Horm Metab Res 2013; 45(04): 314-318
DOI: 10.1055/s-0032-1323765
Humans, Clinical
© Georg Thieme Verlag KG Stuttgart · New York

Oxidative Stress and Reduced Antioxidative Status, along with Endothelial Dysfunction in Acromegaly

Authors

  • P. Anagnostis

    1   Department of Endocrinology, “Hippokration” General Hospital of Thessaloniki, Thessaloniki, Greece
  • Z. A. Efstathiadou

    1   Department of Endocrinology, “Hippokration” General Hospital of Thessaloniki, Thessaloniki, Greece
  • S. Gougoura

    2   Endocrinology and Metabolic Diseases Research Laboratory, School of Medicine, University of Thessaly, Biopolis, Larissa, Greece
  • S. A. Polyzos

    3   Second Medical Clinic, Medical School, Aristotle University of Thessaloniki, Ippokration Hospital, Thessaloniki, Greece
  • E. Karathanasi

    1   Department of Endocrinology, “Hippokration” General Hospital of Thessaloniki, Thessaloniki, Greece
  • P. Dritsa

    2   Endocrinology and Metabolic Diseases Research Laboratory, School of Medicine, University of Thessaly, Biopolis, Larissa, Greece
  • M. Kita

    1   Department of Endocrinology, “Hippokration” General Hospital of Thessaloniki, Thessaloniki, Greece
  • G. N. Koukoulis

    2   Endocrinology and Metabolic Diseases Research Laboratory, School of Medicine, University of Thessaly, Biopolis, Larissa, Greece
Further Information

Publication History

received 23 March 2012

accepted 14 August 2012

Publication Date:
23 October 2012 (online)

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Abstract

Acromegaly is characterized by high cardiovascular morbidity and mortality. Oxidative stress and endothelial dysfunction are underlying mechanisms of atherosclerosis.The aim of this study was to evaluate the blood redox status and endothelial function by means of nitric oxide (NO) levels in patients with acromegaly. Total antioxidant capacity (TAC), catalase activity and glutathione concentration (GSH), as measures of antioxidative capacity, total oxidized glutathione (GSSG) and thiobarbituric acid reactive substances (TBARS), as indices of oxidative stress, and NO levels were assessed in 15 patients with acromegaly (age 55.4±10.5 years; 6 males) and 15 age- and sex-matched controls (age 58.4±8.1 years; 7 males). Active disease was present in 12 patients: 11 on current pharmacotherapy and 1 newly diagnosed. Three acromegalics were in remission after successful treatment. Acromegalics as compared with controls had significantly lower levels of catalase activity (8.2±5.8 vs. 51.3±29.1 mmol/ml/min, p<0.001), GSH (0.97±0.54 vs. 1.41±0.35 mmol/l, p=0.006), GSSG (0.27±0.19 vs. 2.04±1.32 mmol/l, p=0.002) and NO levels (6.0±3.1 vs. 43.0±29.8 mmol/l, p<0.001), but higher TBARS (16.3±8.9 vs. 10.1±10.8, nmol/ml, p=0.019). After adjustment for confounders, differences in catalase activity, NO levels and TBARS remained significant (p=0.004, p<0.001 and p=0.025, respectively). No association between IGF-I/GH and oxidative stress markers was noticed, except for a positive correlation between nadir GH and GSSG (r2=0.563, p=0.036). Acromegaly is associated with increased levels of oxidative stress coupled by diminished antioxidant capacity and endothelial dysfunction indicated by the presence of decreased NO levels.