Abstract
Normocalcemic primary hyperparathyroidism (NC-PHPT) is a variant of hyperparathyroidism, characterized by normal serum calcium levels, high parathyroid hormone (PTH) and normal 25-OH vitamin D status. The present study aimed to compare complications related to hyperparathyroidism in patients with NC-PHPT and hypercalcemic PHPT (HC-PHPT). We retrospectively evaluated the records of 307 PHPT patients between January 2010 and March 2013. We excluded patients with impaired renal function and liver failure. All patients underwent a biochemical and hormonal examination including serum glucose, albumin, total calcium, phosphorus, creatinine, lipoproteins, PTH and 25-OH vitamin D. Nephrolithiasis and bone mineral density were documented based on a review of the medical records. The study population consisted of 36 (12 %) males and 271 (88 %) females with a mean age of 53.3 ± 9.5 years (29–70 years). Twenty-three of the patients were diagnosed with NC-PHPT (group 1) and 284 were diagnosed with HC-PHPT (group 2). There were no significant differences in terms of age, gender, prevalence of hypertension, low bone mineral density and kidney stones between the groups. The mean thyroid-stimulating hormone (TSH) and low-density lipoprotein (LDL) levels were significantly higher in group 1 than in group 2. Our study found that patients with NC-PHPT have similar several complications as patients with HC-PHPT. NC-PHPT patients have higher TSH levels despite being within the normal range, and higher LDL-C levels than patients with HC-PHPT. However, this relationship needs to be clarified in future studies with larger cohorts.
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References
Yu N, Donnan PT, Murphy MJ, Leese GP (2009) Epidemiology of primary hyperparathyroidism in Tayside, Scotland, UK. Clin Endocrinol 71:485–493
Adami S, Marcocci C, Gatti D (2002) Epidemiology of primary hyperparathyroidism in Europe. J Bone Miner Res 17:18–23
Farahnak P, Larfars G, Sten-Linder M, Nilsson IL (2011) Mild primary hyperparathyroidism: 25-OH Vitamin D deficiency and cardiovascular risk markers. J Clin Endocrinol Metab 96:2112–2118
Wermers RA, Khosla S, Atkinson EJ, Grant CS, Hodgson SF, O’Fallon WM, Melton LJ (1998) Survival after the diagnosis of hyperparathyroidism: a population-based study. Am J Med 104:115–122
Hagstrom E, Lundgren E, Rastad J, Hellman P (2006) Metabolic abnormalities in patients with normocalcemic hyperparathyroidism detected at a population-based screening. Eur J Endocrinol 155:33–39
Ross AC, Taylor CL, Yaktine AL, Del Valle HB (eds) (2011) Dietary reference intakes for calcium and 25-OH vitamin D. The National Academies Press, Washington
Bilezikian JP, Silverberg SJ (2010) Normocalcemic primary hyperparathyroidism. Arq Bras Endocrinol Metabol 54:106–109
Silverberg SJ, Bilezikian JP (2003) Incipient primary hyperparathyroidism: a forme fruste of an old disease. J Clin Endocrinol Metab 88:5348–5352
Cusano NE, Silverberg SJ, Bilezikian JP (2013) Normocalcemic primary hyperparathyroidism. J Clin Densitom 16:33–39
Grant FD, Conlin PR, Brown EM (1990) Rate and concentration dependence of parathyroid hormone dynamics during stepwise changes in serum ionized calcium in normal humans. J Clin Endocrinol Metab 71:370–378
Orwoll E, Blank JB, Barrett-Connor E, Cauley J, Cummings S, Ensrud K, Lewis C, Cawthon PM, Marcus R, Marshall LM, McGowan J, Phipps K, Sherman S, Stefanick ML, Stone K (2005) Design and baseline characteristics of the osteoporotic fractures in men (MrOS) study—a large observational study of the determinants of fracture in older men. Contemp Clin Trials 26:569–585
Lowe H, McMahon DJ, Rubin MR, Bilezikian JP, Silverberg SJ (2007) Normocalcemic primary hyperparathyroidism: further characterization of a new clinical phenotype. J Clin Endocrinol Metab 92:3001–3005
Maruani G, Hertig A, Paillard M, Houillier P (2003) Normocalcemic primary hyperparathyroidism: evidence for a generalized target-tissue resistance to parathyroid hormone. J Clin Endocrinol Metab 88:4641–4648
Tordjman KM, Greenman Y, Osher E, Shenkerman G, Stern N (2004) Characterization of normocalcemic primary hyperparathyroidism. Am J Med 117:861–863
Amaral LM, Queiroz DC, Marques TF, Mendes M, Bandeira F (2012) Normocalcemic versus hypercalcemic primary hyperparathyroidism: more stone than bone? J Osteoporos 3:128352
Cakir I, Unluhizarci K, Tanriverdi F (2012) Investigation of insulin resistance in patients with normocalcemic primary hyperparathyroidism. Endocrine 42:419–422
Gillet C, Bergmann P, Francois D, Body JJ, Corvilain J (1989) Low basal thyrotropin with normal thyroid function in primary hyperparathyroidism. Acta Endocrinol 121:638–642
Ignjatovic VD, Matovic MD, Vukomanovic VR, Jankovic SM, Džodić RR (2013) Is there a link between Hashimoto’s thyroiditis and primary hyperparathyroidism? A study of serum parathormone and anti-TPO antibodies in 2267 patients. Hell J Nucl Med 16:86–90
Hagström E, Lundgren E, Rastad J, Hellman P (2006) Metabolic abnormalities in patients with normocalcemic hyperparathyroidism detected at a population-based screening. Eur J Endocrinol 155:33–39
Temizkan S, Kocak O, Aydin K, Ozderya A, Arslan G, Yucel N, Sargin M (2014) Normocalcemic hyperparathyroidism and insulin resistance. Endocr Pract 6:1–19
Acknowledgments
We thank Prof Alpaslan Kemal Tuzcu from Dicle University School of Medicine for critical review of the manuscript. This research did not receive any specific grant from any funding agency in the public, commercial, or not-for-profit sector.
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The authors declare that there is no conflict of interest that could be perceived as prejudicing the impartiality of the research reported.
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Tuna, M.M., Çalışkan, M., Ünal, M. et al. Normocalcemic hyperparathyroidism is associated with complications similar to those of hypercalcemic hyperparathyroidism. J Bone Miner Metab 34, 331–335 (2016). https://doi.org/10.1007/s00774-015-0673-3
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DOI: https://doi.org/10.1007/s00774-015-0673-3