Excess Metabolic and Cardiovascular Risk is not Manifested in all Phenotypes of Polycystic Ovary Syndrome: Implications for Diagnosis and Treatment
Autor: | Athanasia Piouka, Artemis Karkanaki, Dimitrios Panidis, Georgios N. Daskalopoulos, Paraschos Gkeleris, Nikolaos Prapas, Vasilios G. Athyros |
---|---|
Rok vydání: | 2015 |
Předmět: |
Adult
medicine.medical_specialty Overweight Body Mass Index Young Adult Non-alcoholic Fatty Liver Disease Risk Factors Internal medicine medicine Humans cardiovascular diseases Obesity Young adult Pharmacology Metabolic Syndrome biology business.industry C-reactive protein Fatty liver Case-control study nutritional and metabolic diseases medicine.disease Atherosclerosis Polycystic ovary female genital diseases and pregnancy complications Endocrinology C-Reactive Protein Phenotype Cardiovascular Diseases Case-Control Studies biology.protein Female Metabolic syndrome medicine.symptom Cardiology and Cardiovascular Medicine business Body mass index Polycystic Ovary Syndrome |
Zdroj: | Current vascular pharmacology. 13(6) |
ISSN: | 1875-6212 |
Popis: | Aim: To assess the potential differences in the metabolic and cardiovascular disease (CVD) risk between the distinct phenotypes of the Polycystic Ovary Syndrome (PCOS) according to the Rotterdam definition regardless of body mass index (BMI). Patients-Methods: The study included 300 women; 240 women with PCOS, according to the Rotterdam criteria and 60 controls without PCOS. All women were further subdivided, according to their BMI, into normal-weight and over- weight/obese and PCOS women were furthermore subdivided in 4 phenotypes of the syndrome. A complete hormonal and metabolic profile as well as the levels of high sensitivity C reactive protein (hsCRP) and lipoprotein-associated phospholi- pase A2 (Lp-PLA2) were measured. Outcomes: Levels of surrogate markers of subclinical atherosclerosis (hsCRP and Lp-PLA2), levels of evaluated CVD risk score using risk engines, and several correlations of CVD risk factors. Results: hsCRP levels were higher but not significantly so in PCOS women compared with controls. In lean PCOS pa- tients, Lp-PLA2 levels were significantly higher, compared with lean controls, mainly in the 2 classic phenotypes. Over- weight/obese patients in all 4 phenotypes had significantly higher Lp-PLA2 levels compared with overweight/obese con- trols. Evaluated CVD risk according to 4 risk engines was not different among phenotypes and between PCOS patients and controls. There were several correlations of risk factors with metabolic syndrome and non-alcoholic fatty liver disease requiring appropriate treatment. Conclusion: Only 2 of 4 Rotterdam phenotypes, identical with those of the classic PCOS definition, have excess car- diometabolic risk. These need to be treated to prevent CVD events. |
Databáze: | OpenAIRE |
Externí odkaz: |