Журнал кардиореспираторных исследований 2025. №3


Maqola mavzusi

CLINICAL AND GENETIC PREDICTION OF CHRONIC KIDNEY DISEASE RISK IN PATIENTS WITH METABOLIC SYNDROME (16-19)

Mualliflar

Mirzaev Rizamat Ziyadullaevich, Nosirova Dilangiz Akbarovna

Muassasa

Samarkand State Medical University

Annotatsiya

Due to the increasing prevalence of metabolic syndrome (MS) worldwide, predicting the risk of chronic kidney disease (CKD), one of the frequent complications of MS, has become particularly relevant. The purpose of this review article is to highlight current data on the relationship between MS and CKD, multicenter studies conducted, and genetic factors, as well as prospects for clinical and genetic prediction. Metabolic syndrome comprises a combination of abdominal obesity, arterial hypertension, carbohydrate metabolism disorders, and dyslipidemia. This syndrome independently affects the risk of kidney damage. According to an Iranian cohort study (15,255 participants), kidney damage associated with MS was detected with a hazard ratio (HR) of 1.51. A meta-analysis of 32 cohorts (over 400,000 observations) established that MS increases the risk of chronic renal failure by 47% (relative risk, RR = 1.47). A genetically determined decrease in estimated glomerular filtration rate (eGFR) has been confirmed in Mendelian randomization studies. An association between ALPK1, CDH4, and PTPRN2 genotypes and increased risk of CKD was observed in Japanese cohorts. These genes influence fat metabolism, insulin resistance, and chronic inflammation. Modern approaches include comprehensive assessment: clinical parameters (eGFR, albuminuria, C-reactive protein, HOMA-IR), genotyping, and artificial intelligence for constructing risk models. This opens up opportunities for early diagnosis and targeted therapy (RAAS blockade, SGLT2 inhibitors, metabolic correction).

Kalit so'zlar

metabolic syndrome, chronic kidney disease, genetic markers, risk prediction, gene polymorphisms, Mendelian randomization, insulin resistance, albuminuria, eGFR, clinical-genetic models

Adabiyotlar

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