Sporadic and MEN1‐Related Primary Hyperparathyroidism: Differences in Clinical Expression and Severity |
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Authors: | Cristina Eller‐Vainicher Iacopo Chiodini Claudia Battista Raffaella Viti Maria Lucia Mascia Sara Massironi Maddalena Peracchi Leonardo D'Agruma Salvatore Minisola Sabrina Corbetta David EC Cole Anna Spada Alfredo Scillitani |
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Affiliation: | 1. Unit of Endocrinology‐Diabetology, Department of Medical Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, IRCCS, Milan, Italy;2. Unit of Endocrinology, “Casa Sollievo della Sofferenza,” IRCCS, San Giovanni Rotondo, Foggia, Italy;3. Department of Clinical Sciences, University “La Sapienza,” University of Rome, Rome, Italy;4. Unit of Gastroenterology, Department of Medical Sciences, University of Milan, Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, IRCCS, Milan, Italy;5. Unit of Genetics, “Casa Sollievo della Sofferenza,” IRCCS, San Giovanni Rotondo, Foggia, Italy;6. Unit of Endocrinology, Department of Medical and Surgical Sciences, University of Milan, IRCCS Policlinico San Donato Institute, San Donato Milanese, Milan, Italy;7. Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada |
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Abstract: | Primary hyperparathyroidism (PHPT) is a common endocrine disease that is associated with multiple endocrine neoplasia type 1 (MEN1) in ~2% of PHPT cases. Lack of a family history and other specific expressions may lead to underestimated MEN1 prevalence in PHPT. The aim of this study was to identify clinical or biochemical features predictive of MEN1 and to compare the severity of the disease in MEN1‐related versus sporadic PHPT (sPHPT). We performed a 36‐mo cross‐sectional observational study in three tertiary referral centers on an outpatient basis on 469 consecutive patients with sporadic PHPT and 64 with MEN1‐related PHPT. Serum calcium, phosphate, PTH, 25(OH)D3, and creatinine clearance were measured, and ultrasound examination of the urinary tract/urography was performed in all patients. In 432 patients, BMD was measured at the lumbar spine (LS) and femoral neck (FN). MEN1 patients showed lower BMD Z‐scores at the LS (?1.33 ± 1.23 versus ?0.74 ± 1.4, p = 0.008) and FN (?1.13 ± 0.96 versus ?0.6 ± 1.07, p = 0.002) and lower phosphate (2.38 ± 0.52 versus 2.56 ± 0.45 mg/dl, p = 0.003) and PTH (113.8 ± 69.5 versus 173.7 ± 135 pg/ml, p = 0.001) levels than sPHPT patients. Considering probands only, the presence of MEN1 was more frequently associated with PTH values in the normal range (OR, 3.01; 95% CI, 1.07–8.50; p = 0.037) and younger age (OR, 1.61; 95% CI, 1.28–2.02; p = 0.0001). A combination of PTH values in the normal range plus age <50 yr was strongly associated with MEN1 presence (OR, 13.51; 95% CI, 3.62–50.00; p = 0.0001). In conclusion, MEN1‐related PHPT patients show more severe bone but similar kidney involvement despite a milder biochemical presentation compared with their sPHPT counterparts. Normal PTH levels and young age are associated with MEN1 presence. |
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Keywords: | parathyroid familial hyperparathyroidism PTH multiple endocrine neoplasia type 1 hypercalcemia |
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