Influence of Estrogen Therapy on Calcium, Phosphorus, and Other Regulatory Hormones in Postmenopausal Women: The MESA Study

Background: Estrogen therapy (ET) is associated with lower serum calcium and phosphorus concentrations and is known to increase bone mineral density (BMD). Other biomarkers of mineral metabolism may help understand the biological basis of these actions. Methods: We studied 2767 postmenopausal women...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2013-12, Vol.98 (12), p.4890-4898
Hauptverfasser: Bansal, Nisha, Katz, Ronit, de Boer, Ian H, Kestenbaum, Bryan, Siscovick, David S, Hoofnagle, Andrew N, Tracy, Russell, Laughlin, Gail A, Criqui, Michael H, Budoff, Mathew J, Li, Dong, Ix, Joachim H
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container_issue 12
container_start_page 4890
container_title The journal of clinical endocrinology and metabolism
container_volume 98
creator Bansal, Nisha
Katz, Ronit
de Boer, Ian H
Kestenbaum, Bryan
Siscovick, David S
Hoofnagle, Andrew N
Tracy, Russell
Laughlin, Gail A
Criqui, Michael H
Budoff, Mathew J
Li, Dong
Ix, Joachim H
description Background: Estrogen therapy (ET) is associated with lower serum calcium and phosphorus concentrations and is known to increase bone mineral density (BMD). Other biomarkers of mineral metabolism may help understand the biological basis of these actions. Methods: We studied 2767 postmenopausal women in the Multi-Ethnic Study of Atherosclerosis, 862 (31%) of whom were using ET. We measured serum concentrations of calcium, phosphorus, 25-hydroxyvitamin D, 24,25-dihydoxyvitamin D, and fibroblast growth factor-23 and urinary fractional excretion of calcium (FEca) and phosphorus (FEphos). We examined the associations of ET with each biomarker. In addition, we tested whether the adjustment for biomarkers attenuated the association of ET with lumbar BMD measured by abdominal computed tomography in a subset of 810 women. Results: In adjusted models, women who used ET were younger in age [62 (SD 8) vs 66 (9) y, P < .001], had lower mean serum calcium [−13 mg/dL (95% confidence interval [CI] −0.17, −0.10), P < .001] and lower FEca [−0.15% (95% CI −0.21, −0.09), P < .001]. Mean serum phosphorus was lower [−0.19 mg/dL (95% CI −0.23, −0.15), P < .001] and FEphos [0.56% (95% CI 0.16, 0.96), P = .007] was higher in women on ET. Mean 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D were higher [1.52 ng/dL (95% CI 0.57, 2.47), P = .002, and 0.26 ng/mL (95% CI 0.03, 0.48), P = .03, respectively] in women who used ET. Mean PTH and fibroblast growth factor-23 did not differ significantly by the use of ET. ET use was strongly associated with higher lumbar BMD [12.75 mg/cm3 (95% CI 7.77–17.73), P < .001]; however, mineral metabolism measures did not meaningfully alter this association. Conclusions: In a multiethnic cohort of postmenopausal women, ET use was associated with lower serum calcium, lower FEca, lower serum phosphorus, and higher FEphos, suggesting these associations are attributable to increased calcium intake into bone and increased urinary phosphorus excretion. ET use was also associated with greater concentrations of vitamin D metabolites. ET-associated differences in these mineral metabolism measures did not meaningfully attenuate the strong association between ET use and lumbar BMD.
