DENSITY ANALYSIS OF THE INTEGRATION OF HYPERURICEMIA INTO THE CLUSTER OF RISK FACTORS FOR GLUCOSE HOMEOSTASIS DISORDERS ASSOCIATED WITH METABOLIC SYNDROME AT THE LEVEL OF A RANDOM POPULATION SAMPLE

Authors

  • Cherniaieva A. O. SI «V. Danilevsky Institute for Endocrine Pathology Problems of the NAMS of Ukraine»; Kharkiv, Ukraine; Kharkiv National Medical University, Kharkiv, Ukraine https://orcid.org/0000-0002-2812-3323
  • Mykytyuk M. R. SI «V. Danilevsky Institute for Endocrine Pathology Problems of the NAMS of Ukraine»; Kharkiv, Ukraine https://orcid.org/0000-0002-6169-7628
  • Karachentsev SI «V. Danilevsky Institute for Endocrine Pathology Problems of the NAMS of Ukraine»; Kharkiv, Ukraine; Kharkiv National Medical University, Kharkiv, Ukraine https://orcid.org/0000-0003-1317-6999

DOI:

https://doi.org/10.21856/j-PEP.2026.1.05

Keywords:

uric acid, hyperuricemia, purine dysmetabolism, insulin resistance, metabolic syndrome, impaired glucose homeostasis, random population sample, obesity, cardiovascular risk

Abstract

Background. Hyperuricemia, as one of the key components of the metabolic syndrome in the population, can be assessed only under certain conditions. Hyperuricemia in the context of the metabolic syndrome is understood as a serum uric acid concentration in accordance with population norms. At the same time, according to the EULAR recommendations, the criteria for verification of hyperuricemia are more stringent and aimed at diagnosing gout, in which the serum uric acid concentration is pathologically high.
Research objective – to analyze the density of integration of hyperuricemia into the cluster of risk factors for glucose homeostasis disorders associated with metabolic syndrome, and to provide a quantitative assessment of the relationship between hyperuricemia and the main components of metabolic syndrome at the level of a random population sample.
Materials and methods. According to generally accepted epidemiological approaches random population sample of 727 in­di­viduals was formed. Metabolic syndrome was diagnosed according to IDF criteria (2006).
Results. Hyperuricemia (HU) was detected in 16.23 % of people in the studied random population sample (RPS). It was found that with. The relationship between serum uric acid (UA) concentration and age, the studied parameters of glucose homeostasis, blood lipid spectrum, cardiovascular risk, liver and kidney function in RPS representatives with overweight/obesity (BMI ≥25 kg/m2) does not depend on any of the selected stratification criteria (gender, BMI, and degree of obesity). Each of the selected clinical and biochemical parameters can be considered both a cause and a consequence of HU in overweight/obese individuals in the RPS. According to the results of factor analysis, it was determined that serum UA concentration in RPS representatives is asso­ciated with age, abdominal obesity, liver and kidney function. The established density of the connection of the HU with other components of the metabolic syndrome does not allow considering the HU as a component of the metabolic syndrome in the RPS.
Conclusions. Hyperuricemia in random population sample representatives is associated with age, abdominal obesity and insulin resistance and is not related to the "classic" components of metabolic syndrome (glucose homeostasis disorders, arterial hypertension, dyslipidemia) and does not act as a synergistic factor between them. In random population sample representatives with excess body weight/obesity, regardless of gender, serum uric acid concentration is associated with age, parameters of glucose homeostasis, blood lipid spectrum, with cardiovascular risk, functional state of the liver and kidneys.

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Published

2026-03-15

How to Cite

Cherniaieva, A., Mykytyuk, M., & Karachentsev, Y. (2026). DENSITY ANALYSIS OF THE INTEGRATION OF HYPERURICEMIA INTO THE CLUSTER OF RISK FACTORS FOR GLUCOSE HOMEOSTASIS DISORDERS ASSOCIATED WITH METABOLIC SYNDROME AT THE LEVEL OF A RANDOM POPULATION SAMPLE. Problems of Endocrine Pathology, 83(1), 42–51. https://doi.org/10.21856/j-PEP.2026.1.05

Issue

Section

CLINICAL ENDOCRINOLOGY

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