No effect of surgery on kidney and cardiovascular risk factors in mild primary hyperparathyroidism: secondary analyses from a 10-year randomized controlled trial

Author:

Heck Ansgar1ORCID,Pretorius Mikkel12ORCID,Lundstam Karolina34ORCID,Godang Kristin1ORCID,Hellström Mikael34ORCID,Ueland Thor256ORCID,Bollerslev Jens12ORCID

Affiliation:

1. Section of Specialized Endocrinology, Division of Medicine, Oslo University Hospital , 0424 Oslo , Norway

2. Faculty of Medicine, University of Oslo , 0318 Oslo , Norway

3. Department of Radiology, Institute of Clinical Sciences, The Sahlgrenska Academy, University of Gothenburg , 41685 Gothenburg , Sweden

4. Department of Radiology, Sahlgrenska University Hospital , 41685 Gothenburg , Sweden

5. Research Institute for Internal Medicine, Oslo University Hospital, Rikshospitalet , 0424 Oslo , Norway

6. Thrombosis Research Center (TREC), Division of Internal Medicine, University Hospital of North Norway , 9037 Tromsø , Norway

Abstract

Abstract Objective Renal function and the skeleton are classic target organs in primary hyperparathyroidism (PHPT), affected by the chronic course of the disease. Most patients diagnosed today exhibit mild PHPT, characterized by slight hypercalcemia and no or unspecific symptoms. Concerns have been raised that PHPT could promote deteriorating kidney function and increase cardiovascular risk directly. To examine the effect of parathyroidectomy (PTX) on mild PHPT on renal function and markers for bone turnover, cardiovascular disease (CVD), and vascular inflammation. Design Prospective randomized controlled trial. ClinicalTrials.gov: NCT00522028. Setting Eight Scandinavian referral centers. Participants From 1998 to 2005, 191 patients with mild PHPT were included in Sweden, Norway, and Denmark. Of these 150 were included in the present analyses. Intervention Seventy patients were randomized to PTX and 80 to observation without intervention (OBS). Measures e-GFR was calculated based on creatinine and cystatin C. Markers of CVD and systemic inflammation: osteoprotegerin, vascular cell adhesion molecule 1, soluble CD40 ligand, interleukin-1 receptor antagonist, von Willebrand factor. Bone turnover markers: C-terminal telopeptide of type 1 collagen (CTX-1) and serum Procollagen type 1 N-terminal propeptide. Results No differences in the development of renal function or vascular and systemic inflammation were detected. CTX-1 was lower in PTX after 10 years. Limitations Secondary analyses of a randomized controlled trial. Conclusion PTX does not appear to affect renal function or markers of CVD and vascular inflammation in mild PHPT in a ten-year perspective.

Funder

Swedish government

Norwegian Research Council

South-Eastern Norway Regional Health Authority

Publisher

Oxford University Press (OUP)

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