doi_str_mv 10.1210/jc.2013-2286
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Other biomarkers of mineral metabolism may help understand the biological basis of these actions. Methods: We studied 2767 postmenopausal women in the Multi-Ethnic Study of Atherosclerosis, 862 (31%) of whom were using ET. We measured serum concentrations of calcium, phosphorus, 25-hydroxyvitamin D, 24,25-dihydoxyvitamin D, and fibroblast growth factor-23 and urinary fractional excretion of calcium (FEca) and phosphorus (FEphos). We examined the associations of ET with each biomarker. In addition, we tested whether the adjustment for biomarkers attenuated the association of ET with lumbar BMD measured by abdominal computed tomography in a subset of 810 women. Results: In adjusted models, women who used ET were younger in age [62 (SD 8) vs 66 (9) y, P &lt; .001], had lower mean serum calcium [−13 mg/dL (95% confidence interval [CI] −0.17, −0.10), P &lt; .001] and lower FEca [−0.15% (95% CI −0.21, −0.09), P &lt; .001]. Mean serum phosphorus was lower [−0.19 mg/dL (95% CI −0.23, −0.15), P &lt; .001] and FEphos [0.56% (95% CI 0.16, 0.96), P = .007] was higher in women on ET. Mean 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D were higher [1.52 ng/dL (95% CI 0.57, 2.47), P = .002, and 0.26 ng/mL (95% CI 0.03, 0.48), P = .03, respectively] in women who used ET. Mean PTH and fibroblast growth factor-23 did not differ significantly by the use of ET. ET use was strongly associated with higher lumbar BMD [12.75 mg/cm3 (95% CI 7.77–17.73), P &lt; .001]; however, mineral metabolism measures did not meaningfully alter this association. Conclusions: In a multiethnic cohort of postmenopausal women, ET use was associated with lower serum calcium, lower FEca, lower serum phosphorus, and higher FEphos, suggesting these associations are attributable to increased calcium intake into bone and increased urinary phosphorus excretion. ET use was also associated with greater concentrations of vitamin D metabolites. ET-associated differences in these mineral metabolism measures did not meaningfully attenuate the strong association between ET use and lumbar BMD.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jc.2013-2286</identifier><identifier>PMID: 24092825</identifier><identifier>CODEN: JCEMAZ</identifier><language>eng</language><publisher>Bethesda, MD: Endocrine Society</publisher><subject>24,25-Dihydroxyvitamin D 3 - blood ; 24,25-Dihydroxyvitamin D 3 - metabolism ; 25-Hydroxyvitamin D 2 - blood ; 25-Hydroxyvitamin D 2 - metabolism ; Aged ; Aged, 80 and over ; Biological and medical sciences ; Biomarkers - blood ; Biomarkers - metabolism ; Biomarkers - urine ; Bone and Bones - diagnostic imaging ; Bone and Bones - drug effects ; Bone and Bones - metabolism ; Bone Density - drug effects ; Calcifediol - blood ; Calcifediol - metabolism ; Calcium - blood ; Calcium - urine ; Cohort Studies ; Cross-Sectional Studies ; Endocrine Research ; Endocrinopathies ; Ergocalciferols - blood ; Ergocalciferols - metabolism ; Estrogen Replacement Therapy ; Feeding. Feeding behavior ; Female ; Fibroblast Growth Factors - blood ; Fundamental and applied biological sciences. Psychology ; Humans ; Medical sciences ; Middle Aged ; Osteoporosis, Postmenopausal - blood ; Osteoporosis, Postmenopausal - diagnostic imaging ; Osteoporosis, Postmenopausal - metabolism ; Osteoporosis, Postmenopausal - prevention &amp; control ; Phosphorus - blood ; Phosphorus - urine ; Radiography ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Vertebrates: endocrinology ; Vitamin D - analogs &amp; derivatives ; Vitamin D - blood ; Vitamin D - metabolism</subject><ispartof>The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.4890-4898</ispartof><rights>Copyright © 2013 by The Endocrine Society</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 by The Endocrine Society 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6023-ff49346158b14e1ef7c58024305f4ac623868eb078fbe8e53ff5f092065c4cd43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28032637$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24092825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bansal, Nisha</creatorcontrib><creatorcontrib>Katz, Ronit</creatorcontrib><creatorcontrib>de Boer, Ian H</creatorcontrib><creatorcontrib>Kestenbaum, Bryan</creatorcontrib><creatorcontrib>Siscovick, David S</creatorcontrib><creatorcontrib>Hoofnagle, Andrew N</creatorcontrib><creatorcontrib>Tracy, Russell</creatorcontrib><creatorcontrib>Laughlin, Gail A</creatorcontrib><creatorcontrib>Criqui, Michael