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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01195142
Other study ID # DDC-UCD-ATCS
Secondary ID
Status Completed
Phase N/A
First received September 2, 2010
Last updated September 3, 2010
Start date December 2007
Est. completion date July 2008

Study information

Verified date July 2008
Source The Adelaide and Meath Hospital
Contact n/a
Is FDA regulated No
Health authority Ireland: Research Ethics Committee
Study type Observational

Clinical Trial Summary

Adipose tissue is a central organ in mediating metabolic health. There is some evidence that women with polycystic ovary syndrome (PCOS) have a degree of adipose tissue dysfunction which may negatively affect their metabolic health. The aim of this study was to assess transcriptomic profiles of subcutaneous adipose tissue of women with PCOS in comparison with a control population matched on the basis of age and body mass index (BMI). A secondary aim was to then relate these gene expression profiles to the biochemical environment.


Description:

Adipose tissue is a central organ in mediating metabolic health. There is some evidence that women with polycystic ovary syndrome (PCOS) have a degree of adipose tissue dysfunction which may negatively affect their metabolic health. The aim of this study was to assess transcriptomic profiles of subcutaneous adipose tissue of women with PCOS in comparison with a control population matched on the basis of age and body mass index (BMI). A secondary aim was to then relate these gene expression profiles to the biochemical environment.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Had a positive diagnosis of PCOS as defined according to the NIH criteria as chronic oligomenorrhoea (< 9 menstrual cycles per year) and clinical and/or biochemical evidence of hyperandrogenism, in the absence of other disorders causing the same phenotype. Clinical criteria included hirsutism with a Ferriman-Galwey score greater than 9, acne or male pattern alopecia; biochemical criteria included total-testosterone, androstenedione or dehydroepiandrosterone sulphate (DHEAS) greater than the laboratory reference range.

- Were between the ages of 18 and 40

Exclusion Criteria:

- Were under 18 years or greater than 40 years old,

- Were non-Caucasian

- Were pregnant, lactating or trying to conceive

- Had a body mass index (BMI) <18kg/m2 or >50kg/m2

- Had a recent illness or any chronic illness likely to influence results

- Were taking hormonal contraception

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Ireland Diabetes Day Centre, The Adelaide and Meath Hosptial Dublin
Ireland Nutrigenomics Group, University College Dublin Dublin Leinster

Sponsors (2)

Lead Sponsor Collaborator
The Adelaide and Meath Hospital University College Dublin

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Transcriptomic profiling of subcutaneous adipose tissue of women with PCOS and age and BMI matched controls Gene expression profiles from women with PCOS and controls matched for age and BMI were determined by microarray analysis of whole subcutaneous adipose tissue samples. Single gene changes as well as pathway analyses will be used to determine differently expressed genes and pathways between the PCOS cohort and controls. Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion No
Secondary Measurement of biomarkers of metabolic health (lipid, inflammatory markers) in plasma of PCOS cases and controls Biomarkers of metabolic health were assessed in plasma of women with PCOS and age and BMI matched controls. Lipid profile, hormonal profile, various key inflammatory markers and adipokines will be measured. Glucose and insulin concentrations will be assessed also. All parameters will be assessed following a 12 hour over night fast at the study location. Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion No
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