2007
DOI: 10.1016/j.fertnstert.2007.01.032
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Risk of metabolic complications in the new PCOS phenotypes based on the Rotterdam criteria

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Cited by 179 publications
(161 citation statements)
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“…The prevalence of metabolic syndrome was 30-40 % in the study conducted by Shroff et al [20] and 35.07 % in Kar et al [15]. It is also observed that the prevalence of metabolic syndrome was higher in phenotype A in other studies [15,17,21]. Strongest positive association of metabolic syndrome was observed for systolic and diastolic blood pressure followed by waist circumference, triglyceride level, HDL level and lowest with fasting glucose levels.…”
Section: Discussionmentioning
confidence: 81%
“…The prevalence of metabolic syndrome was 30-40 % in the study conducted by Shroff et al [20] and 35.07 % in Kar et al [15]. It is also observed that the prevalence of metabolic syndrome was higher in phenotype A in other studies [15,17,21]. Strongest positive association of metabolic syndrome was observed for systolic and diastolic blood pressure followed by waist circumference, triglyceride level, HDL level and lowest with fasting glucose levels.…”
Section: Discussionmentioning
confidence: 81%
“…In turn, hyperinsulinemia stimulates androgens www. journals.viamedica.pl/ginekologia_polska synthesis in ovaries, closing the vicious circle [5]. Therefore, we have aimed at analyzing whether (TT/DHT) may be helpful in predicting metabolic risk not only in PCOS patients but also in healthy women not meeting PCOS criteria.…”
Section: Introductionmentioning
confidence: 99%
“…Por otro lado, se desconoce si este grupo de individuos posee los mismos riesgos cardiovasculares y reproductivos que las pacientes SOP según los criterios del NIH (7). En efecto, en un estudio retrospectivo cuyo objetivo eran determinar el riesgo relativo del SM en pacientes con SOP según los criterios de Rotterdam, se encontró que el fenotipo no androgénico de ovarios poliquísticos y oligoamneorrea (fenotipo D) presentaba el mismo riesgo que las pacientes controles sanas no SOP, incluso en las mujeres obesas (16). De esta forma, frente a la controversia de aumentar la heterogeneidad del SOP y con la débil evidencia disponible sobre los nuevos fenotipos, algunos grupos consideran muy prematuro adoptar los nuevos criterios de Rotterdam, ya que podrían significar efectos negativos a nivel de la práctica clínica, investigación científica y calidad de vida de las pacientes (14).…”
Section: Discussionunclassified
“…Desde este punto de vista, surge la interrogante sobre la validez de los dos nuevos fenotipos incorporados al síndrome, ovarios poliquísticos con oligoamenorrea y ovarios poliquísticos con hiperandrogenismo (fenotipos D y C). No está claro aún que estos últimos fenotipos, no así con los fenotipos NIH, posean igualmente mal pronóstico reproductivo o representen factores de riesgo cardiovascular a largo plazo, sobretodo con la ausencia de hiperandrogenismo (13,14,15,16).…”
Section: Discussionunclassified
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