PMID- 21655296 OWN - NLM STAT- MEDLINE DCOM- 20111005 LR - 20220129 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 6 IP - 5 DP - 2011 TI - Circulating vascular progenitor cells and central arterial stiffness in polycystic ovary syndrome. PG - e20317 LID - 10.1371/journal.pone.0020317 [doi] LID - e20317 AB - OBJECTIVE: Subjects with Polycystic ovarian syndrome (PCOS) are at increased risk of Type 2 diabetes mellitus (T2DM). The mechanism of this enhanced risk is unclear. Circulating vascular progenitor cells (VPC) are immature bone marrow derived cells capable of differentiating into mature endothelial cells. VPC number/function and central arterial stiffness predict cardio-metabolic disease in at-risk populations. DESIGN: We studied VPC and arterial stiffness measures in non-obese PCOS subjects as compared to age and body mass index (BMI) matched healthy controls in a cross-sectional study. METHODS: Fourteen subjects with PCOS and 12 controls of similar age, BMI (all <30 kg/m(2)) and metabolic profile were studied. VPC number and in vitro function were studied by flow cytometry and tube formation assays respectively. Augmentation index (AIx), a measure of central arterial stiffness, and central (aortic) blood pressures (BP) were measured by applanation tonometry. RESULTS: Subjects with PCOS had a reduced number, mean+/-SEM, of circulating CD34(+)133(+) VPCs (317.5+/-51.0 vs. 558.3+/-101.2, p = 0.03) and impaired in vitro tube formation (completed tube area 1.0+/-0.06 vs. 1.2+/-0.05x10(6) microm(2) p = 0.02). PCOS subjects had significantly higher AIx (18.4+/-1.9% vs. 4.9+/-2.0%) and this difference remained significant even after adjustments for age, BMI and smoking (p = 0.003) in multivariate analyses. Central systolic and pulse pressure were higher in PCOS subjects but these differences were not statistically significant after adjustment for age. Brachial systolic and pulse pressures were similar. VPC number/function and arterial stiffness or BP measures were not correlated. CONCLUSIONS: Non-obese PCOS is characterized by a reduced VPC number, impaired VPC function and increased central arterial stiffness. These changes in novel vascular risk markers may explain the enhanced risk of T2DM and CVD in PCOS. FAU - Dessapt-Baradez, Cecile AU - Dessapt-Baradez C AD - Cardiovascular Division at Guy's and St Thomas and King's College Hospitals, King's College London, London, United Kingdom. cecile.dessapt@kcl.ac.uk FAU - Reza, Maria AU - Reza M FAU - Sivakumar, Ghayathri AU - Sivakumar G FAU - Hernandez-Fuentes, Maria AU - Hernandez-Fuentes M FAU - Markakis, Kostas AU - Markakis K FAU - Gnudi, Luigi AU - Gnudi L FAU - Karalliedde, Janaka AU - Karalliedde J LA - eng GR - Wellcome Trust/United Kingdom GR - G0801537/MRC_/Medical Research Council/United Kingdom PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20110531 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (AC133 Antigen) RN - 0 (Antigens, CD) RN - 0 (Antigens, CD34) RN - 0 (Glycoproteins) RN - 0 (Peptides) SB - IM MH - AC133 Antigen MH - Adult MH - Antigens, CD/metabolism MH - Antigens, CD34/metabolism MH - Arteries/physiopathology MH - Body Mass Index MH - Cross-Sectional Studies MH - Endothelial Cells/cytology/*physiology MH - Female MH - Glycoproteins/metabolism MH - Humans MH - Peptides/metabolism MH - Polycystic Ovary Syndrome/blood/*physiopathology MH - Stem Cells/cytology/*physiology MH - Young Adult PMC - PMC3105021 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2011/06/10 06:00 MHDA- 2011/10/06 06:00 PMCR- 2011/05/31 CRDT- 2011/06/10 06:00 PHST- 2011/01/21 00:00 [received] PHST- 2011/04/22 00:00 [accepted] PHST- 2011/06/10 06:00 [entrez] PHST- 2011/06/10 06:00 [pubmed] PHST- 2011/10/06 06:00 [medline] PHST- 2011/05/31 00:00 [pmc-release] AID - PONE-D-11-01740 [pii] AID - 10.1371/journal.pone.0020317 [doi] PST - ppublish SO - PLoS One. 2011;6(5):e20317. doi: 10.1371/journal.pone.0020317. Epub 2011 May 31.