Vitamin D, Calcium, Parathyroid Hormone, and Sex Steroids in Bone Health and Effects of Aging

被引:80
作者
Bhattarai, Hitesh Kumar [1 ]
Shrestha, Shreya [1 ]
Rokka, Kabita [1 ]
Shakya, Rosy [1 ]
机构
[1] Kathmandu Univ, Dept Biotechnol, Dhulikhel, Nepal
关键词
AGE-RELATED-CHANGES; MINERAL DENSITY; TRABECULAR BONE; D-RECEPTOR; POSTMENOPAUSAL WOMEN; NORMAL YOUNG; ESTROGEN; OSTEOPOROSIS; ABSORPTION; MECHANISMS;
D O I
10.1155/2020/9324505
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Bone health of the elderly is a major global health concern, since about 1 in 3 women and 1 in 5 men suffer from bone loss and fractures, often called osteoporosis, in old age. Bone health is a complex issue affected by multiple hormones and minerals. Among all the hormones involved in bone health, calcitriol (also vitamin D), parathyroid, and sex hormones (especially estrogen) have been discussed in this review paper. We have discussed the metabolism of these hormones and their effects on bone health. Vitamin D can be obtained from diet or formed from 7-dehydrocholesterol found under the skin in the presence of sunlight. The active form, calcitriol, causes dimerization of vitamin D receptor and acts on the bones, intestine, and kidney to regulate the level of calcium in blood. Similarly, parathyroid hormone is secreted when the serum level of calcium is low. It helps regulate the level of blood calcium through calcitriol. Sex hormones regulate bone modeling at an early age and remodeling later in life. Loss of ovarian function and a decrement in the level of production of estrogen are marked by bone loss in elderly women. In the elderly, various changes in the calcium and vitamin D metabolism, such as decrease in the production of vitamin D, decrease in dietary vitamin D, decreased renal production, increased production of excretory products, decrease in the level of VDR, and decreased calcium absorption by the intestines, can lead to bone loss. When the elderly are diagnosed with osteoporosis, medications that directly target bone such as bisphosphonates, RANK ligand inhibitors, estrogen and estrogen analogues, estrogen receptor modulators, and parathyroid hormone receptor agonists are used. Additionally, calcium and vitamin D supplements are prescribed.
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页数:10
相关论文
共 59 条
[21]   A systematic review of intervention thresholds based on FRAX A report prepared for the National Osteoporosis Guideline Group and the International Osteoporosis Foundation [J].
Kanis, John A. ;
Harvey, Nicholas C. ;
Cooper, Cyrus ;
Johansson, Helena ;
Oden, Anders ;
McCloskey, Eugene V. .
ARCHIVES OF OSTEOPOROSIS, 2016, 11 (01)
[22]   Relationship of serum sex steroid levels and bone turnover markers with bone mineral density in men and women: A key role for bioavailable estrogen [J].
Khosla, S ;
Melton, LJ ;
Atkinson, EJ ;
O'Fallon, WM ;
Klee, GG ;
Riggs, BL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (07) :2266-2274
[23]   Association between intestinal vitamin D receptor, calcium absorption, and serum 1,25 dihydroxyvitamin D in normal young and elderly women [J].
Kinyamu, HK ;
Gallagher, JC ;
Prahl, JM ;
Deluca, HF ;
Petranick, KM ;
Lanspa, SJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (06) :922-928
[24]   Serum vitamin D metabolites and calcium absorption in normal young and elderly free-living women and in women living in nursing homes [J].
Kinyamu, HK ;
Gallagher, JC ;
Balhorn, KE ;
Petranick, KM ;
Rafferty, KA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1997, 65 (03) :790-797
[25]   Ovariectomy disregulates osteoblast and osteoclast formation through the T-cell receptor CD40 ligand [J].
Li, Jau-Yi ;
Tawfeek, Hesham ;
Bedi, Brahmchetna ;
Yang, Xiaoying ;
Adams, Jonathan ;
Gao, Kristy Y. ;
Zayzafoon, Majd ;
Weitzmann, M. Neale ;
Pacifici, Roberto .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (02) :768-773
[26]  
LINDSAY R, 1976, LANCET, V1, P1038
[27]   Vitamin D physiology [J].
Lips, P. .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2006, 92 (01) :4-8
[28]  
Lips P., 2014, BONE ABSTRACTS, V3, P1014, DOI [10.1530/boneabs.3.ahp4, DOI 10.1530/BONEABS.3.AHP4]
[29]   Estrogen enhances the functions of CD4+CD25+Foxp3+ regulatory T cells that suppress osteoclast differentiation and bone resorption in vitro [J].
Luo, C. Y. ;
Wang, L. ;
Sun, C. ;
Li, D. J. .
CELLULAR & MOLECULAR IMMUNOLOGY, 2011, 8 (01) :50-58
[30]  
Maclaughlin J., 1986, Nutr Clin Pract, V1, P57, DOI [10.1177/088453368600100118, DOI 10.1177/088453368600100118]