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Erschienen in: Pituitary 3/2012

01.09.2012

Procalcitonin can be used as a marker of premature atherosclerosis in acromegaly

verfasst von: H. Ozkan, O. Celik, E. Hatipoglu, F. Kantarci, P. Kadioglu

Erschienen in: Pituitary | Ausgabe 3/2012

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Abstract

The objective of the study was to evaluate arterial morphologic changes of early atherosclerosis and changes in procalcitonin (PCT) levels in patients with acromegaly according to disease activity. Thirty-three active and 20 inactive acromegaly patients followed at Endocrinology-Metabolism out-patient clinic of Cerrahpasa Medical Faculty between 2004 and 2008 were included in the study. Twenty gender and age matched healthy subjects were included as the control group. Intima-media thickness (IMT) of the carotid arteries was measured by ultrasonography. Blood was drawn for biochemical tests and the serum concentrations of C-reactive protein (CRP) and PCT. Intergroup analysis revealed no significant differences between Growth hormone (GH), insulin like growth factor-1 (IGF-1), and IMT (P = 0.42, P = 0.47 respectively). No significant differences were found in the fibrinogen, CRP and PCT levels of the acromegaly patients and the subjects in the control group (P = 0.57, P = 0.84, P = 0.68 respectively). In the patients with IMT ≥ 1 mm, PCT (0.4 [IQR: 0.4–0.55]) levels were significantly different from the patients without atherosclerosis (0.06 [IQR: 0.05–0.12], P < 0.001). The correlation between IMT and PCT (P = 0.001, r = 0.47) was more significant than the correlation between IMT and CRP (P = 0.01, r = 0.28). There was a positive correlation between IMT and atherosclerotic risk factors such as age (P = 0.01, r = 0.27) and body mass index (BMI; P = 0.005, r = 0.32). Our results showed that PCT increases before CRP and it can be useful for the assessment of premature atherosclerosis in acromegaly as well.
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Metadaten
Titel
Procalcitonin can be used as a marker of premature atherosclerosis in acromegaly
verfasst von
H. Ozkan
O. Celik
E. Hatipoglu
F. Kantarci
P. Kadioglu
Publikationsdatum
01.09.2012
Verlag
Springer US
Erschienen in
Pituitary / Ausgabe 3/2012
Print ISSN: 1386-341X
Elektronische ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-011-0327-y

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