Literature DB >> 20519351

Left-shifted relation between calcium and parathyroid hormone in obesity.

Hella Hultin1, Katarina Edfeldt, Magnus Sundbom, Per Hellman.   

Abstract

BACKGROUND: A condition resembling secondary hyperparathyroidism (HPT), including raised levels of PTH and normal levels of serum calcium, has been reported in obesity. A plausible reason may be vitamin D deficiency, but conflicting data have been reported.
OBJECTIVE: Our objective was to investigate calcium homeostasis in obese individuals with emphasis on the function of the parathyroid glands. DESIGN AND INTERVENTION: Morbidly obese patients (mean body mass index=46.6+/-6) were examined for their status of calcium homeostasis. A subset was thoroughly investigated with calcium-citrate (CiCa) clamping. PATIENTS: Of 108 morbidly obese patients, 11 underwent CiCa clamping as well as 21 healthy volunteers of normal weight and 15 with primary HPT (pHPT). Large patient cohorts of normal individuals and pHPT patients were also used as comparisons. OUTCOME MEASURES AND
RESULTS: All obese individuals had normal serum calcium and creatinine levels. Mean levels of 25-OH-vitamin D3 in serum were low, 53 nmol/liter (reference range 75-250 nmol/liter). Mean intact plasma PTH was 5.1 pmol/liter (reference range 1.1-6.9 pmol/liter). There was a significant positive correlation between PTH and duration of obesity. CiCa clamping in obese subjects revealed a remarkably high sensitivity for calcium and a left-shifted relation between plasma calcium and PTH (set point) compared with the normal population. CiCa clamping in pHPT patients demonstrated a right-shifted PTH-Ca curve.
CONCLUSION: Although vitamin D levels in the obese individuals were low, few displayed overt signs of secondary HPT. The CiCa clamping implied a disturbance in the calcium homeostasis comparable to early renal insufficiency, with a left-shifted Ca-PTH curve and a lower set point compared with the normal population.

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Year:  2010        PMID: 20519351     DOI: 10.1210/jc.2009-2822

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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