FEmale Metabolic Risk and Androgens: an Irish Longitudinal (FEMAIL) Study

Phase

N/A

Condition

Testotoxicosis

Testotoxikose

Metabolic Disorders

Treatment

Longitudinal follow up

Clinical Study ID

NCT04912648

20/49

Ages > 18
Female
Accepts Healthy Volunteers

Study Summary

Androgen excess is the cardinal biochemical feature of polycystic ovary syndrome (PCOS), a lifelong metabolic disorder affecting 10% of women. Serum testosterone correlates with insulin resistance in women, however, there is an urgent need to improve our understanding of the association between androgens and the risk of type 2 diabetes. Recently, a new subclass of androgenic steroids known as 11-oxygenated androgens has been identified. Utilising highly sensitive liquid chromatography-tandem mass spectrometry (LC-MS/MS) techniques, our group has recently demonstrated that 11-oxygenated steroids are the predominant androgens in both health controls and women with PCOS, and that these correlate closely with markers of insulin resistance. The bioactive 11-oxygenated androgen 11-ketotestosterone (11KT) binds and activates the androgen receptor with equal affinity to testosterone, yet nothing is known about its impact on metabolism or glucose homeostasis. Intriguingly, unlike testosterone, 11-oxygenated androgens do not decline with age in women, and, therefore, may mediate an increased risk of T2DM in women across their life course. Therefore, this previously ignored androgen class is likely of major importance in female metabolic health, and may represent a novel metabolic risk factor and biomarker. However, 11-oxygenated androgens are not currently measured in routine clinical practice. To date, no population-based or human in vivo physiology studies have examined the association between 11-oxygenated androgens, glucose metabolism and diabetes risk in women, despite the high prevalence of PCOS in the female population. There is emerging evidence, even in women without a confirmed history of PCOS, that the levels of androgens over time correlate with their likelihood of developing metabolic and cardiovascular disease. This has not been studied to date in a prospective manner in healthy women in the background population using long term follow up data.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Age 18 years or above
Ability to provide informed consent

Exclusion

Exclusion Criteria:

Pregnancy or breastfeeding at the time of planned recruitment
History of significant renal (eGFR<30) or hepatic impairment (AST or ALT >two-foldabove ULN; pre-existing bilirubinaemia >1.2 ULN)
The investigators will retain the right not to recruit potential participants withsevere health disorders which may impact on their ability to participate in the study;these may include, but are not limited to, metastatic cancer, severecardio-respiratory disease or other life-limiting health disorders
Participants who have participated in another research study involving aninvestigational medicinal product in the 12 weeks preceding the planned recruitment
Glucocorticoid use via any route within the last six months
Current intake of drugs known to impact upon steroid or metabolic function or intakeof such drugs during the six months preceding the planned recruitment
Use of combined oral hormonal contraception in the three months preceding the plannedrecruitment

Study Design

Longitudinal follow up

April 01, 2021

August 31, 2031

Study Description

Clinical questionnaire and baseline anthropometry:

Study investigators will complete a standardised case record form, with information obtained on relevant medical history, medications and anthropometric assessment (height, weight, body mass index, blood pressure, weight circumference). Body composition will be assessed using a portable bioimpedance machine (Tanita MC-780MA-S Portable). We will also obtain information on education level and household income. Participants will complete a standardised QOL questionnaire.

Serum, urine and saliva sampling:

Fasting bloods will be drawn for assessment of metabolic phenotype including glucose, insulin, lipid profile, full blood count, renal and liver biochemistry and HbA1C. Serum samples will also be obtained for measured of the steroid and non-targeted metabolome. Urine and saliva samples will be obtained for assessment of steroid metabolomics.

Targeted steroid metabolome profiling:

Serum, urinary and salivary multi-steroid profiling including classic and 11-oxygenated androgens will be performed using highly sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS). Furthermore, we will analyse the 24-h urine steroid metabolome, allowing for determination of 24-h net androgen output from classic and 11-oxygenated pathways (26). Analysis will be carried out by LC-MS/MS multi-steroid profiling. Multi-steroid profiling approaches have been developed and optimised at the University of Birmingham Steroid Metabolome Analysis Core (SMAC), where samples will be measured under the supervision of Professor Wiebke Arlt.

Non-targeted serum metabolomics:

The global non-targeted serum metabolome will be profiled at the Phenome Centre Birmingham under the supervision of Professor Warwick Dunn (co-applicant). Samples will be analysed applying Ultra Performance Liquid Chromatography (Ultimate3000RS; Thermo Scientific, Hemel Hempstead, UK) interfaced to an electrospray mass spectrometry (Q Exactive, Thermo Scientific, Hemel Hempstead, UK).

Muscle biopsy:

Under local anaesthetic and without using scalpel incision, muscle biopsies will be obtained from the vastus lateralis muscle of the leg in each participant. These will be performed using a Bard biopsy needle gun, with suction applied to increase tissue yield.

Recruitment:

Patients will be recruited via local advertising in Beaumont Hospital and RCSI Medical School.

Connect with a study center

Royal College of Surgeons in Ireland
Dublin, D9
Ireland
Active - Recruiting

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