Biochemical and Biophysical Research Communications, Journal Year: 2024, Volume and Issue: 745, P. 151086 - 151086
Published: Dec. 24, 2024
Language: Английский
Biochemical and Biophysical Research Communications, Journal Year: 2024, Volume and Issue: 745, P. 151086 - 151086
Published: Dec. 24, 2024
Language: Английский
Journal of Clinical Medicine, Journal Year: 2025, Volume and Issue: 14(3), P. 727 - 727
Published: Jan. 23, 2025
Diabetic Kidney Disease (DKD) is the leading cause of end-stage renal disease (ESRD) worldwide. Among individuals with type 1 diabetes mellitus (T1DM), 30–40% are at risk developing DKD. This review focuses on mechanistic processes, available and emerging biomarkers for diagnosing, monitoring, preventing DKD, as well treatment options targeted DKD patients. A literature search was conducted PubMed Scopus using specific keywords. Inclusion exclusion criteria were applied to select articles used this review. The highlights various mechanisms involved in progression more severe stages. Additionally, several have been identified, which aid diagnosing monitoring disease. Furthermore, numerous approaches being explored address underlying causes Advanced research exploring new medications remission; sodium-glucose cotransport (SGLT2) inhibitors finerenone, particular, gaining attention their novel renoprotective effects. a major complication diabetes, marked by complex multifactorial mechanisms. Thus, understanding these processes essential therapies potentially reverse progression. Biomarkers show promise early diagnosis progression, while current strategies underscore importance multifaceted approach.
Language: Английский
Citations
2Phytochemistry Reviews, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 27, 2025
Language: Английский
Citations
1Molecular Biomedicine, Journal Year: 2025, Volume and Issue: 6(1)
Published: March 22, 2025
Abstract Klotho, initially introduced as an anti-aging protein, is expressed in the brain, pancreas, and most prominently kidney. The two forms of Klotho (membrane-bound soluble form) have diverse pharmacological functions such anti-inflammatory, anti-oxidative, anti-fibrotic, tumour-suppressive etc. membrane-bound form plays a pivotal role maintaining kidney homeostasis by regulating fibroblast growth factor 23 (FGF 23) signalling, vitamin D metabolism phosphate balance. deficiency has been linked with significantly reduced protection against various pathological phenotypes, including diabetic disease (DKD), which major cause chronic leading to end-stage disease. Owing pleiotropic actions klotho, it shown beneficial effects DKD tackling complex pathophysiology reducing inflammation, oxidative stress, well fibrosis. Moreover, protective effect klotho extends beyond other conditions, cardiovascular diseases, alzheimer's disease, cancer, inflammatory bowel liver Therefore, this review summarizes relationship between expression diseases special emphasis on DKD, distinct mechanisms potential exogenous supplementation therapeutic strategy. Future research into could unravel novel treatment avenues for diseases.
Language: Английский
Citations
1Biochemical and Biophysical Research Communications, Journal Year: 2025, Volume and Issue: unknown, P. 151711 - 151711
Published: March 1, 2025
Language: Английский
Citations
1Hormone and Metabolic Research, Journal Year: 2024, Volume and Issue: unknown
Published: Nov. 21, 2024
Abstract Diabetic nephropathy represents a predominant etiology of end-stage renal disease (ESRD) on global scale, significantly impacting the morbidity and mortality rates individuals with diabetes. The primary objective this analysis is to furnish comprehensive examination etiology, fundamental mechanisms, treatment modalities for DN. development DN stems from multitude factors, encompassing intricate interplay involving metabolic irregularities induced by hyperglycemia, alterations in hemodynamics, inflammatory responses, oxidative stress, genetic susceptibility. Principal mechanisms encompass generation advanced glycation end products (AGEs), activation protein kinase C (PKC), overexpression renin-angiotensin-aldosterone system (RAAS). These processes precipitate glomerular hyperfiltration, hypertrophy, eventually, fibrosis scarring parenchyma. Initially, hyperglycemia triggers mesangial proliferation thickening basement membrane incipient stages DN, subsequently leading progressive sclerosis tubulointerstitial fibrosis. Inflammatory cascades, notably cytokines like TGF-β NF-κB, play pivotal roles advancement fostering accumulation extracellular matrix Inflammation pathways, particularly those essential diabetic progression stimulating presence worsened dysfunctional mitochondria, contributes further injury via lipid peroxidation DNA damage. Current therapeutic approaches concentrate optimizing glycemic control, controlling hypertension, suppressing system. Among antihypertensive medications, ACE inhibitors angiotensin II receptor blockers are crucial decelerating advancement.
