Primary research questionDo obese PCOS women with reduced insulin sensitivity have HDL particles that have impaired anti-oxidative function in comparison with lean controls with normal insulin sensitivity?Secondary research questionDo obese PCOS…
ID
Source
Brief title
Condition
- Endocrine disorders of gonadal function
- Ovarian and fallopian tube disorders
- Arteriosclerosis, stenosis, vascular insufficiency and necrosis
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Difference in anti-oxidative capacity of HDL between obese PCOS women with
reduced insulin sensitivity and lean controls with normal insulin sensitivity.
During oxidation of LDL conjugated dienes are released. Addition of HDL can
inhibit the rate of oxidation of LDL; as a consequence less conjugated diens
are being released.
In the current study, the difference in conjugated dienes between PCOS and
controls will be compared.
NB the anti-oxidative capacity of HDL is measured and expressed independently
of the total amount of HDL
Secondary outcome
Difference in composition of HDL between obese PCOS women with reduced insulin
sensitivity and lean controls with normal insulin sensitivity.
The composition of HDL particles.
Using ultracentrifugation subfractions of HDL will be isolated:
HDL2a,2b,3a,3b,3c. In these fractions cholesterol, triglycerides, phospholipids
and apolipoproteins will be determined.
The composition of these subfractions will be compared between PCOS and
controls.
As an exploratory parameter the number of endothelial progenitor cells will be
determined in PCOS and in controls.
Background summary
The polycystic ovary syndrome (PCOS) is characterised by oligo-amenorhea,
clinical or biochemical hyperandrogenism and polycystic ovaries on ultrasound.
It affects approximately 5 % of premenopausal women. PCOS is associated with
insulin resistance, dyslipidemia and abnormal surrogate endpoints for
atherosclerosis. Several patterns of dyslipidemia have been described in PCOS;
low high density lipoprotein (HDL)-cholesterol is a frequent finding.
HDL particles play an important role in the protection against atherosclerosis,
in part by their anti-oxidative capacity. The composition of an HDL particle is
a determinant of its function.
Both insulin resistance and low levels of plasma HDL-cholesterol have been
associated with impaired anti-oxidative function of HDL particles in
predominantly male study populations. No studies of anti-oxidative function of
HDL in women have been performed yet.
We hypothesize that PCOS women, who are often obese and insulin resistant, and
frequently have low plasma HDL-cholesterol, have impaired (composition and)
anti-oxidative function of HDL particles, contributing to their cardiovascular
risk.
Endothelial progenitor cells (EPC*s) are involved in endothelial repair. The
circulating number of EPC*s is reduced in patients with cardiovascular risk
factors, such as insulin resistance. We hypothesize that PCOS women, who are
often insulin resistant, have lower circulating numbers of EPC*s than controls.
Study objective
Primary research question
Do obese PCOS women with reduced insulin sensitivity have HDL particles that
have impaired anti-oxidative function in comparison with lean controls with
normal insulin sensitivity?
Secondary research question
Do obese PCOS women with reduced insulin sensitivity have a different
composition of HDL particles in comparison with lean controls with normal
insulin sensitivity?
Explorative research question
Do obese PCOS women with reduced insulin sensitivity have lower numbers of
circulating endothelial progenitor cells (EPC*s) in comparison with lean
controls with normal insulin sensitivity?
Study design
Case-control
Study burden and risks
Questionaire on cardiovascular risk factors.
Physical examination: height, weight, waist- en hip circumference
Vena punction: max 50 ml blood
Abnormal values for cholesterol, triglycerides or glucose could be found,
requiring further investigation and treatment.
Burden and risk are estimated to be low.
Heidelberglaan 100
3584 CX Utrecht
Nederland
Heidelberglaan 100
3584 CX Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
Cases: PCOS+, BMI >=27, HOMA >=1.5, 25-40 years of age
Controls: PCOS-, BMI<25, HOMA <1,5 25-40 years of age
Exclusion criteria
Diabetes mellitus
Oral contraceptives
Lipid lowering medication
Pregnancy
Familial hypercholesterolemia
Hypertriglyceridemia
Clinically manifest cardiovascular disease
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL14897.041.06 |