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Circulating endothelial progenitor cells in acromegaly.

G Bellastella1, M I Maiorino, R Pivonello

  • 1Unit of Metabolic Diseases, Department of Geriatrics and Metabolic Diseases, Second University of Naples, Naples, Italy.

Journal of Endocrinological Investigation
|June 27, 2013
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Summary

Acromegaly patients have increased levels of circulating endothelial progenitor cells (EPCs), which are crucial for vascular repair. These elevated EPCs, particularly those expressing KDR, are positively correlated with insulin-like growth factor I (IGF-I) levels.

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Area of Science:

  • Endocrinology
  • Vascular Biology
  • Cell Biology

Background:

  • Endothelial progenitor cells (EPCs) are vital for vascular repair and correlate with insulin-like growth factor I (IGF-I) in healthy individuals.
  • The levels and function of EPCs in acromegaly, a condition of excess growth hormone and IGF-I, remain uninvestigated.

Purpose of the Study:

  • To investigate the levels of circulating EPC phenotypes in patients with acromegaly.
  • To explore the relationship between EPC levels and IGF-I in acromegaly.

Main Methods:

  • A cross-sectional study involving 55 acromegalic patients and 65 healthy controls.
  • EPCs were quantified using flow cytometry, assessing markers like KDR, CD34, and CD133.
  • Insulin-like growth factor I (IGF-I) levels were measured by immunoradiometric assay.

Main Results:

  • Acromegalic patients exhibited significantly higher levels of KDR-expressing EPCs compared to controls.
  • Specific subsets, including CD34+KDR+, CD133+KDR+, and CD34+KDR+CD133+ cells, were markedly elevated in acromegaly patients.
  • A strong positive correlation was observed between CD34+KDR+CD133+ cell counts and IGF-I levels in acromegalic patients.

Conclusions:

  • Acromegalic patients demonstrate increased circulating EPCs expressing KDR.
  • These findings suggest a role for IGF-I in modulating EPC differentiation, specifically in the early stages.
  • Elevated EPCs in acromegaly may indicate an adaptive response to altered metabolic and vascular conditions.