Language: Английский
Citations
4Frontiers in Pharmacology, Journal Year: 2025, Volume and Issue: 15
Published: Jan. 3, 2025
Diabetic kidney disease (DKD) has become the leading cause of end-stage renal in world. However, current conventional approaches have not yet achieved satisfactory efficacy. As one most influential products botanical medicine, Ginkgo biloba L. leaves extract (GBE) demonstrates various pharmacological effects on DKD and is gradually used as an adjunctive therapy for this disease. A comprehensive analysis necessary to evaluate efficacy safety GBE adjuvant treatment DKD. This meta-analysis aimed a supplementary renin-angiotensin-aldosterone system inhibitors patients, providing reference subsequent research clinical practice. study been registered PROSPERO CRD42023455792. Ten databases were searched from their inception 21 July 2023. Randomized controlled trials about included. Review Manager 5.4 Stata 16.0 employed conduct analysis. Heterogeneity was assessed through χ2 test I2 test, effect model chosen accordingly. Meta-regression subgroup performed investigate sources heterogeneity influence different factor levels The publication bias evaluated with funnel plot Egger's evidence quality by Grading Recommendations Assessment, Development Evaluation (GRADE) method. total 41 studies 3,269 patients finally enrolled study. None included reported whether or cardiovascular progression events occurred. Compared angiotensin-converting enzyme inhibitor (ACEI)/angiotensin II receptor blocker (ARB) alone, combination more beneficial improving urinary albumin excretion rate (UAER) [mean difference (MD) = -22.99 μg/min, 95% confidence interval (CI): -27.66 -18.31, p < 0.01], serum creatinine (SCr) [MD -8.30 μmol/L, CI: -11.55 -5.05, blood urea nitrogen (BUN) -0.77 mmol/L, -1.04 -0.49, 24-hour protein (24hUTP) -0.28 g/d, -0.35 -0.22, cystatin C (Cys-C) -0.30 mg/L, -0.43 -0.17, cholesterol (TC) -0.69 -1.01 -0.38, triglyceride (TG) -0.40 -0.56 -0.23, low-density lipoprotein (LDL-C) -0.97 -1.28 -0.65, fasting glucose (FBG) -0.54 -0.05, 0.02], hematocrit -4.58%, -5.25 -3.90, 0.01] fibrinogen -0.80 g/L, -1.12 -0.47, 0.01]. No significant improvement found 2-hour postprandial (2hPG), glycated hemoglobin (HbA1c), diastolic pressure (DBP) systolic (SBP). detected adverse events. Combining ACEI/ARB may improve UAER, SCr, BUN, 24hUTP, Cys-C, TC, TG, LDL-C, patients. It also seems oxidative stress inflammation but minimal impact pressure. Combined generally tolerated, monitoring remains essential during its use. More long-term high-quality in-depth molecular are still provide stronger regarding benefits https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=455792, identifier
Language: Английский
Citations
0World Journal of Diabetes, Journal Year: 2025, Volume and Issue: 16(3)
Published: Jan. 20, 2025
BACKGROUND Serum retinol-binding protein (RBP) is the primary transport of circulating vitamin A. RBP has a crucial role in maintaining nutrient metabolism and physiologic homeostasis. Several studies have indicated that serum participates progression diabetes diabetes-related complications. However, impact on lower limb atherosclerosis not been determined individuals with type 2 mellitus (T2DM). AIM To determine association between T2DM. METHODS This retrospective study enrolled 4428 eligible T2DM patients divided into non-lower (n = 1913) groups 2515) based arterial ultrasonography results. At hospital admission, baseline levels were assessed, all subjects categorized three (Q1-Q3) tertiles. Logistic regression, restricted cubic spline subgroup analysis, machine learning used to assess risk. RESULTS Among T2DM, 2515 (56.80%) had atherosclerosis. analysis showed risk increased by 1% for every 1 unit rise level (odds ratio 1.01, 95% confidence interval: 1.00-1.02, P 0.004). Patients highest tertile group (Q3) higher compared lowest (Q1) 1.36, 1.12-1.67, 0.002). The gradually an increase (P trend 0.005). Restricted linear correlation (non-linear < 0.05). Machine demonstrated significance diagnostic value predicting CONCLUSION Elevated correlate
Language: Английский
Citations
0Scientific Reports, Journal Year: 2025, Volume and Issue: 15(1)
Published: Feb. 4, 2025
Diabetic nephropathy (DN) is one of the major causes end-stage renal disease. This study aimed to explore internal relationship between metabolic processes and autoimmune responses in patients with DN via untargeted metabolomics Olink proteomics. The serum 10 who were diagnosed healthy individuals Animal models used validate characterized genes. Correlation analysis differentially abundant metabolites expressed proteins revealed that SIRT2 might be a key hub linking energy metabolism innate immune responses. KEGG enrichment showed HIF-1 signaling pathway cell carcinoma co-enriched pathways inflammatory response. VEGFA plays vital role these two pathways. ability regulate expression has been demonstrated. In vivo experiments SIRT2, VEGFA, HIF-1α highly kidneys mice diabetic nephropathy. conclusion, our combines proteomics provide valuable insights into synergistic roles disorders DN. data suggest may target affecting processes.
Language: Английский
Citations
0Published: Jan. 1, 2025
Language: Английский
Citations
0Journal of Ethnopharmacology, Journal Year: 2025, Volume and Issue: unknown, P. 119506 - 119506
Published: Feb. 1, 2025
Language: Английский
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