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      Effect of vitamin D nutrition on disease indices in patients with primary hyperparathyroidism.

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          Abstract

          In patients with primary hyperparathyroidism, the size of the adenoma is a major determinant of biochemical indices, disease severity, and manner of presentation. However, the large variation in adenoma weight, both within and between populations and a steady decline in parathyroid adenoma weights over time remain largely unexplained. Based on the results in a small number of patients almost two decades ago we proposed that vitamin D nutritional status of the patient explains both the disease manifestations and much of the variation in adenoma size. Accordingly, we examined the relationship between vitamin D nutrition, as assessed by serum levels of 25-hydroxyvitamin D, and parathyroid gland weight, the best available index of disease severity, in a large number of patients (n = 440) with primary hyperparathyroidism. A significant inverse relationship was found between serum 25-hydroxyvitamin D level and log adenoma weight (r = -0.361; p < 0.001). Also, the adenoma weight was significantly related directly to serum PTH, calcium, and alkaline phosphatase as dependent variables. In patients with vitamin D deficiency (defined as serum 25-hydroxyvitamin D levels 15 ng/mL or lower), gland weight, PTH, AP, and adjusted calcium were each significantly higher than in patients with 25-hydroxyvitamin D levels of 16 ng/mL or higher, but serum 1,25-dihydroxyvitamin D levels were similar in both groups. We interpret this to mean that suboptimal vitamin D nutrition stimulates parathyroid adenoma growth by a mechanism unrelated to 1,25-dihydroxyvitamin D deficiency. We conclude that variable vitamin D nutritional status in the population may partly explain the differences in disease presentation.

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          Author and article information

          Journal
          J Steroid Biochem Mol Biol
          The Journal of steroid biochemistry and molecular biology
          Elsevier BV
          1879-1220
          0960-0760
          July 2020
          : 201
          Affiliations
          [1 ] Division of Endocrinology, Diabetes, and Bone & Mineral Disorders, Department of Internal Medicine, Henry Ford Hospital, 3031 W. Grand Blvd, Suite # 800, Detroit, MI 48202, United States; Bone & Mineral Research Laboratory, Henry Ford Health System/Wayne State University Integrative Biosciences (IBio) Research Building, 6135 Woodward Avenue, Detroit, MI 48202, United States. Electronic address: srao1@hfhs.org.
          [2 ] Division of Endocrinology, Diabetes, and Bone & Mineral Disorders, Department of Internal Medicine, Henry Ford Hospital, 3031 W. Grand Blvd, Suite # 800, Detroit, MI 48202, United States.
          [3 ] Bone & Mineral Research Laboratory, Henry Ford Health System/Wayne State University Integrative Biosciences (IBio) Research Building, 6135 Woodward Avenue, Detroit, MI 48202, United States.
          [4 ] Department of Public Helath Sciences Henry Ford Health System One Ford Place Detroit, MI 48202, United States.
          Article
          S0960-0760(19)30549-7
          10.1016/j.jsbmb.2020.105695
          32407867
          8b2fc7f1-16ec-437c-a648-616e4aab7a3a
          History

          25-Hydroxyvitamin D,Parathyroid gland weight,Parathyroid hormone,Primary hyperparathyroidism,Vitamin D nutrition

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