- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01195142
Adipose Tissue Gene Expression Profiles in Women With Polycystic Ovary Syndrome (PCOS) Versus Controls
3. september 2010 oppdatert av: The Adelaide and Meath Hospital
Adipose Tissue Gene Expression Profiles in Women With PCOS Versus Controls Matched for BMI
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.
Studieoversikt
Status
Fullført
Forhold
Detaljert beskrivelse
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.
Studietype
Observasjonsmessig
Registrering (Faktiske)
10
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Dublin, Irland, 24
- Diabetes Day Centre, The Adelaide and Meath Hosptial
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Leinster
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Dublin, Leinster, Irland, Dublin 4
- Nutrigenomics Group, University College Dublin
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 40 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Hunn
Prøvetakingsmetode
Ikke-sannsynlighetsprøve
Studiepopulasjon
Women with PCOS and a control population of women matched for age and body mass index (BMI)
Beskrivelse
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
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
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PCOS-CSAT
Women with PCOS
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Control-CSAT
Control population consisting of women without PCOS, matched for age and BMI with the PCOS cohort
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Transcriptomic profiling of subcutaneous adipose tissue of women with PCOS and age and BMI matched controls
Tidsramme: Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion
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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.
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Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Measurement of biomarkers of metabolic health (lipid, inflammatory markers) in plasma of PCOS cases and controls
Tidsramme: Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion
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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.
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Recruitment ran from Dec 2007-July 2008. Subjects attended the study location fasting on one occasion
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Helen M Roche, Dr, University College Dublin
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. desember 2007
Primær fullføring (Faktiske)
1. juli 2008
Studiet fullført (Faktiske)
1. juli 2008
Datoer for studieregistrering
Først innsendt
2. september 2010
Først innsendt som oppfylte QC-kriteriene
3. september 2010
Først lagt ut (Anslag)
6. september 2010
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
6. september 2010
Siste oppdatering sendt inn som oppfylte QC-kriteriene
3. september 2010
Sist bekreftet
1. juli 2008
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- DDC-UCD-ATCS
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .