdipoRon in Preclinical Models of Renal Injury: A Systematic Review and Meta-Analysis

    Saudi Journal of Kidney Diseases and Transplantation. September 01, 2026

    Background:

    AdipoRon has shown promising metabolic and anti-inflammatory effects by activating the AMPK and PPARα pathways. However, its renal effects have not been systematically assessed. This study aimed to evaluate the efficacy of AdipoRon in mitigating renal injury based on preclinical evidence.

    Methods:

    A comprehensive systematic literature search was conducted in accordance with the PRISMA 2020 guidelines. We searched PubMed, Embase, Web of Science, Scopus, and Cochrane Central for publications up to December 2025. The SYstematic Review Centre for Laboratory animal Experimentation (SYRCLE) tool was used to evaluate the risk of bias of the included studies. Quantitative synthesis was performed using RevMan 5.4.1, employing standardized mean differences (SMDs) with 95% confidence intervals (CIs) under random-effects models. Heterogeneity was assessed using the I2 statistic.

    Results:

    Eight studies met the inclusion criteria for qualitative synthesis, and four provided extractable data for meta-analysis. AdipoRon significantly reduced albuminuria (SMD = –2.64, 95% CI –3.41 to –1.87, p < 0.001) and triglyceride levels (SMD = –1.65, 95% CI –2.28 to –1.01, p < 0.001) with negligible heterogeneity. Mechanistic analyses indicated that AdipoRon attenuated oxidative stress, inflammation, apoptosis, and fibrosis by activating the AMPK and PPARα signalling pathways.

    Conclusions:

    AdipoRon demonstrated consistent nephroprotective effects in preclinical models, primarily through metabolic and anti-inflammatory modulation. Despite heterogeneity in some outcomes, findings support its potential as a candidate for renal protection. Further standardized and translational studies are needed to confirm these effects in clinical settings.

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    Nephrotic range proteinuria in adults: Clinicopathological experience from a single institute in rural North India

    Saudi Journal of Kidney Diseases and Transplantation. September 01, 2026

    Background:

    The western literature is increasingly reporting focal segmental glomerulosclerosis overtaking membranous nephropathy as the leading cause of nephrotic range proteinuria in adults. However, data from a socioeconomically and geographically diverse nation like India are limited and does not entirely align with Western observations. We undertook this study to evaluate the spectrum of glomerular diseases presenting as nephrotic range proteinuria in adults, and to establish its clinico-pathological correlation.

    Methods:

    Ninety patients presenting with adult-onset nephrotic range proteinuria, who underwent USG-guided percutaneous renal biopsy, were evaluated clinically and histopathologically over 4 years in a tertiary care centre in north India.

    Results:

    The majority (28.9%) of patients were in 18-28 years age group (mean age, 39.36 years), with a 1.7:1 male-to-female ratio. The most common presenting complaint was generalised body swelling/pedal oedema (94.4%). Podocytopathy, including non-proliferative glomerulopathy suggestive of minimal change disease (26.6%) and focal segmental glomerulosclerosis (15.6%) combined, constituted the largest category (42.2%) of glomerular diseases manifesting as nephrotic range proteinuria in adult patients. Membranous nephropathy accounted for 23.33% of cases. The other etiologies included 13 (14.4%) cases of IgA nephropathy, 6 (6.6%) cases each of diabetic nephropathy and immune complex-mediated membranoproliferative glomerulonephritis, 4 (4.4%) cases of AA-type amyloidosis, and 2 (2.2%) cases of lupus nephritis.

    Conclusion:

    Our study reinforces that the etiologic spectrum of adult-onset nephrotic range proteinuria in India did not entirely mirror Western trends. Podocytopathies represented the largest category, emphasising the ongoing epidemiologic transition in glomerular diseases, advocating a need for continued regional surveillance and multicenter data integration.

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