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1.
Article in English | IMSEAR | ID: sea-177562

ABSTRACT

Polycystic ovary syndrome (PCOS) is a complex endocrine disorder affecting 18-22% of reproductiveaged women. According to the Rotterdam criteria, PCOS is diagnosed by any two of the following three criteria: oligo- or anovulation, clinical and/or biochemical hyperandrogenism, and polycystic ovaries. Four different phenotypes (A-D) of PCOS are identified assuming these three criteria. Heterogenous PCOS phenotypes might additionally include insulin resistance, hyperinsulinemia, hypertension, dyslipidemia, obesity, hirsutism, acne, infertility, as well as increased risk of metabolic syndrome and type 2 diabetes mellitus, decreased quality of life and impaired psychological function.As a promise, research suggests supplementing with inositol, former vitamin B-8, can help address various aspects of this condition.

2.
Article in English | IMSEAR | ID: sea-177529

ABSTRACT

Introduction: Suicide attempt (SA) is in the middle of continuum of complex suicidal behavior phenotype. Psychiatric disorders and acute stressful life events (SLEs) are triggers for suicidal behavior. Serotonin system genes are often implicated in suicidal behavior. Tryptophan hydroxylase 2 (TPH2), exclusively expressed in the brain, is the rate-limiting enzyme for serotonin biosynthesis. TPH2 may be enrolled in stress-response mechanisms via hypothalamic–pituitary–adrenal axis, while TPH2 variant rs7305115 has been reported to affect gene expression in postmortem human pons. To date, only poor examination of this variant in etiology of suicidal behavior has reported conflicting results. The aim of the present study was to assess rs7305115 main effect and its interaction with acute SLEs in SA pathology among Serbian psychiatric patients. Methods: 165 suicide attempters and 188 suicide non-attempters, suffering from major psychiatric disorders, participated in the study. Acute SLEs score was assessed using the List of Threatening Experiences Questionnaire. Variant rs7305115 was genotyped using TaqMan-based allelic discrimination assay. Statistical analyses were done in SNPstats by applying logistic regression adjusted by psychiatric diagnoses. Results: Variant rs7305115 was not associated with SA in Serbian psychiatric patients, neither alone, nor in combination with acute SLEs, for all five models of inheritance tested (P>0.05). Discussion: Our finding does not support the main and moderating implication of TPH2 variant rs7305115 in SA liability among Serbian psychiatric patients. Further examination in larger samples of this variant in SA patology is necessary due to its functional relevance.

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