Endometrial Hyperplasia Clinical Trial
Official title:
The Relation Between Serum Irisin Hormone Level and Endometrial Hyperplasia
The purpose of the study is to determine serum irisin hormone levels an its relation between endometrial hyperplasia
The study consisted of two groups. The first group was formed of the patients diagnosed
endometrial hyperplasia histopathologically , and the controls were healthy women admitted
to the clinic just for annual examination without any complain and symptoms. Patients in the
35-50 age range in both groups were included in the study. The histopathologic diagnosis of
patients was established for Kayseri Education and Research Hospital Pathology clinics.
Demographic parameters such as age, menopausal status, body mass index (BMI), body weight
and known familial cancer story were registered.
Pregnancy, liver function disorders, cardiovascular disease, metabolic disease, diabetes,
chronic kidney disease, central nerves system disease, immunosuppressive drug use, another
known malignancy and excessive exercises in among one month were all exclusion criteria for
the patients.
3 cc peripheral venous blood samples were taken in the patients' diagnosed endometrial
hyperplasia in the course of evaluation the biopsy results and in controls during their
examinations just for only once. Blood samples were centrifuged in 3200 rpm speed for 10
minutes, and stored in -80 'C until the analysis. Blood samples were evaluated on the same
day after four mounts for stored first blood sample. Serum Irisin levels were evaluated with
enzyme- linked immunosorbent assays kit (Catalog number: K4761-100 Biovision USA) in Kayseri
Research and Education Hospital Biochemical Clinics.
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Observational Model: Case Control, Time Perspective: Retrospective
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