In contrast to the decreasing burden related to cardiovascular disease (CVD), the burden related to dysglycemia and adiposity complications is increasing in Czechia, and local drivers must be identified. A comprehensive literature review was performed to evaluate biological, behavioral, and environmental drivers of dysglycemia and abnormal adiposity in Czechia. Additionally, the structure of the Czech healthcare system was described. The prevalence of obesity in men and diabetes in both sexes has been increasing over the past 30 years. Possible reasons include the Eastern European eating pattern, high prevalence of physical inactivity and health illiteracy, education, and income-related health inequalities. Despite the advanced healthcare system based on the compulsory insurance model with free-for-service healthcare and a wide range of health-promoting initiatives, more effective strategies to tackle the adiposity/dysglycemia are needed. In conclusion, the disease burden related to dysglycemia and adiposity in Czechia remains high but is not translated into greater CVD. This discordant relationship likely depends more on other factors, such as improvements in dyslipidemia and hypertension control. A reconceptualization of abnormal adiposity and dysglycemia into a more actionable cardiometabolic-based chronic disease model is needed to improve the approach to these conditions. This review can serve as a platform to investigate causal mechanisms and secure effective management of cardiometabolic-based chronic disease.

• Keywords
• adiposity, cardiometabolic risk, cardiovascular disease, chronic disease, dysglycemia, insulin resistance, nutrition, obesity, type 2 diabetes,
• MeSH
• Adiposity ethnology   MeSH
• White People statistics & numerical data   MeSH
• Chronic Disease epidemiology   ethnology   MeSH
• Diabetes Mellitus, Type 2 epidemiology   ethnology   MeSH
• Diet adverse effects   ethnology   MeSH
• Health Status Disparities MeSH
• Adult MeSH
• Dyslipidemias epidemiology   ethnology   MeSH
• Hypertension epidemiology   ethnology   MeSH
• Cardiometabolic Risk Factors MeSH
• Cardiovascular Diseases epidemiology   etiology   MeSH
• Middle Aged MeSH
• Humans MeSH
• Metabolic Syndrome epidemiology   ethnology   MeSH
• Obesity epidemiology   ethnology   MeSH
• Glucose Intolerance epidemiology   ethnology   MeSH
• Prediabetic State epidemiology   ethnology   MeSH
• Prevalence MeSH
• Sedentary Behavior ethnology   MeSH
• Social Determinants of Health ethnology   MeSH
• Feeding Behavior ethnology   MeSH
• Health Literacy MeSH
• Check Tag
• Adult MeSH
• Middle Aged MeSH
• Humans MeSH
• Male MeSH
• Female MeSH
• Publication type
• Journal Article MeSH
• Review MeSH
• Geographicals
• Czech Republic epidemiology   MeSH

BACKGROUND This study was carried out to determine the relationship between the common TMEM-18 (rs4854344, G>T) and NYD-SP18 (rs6971091, G>A) gene variants and weight loss after lifestyle interventions (increased physical activity in conjunction with optimal dietary intake) in overweight/obese children/adolescents. MATERIAL AND METHODS We genotyped 684 unrelated, white, non-diabetic children (age 12.7±2.1 years, average BMI at baseline 30.66±4.80 kg/m²). Anthropometric and biochemical examinations were performed before and after 4 weeks of an intensive lifestyle intervention. RESULTS The mean weight loss achieved was 5.20±2.02 kg (P<0.001). NYDSP-18 AA homozygotes had significantly higher abdominal skinfold value before and after the intervention (both, P=0.001). No significant associations between BMI decrease and the NYD-SP18 and TMEM18 variants were found. Associations between all anthropometrical and biochemical changes and genes remained non-significant after data were adjusted for sex, age, and baseline values. CONCLUSIONS Decreased body weight in overweight/obese children is not significantly influenced by the NYD-SP18 rs6971091 or TMEM18 rs4854344 polymorphisms.

• MeSH
• Adiposity genetics   MeSH
• Exercise MeSH
• Child MeSH
• Genotype MeSH
• Weight Loss genetics   MeSH
• Body Mass Index MeSH
• Nuclear Proteins genetics   metabolism   MeSH
• Polymorphism, Single Nucleotide MeSH
• Humans MeSH
• Membrane Proteins genetics   metabolism   MeSH
• Adolescent MeSH
• Overweight genetics   MeSH
• Obesity genetics   MeSH
• Body Weight genetics   MeSH
• Life Style MeSH
• Check Tag
• Child MeSH
• Humans MeSH
• Adolescent MeSH
• Male MeSH
• Female MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• FAM71F1 protein, human MeSH Browser
• Nuclear Proteins MeSH
• Membrane Proteins MeSH
• TMEM18 protein, human MeSH Browser