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    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2015
    In:  European Journal of Endocrinology Vol. 173, No. 1 ( 2015-07), p. 9-17
    In: European Journal of Endocrinology, Oxford University Press (OUP), Vol. 173, No. 1 ( 2015-07), p. 9-17
    Abstract: Primary hyperparathyroidism (PHPT) has been associated with low-grade inflammation and increased risk of cardiovascular disease (CVD). The aim of the study was to investigate systemic levels of pro-inflammatory proteins that previously have not been examined in patients with PHPT. The selection of the pro-inflammatory biomarkers included in this study, MMP9, S100A4, S100A8/A9 and the receptors sCD14 and RAGE, was based on a previous microarray screen of mRNAs in adipose tissue from PHPT patients. Design A prospective study was conducted on a total of 57 patients with PHPT and a control group of 20 healthy blood donors. Methods PHPT patients with normalisation of serum calcium levels after parathyroidectomy were followed for 6 months. Forty-two patients participated in the longitudinal study, in which blood samples were taken at inclusion, and 1, 3 and 6 months after surgery. Results We observed increased serum levels of MMP9 ( P =0.029), S100A4 ( P 〈 0.001) and sCD14 ( P =0.002) in the 57 patients with PHPT compared to the control-group. During 6 months of follow up, S100A4 ( P =0.022) and sCD14 (0.002) decreased significantly, while serum levels of MMP9 increased ( P =0.025). Conclusions The results demonstrate an increased inflammatory response in PHPT patients shown by elevated MMP9, S100A4 and sCD14 at inclusion. During the 6 months of follow-up, MMP9 increased further, possibly due to the tissue repair process after parathyroidectomy. S100A4 and sCD14 decreased after surgery demonstrating a partial reversal of the systemic inflammation.
    Type of Medium: Online Resource
    ISSN: 0804-4643 , 1479-683X
    RVK:
    Language: Unknown
    Publisher: Oxford University Press (OUP)
    Publication Date: 2015
    detail.hit.zdb_id: 1485160-X
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