H</creatorcontrib><creatorcontrib>Budoff, Mathew J</creatorcontrib><creatorcontrib>Li, Dong</creatorcontrib><creatorcontrib>Ix, Joachim H</creatorcontrib><title>Influence of Estrogen Therapy on Calcium, Phosphorus, and Other Regulatory Hormones in Postmenopausal Women: The MESA Study</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>Background: Estrogen therapy (ET) is associated with lower serum calcium and phosphorus concentrations and is known to increase bone mineral density (BMD). Other biomarkers of mineral metabolism may help understand the biological basis of these actions. Methods: We studied 2767 postmenopausal women in the Multi-Ethnic Study of Atherosclerosis, 862 (31%) of whom were using ET. We measured serum concentrations of calcium, phosphorus, 25-hydroxyvitamin D, 24,25-dihydoxyvitamin D, and fibroblast growth factor-23 and urinary fractional excretion of calcium (FEca) and phosphorus (FEphos). We examined the associations of ET with each biomarker. In addition, we tested whether the adjustment for biomarkers attenuated the association of ET with lumbar BMD measured by abdominal computed tomography in a subset of 810 women. Results: In adjusted models, women who used ET were younger in age [62 (SD 8) vs 66 (9) y, P &lt; .001], had lower mean serum calcium [−13 mg/dL (95% confidence interval [CI] −0.17, −0.10), P &lt; .001] and lower FEca [−0.15% (95% CI −0.21, −0.09), P &lt; .001]. Mean serum phosphorus was lower [−0.19 mg/dL (95% CI −0.23, −0.15), P &lt; .001] and FEphos [0.56% (95% CI 0.16, 0.96), P = .007] was higher in women on ET. Mean 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D were higher [1.52 ng/dL (95% CI 0.57, 2.47), P = .002, and 0.26 ng/mL (95% CI 0.03, 0.48), P = .03, respectively] in women who used ET. Mean PTH and fibroblast growth factor-23 did not differ significantly by the use of ET. ET use was strongly associated with higher lumbar BMD [12.75 mg/cm3 (95% CI 7.77–17.73), P &lt; .001]; however, mineral metabolism measures did not meaningfully alter this association. Conclusions: In a multiethnic cohort of postmenopausal women, ET use was associated with lower serum calcium, lower FEca, lower serum phosphorus, and higher FEphos, suggesting these associations are attributable to increased calcium intake into bone and increased urinary phosphorus excretion. ET use was also associated with greater concentrations of vitamin D metabolites. ET-associated differences in these mineral metabolism measures did not meaningfully attenuate the strong association between ET use and lumbar BMD.</description><subject>24,25-Dihydroxyvitamin D 3 - blood</subject><subject>24,25-Dihydroxyvitamin D 3 - metabolism</subject><subject>25-Hydroxyvitamin D 2 - blood</subject><subject>25-Hydroxyvitamin D 2 - metabolism</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - metabolism</subject><subject>Biomarkers - urine</subject><subject>Bone and Bones - diagnostic imaging</subject><subject>Bone and Bones - drug effects</subject><subject>Bone and Bones - metabolism</subject><subject>Bone Density - drug effects</subject><subject>Calcifediol - blood</subject><subject>Calcifediol - metabolism</subject><subject>Calcium - blood</subject><subject>Calcium - urine</subject><subject>Cohort Studies</subject><subject>Cross-Sectional Studies</subject><subject>Endocrine Research</subject><subject>Endocrinopathies</subject><subject>Ergocalciferols - blood</subject><subject>Ergocalciferols - metabolism</subject><subject>Estrogen Replacement Therapy</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fibroblast Growth Factors - blood</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Osteoporosis, Postmenopausal - blood</subject><subject>Osteoporosis, Postmenopausal - diagnostic imaging</subject><subject>Osteoporosis, Postmenopausal - metabolism</subject><subject>Osteoporosis, Postmenopausal - prevention &amp; control</subject><subject>Phosphorus - blood</subject><subject>Phosphorus - urine</subject><subject>Radiography</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Vertebrates: endocrinology</subject><subject>Vitamin D - analogs &amp; derivatives</subject><subject>Vitamin D - blood</subject><subject>Vitamin D - metabolism</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd9rFDEQxxdR7Fl981nyIvhwW_Nrd7M-COW42kKlxVb0LeRyk9s9s8ma7LYc_vNmubMqCIaBMMlnvjPDN8teEnxCKMFvt_qEYsJySkX5KJuRmhd5RerqcTbDmJK8rujXo-xZjFuMCecFe5odUY5rKmgxy35cOGNHcBqQN2gZh-A34NBtA0H1O-QdWiir27Gbo-vGx77xYYxzpNwaXQ0JQp9gM1o1-LBD5z503kFErUPXPg4dON-rMSqLvviUvJtk0cflzSm6Gcb17nn2xCgb4cXhPs4-ny1vF-f55dWHi8XpZa5LTFluDK8ZL0khVoQDAVPpQmDKGS4MV7qkTJQCVrgSZgUCCmZMYdJ-uCw012vOjrP3e91-XHWw1uCGoKzsQ9upsJNetfLvH9c2cuPvJBO8LgVOAm8OAsF_HyEOsmujBmuVAz9GSUqSQhSC_h_lZSFSiDqh8z2qg48xgHmYiGA5WSu3Wk7WysnahL_6c4sH-JeXCXh9AFTUypqgnG7jby4tQktWJY7vuXtvBwjxmx3vIcgGlB0aidPhZSXyqTOhKcunF5bK2L4M3Nrr0DroA8Qot34MLtn376l_AqGnzUE</recordid><startdate>201312</startdate><enddate>201312</enddate><creator>Bansal, Nisha</creator><creator>Katz, Ronit</creator><creator>de Boer, Ian H</creator><creator>Kestenbaum, Bryan</creator><creator>Siscovick, David S</creator><creator>Hoofnagle, Andrew N</creator><creator>Tracy, Russell</creator><creator>Laughlin, Gail A</creator><creator>Criqui, Michael H</creator><creator>Budoff, Mathew J</creator><creator>Li, Dong</creator><creator>Ix, Joachim H</creator><general>Endocrine Society</general><general>Copyright by The Endocrine Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QP</scope><scope>5PM</scope></search><sort><creationdate>201312</creationdate><title>Influence of Estrogen Therapy on Calcium, Phosphorus, and Other Regulatory Hormones in Postmenopausal Women: The MESA Study</title><author>Bansal, Nisha ; Katz, Ronit ; de Boer, Ian H ; Kestenbaum, Bryan ; Siscovick, David S ; Hoofnagle, Andrew N ; Tracy, Russell ; Laughlin, Gail A ; Criqui, Michael H ; Budoff, Mathew J ; Li, Dong ; Ix, Joachim H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6023-ff49346158b14e1ef7c58024305f4ac623868eb078fbe8e53ff5f092065c4cd43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>24,25-Dihydroxyvitamin D 3 - blood</topic><topic>24,25-Dihydroxyvitamin D 3 - metabolism</topic><topic>25-Hydroxyvitamin D 2 - blood</topic><topic>25-Hydroxyvitamin D 2 - metabolism</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - metabolism</topic><topic>Biomarkers - urine</topic><topic>Bone and Bones - diagnostic imaging</topic><topic>Bone and Bones - drug effects</topic><topic>Bone and Bones - metabolism</topic><topic>Bone Density - drug effects</topic><topic>Calcifediol - blood</topic><topic>Calcifediol - metabolism</topic><topic>Calcium - blood</topic><topic>Calcium - urine</topic><topic>Cohort Studies</topic><topic>Cross-Sectional Studies</topic><topic>Endocrine Research</topic><topic>Endocrinopathies</topic><topic>Ergocalciferols - blood</topic><topic>Ergocalciferols - metabolism</topic><topic>Estrogen Replacement Therapy</topic><topic>Feeding. 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Psychology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Osteoporosis, Postmenopausal - blood</topic><topic>Osteoporosis, Postmenopausal - diagnostic imaging</topic><topic>Osteoporosis, Postmenopausal - metabolism</topic><topic>Osteoporosis, Postmenopausal - prevention &amp; control</topic><topic>Phosphorus - blood</topic><topic>Phosphorus - urine</topic><topic>Radiography</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Vertebrates: endocrinology</topic><topic>Vitamin D - analogs &amp; derivatives</topic><topic>Vitamin D - blood</topic><topic>Vitamin D - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bansal, Nisha</creatorcontrib><creatorcontrib>Katz, Ronit</creatorcontrib><creatorcontrib>de Boer, Ian H</creatorcontrib><creatorcontrib>Kestenbaum, Bryan</creatorcontrib><creatorcontrib>Siscovick, David S</creatorcontrib><creatorcontrib>Hoofnagle, Andrew N</creatorcontrib><creatorcontrib>Tracy, Russell</creatorcontrib><creatorcontrib>Laughlin, Gail A</creatorcontrib><creatorcontrib>Criqui, Michael H</creatorcontrib><creatorcontrib>Budoff, Mathew J</creatorcontrib><creatorcontrib>Li, Dong</creatorcontrib><creatorcontrib>Ix, Joachim H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bansal, Nisha</au><au>Katz, Ronit</au><au>de Boer, Ian H</au><au>Kestenbaum, Bryan</au><au>Siscovick, David S</au><au>Hoofnagle, Andrew N</au><au>Tracy, Russell</au><au>Laughlin, Gail A</au><au>Criqui, Michael H</au><au>Budoff, Mathew J</au><au>Li, Dong</au><au>Ix, Joachim H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Estrogen Therapy on Calcium, Phosphorus, and Other Regulatory Hormones in Postmenopausal Women: The MESA Study</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2013-12</date><risdate>2013</risdate><volume>98</volume><issue>12</issue><spage>4890</spage><epage>4898</epage><pages>4890-4898</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><abstract>Background: Estrogen therapy (ET) is associated with lower serum calcium and phosphorus concentrations and is known to increase bone mineral density (BMD). Other biomarkers of mineral metabolism may help understand the biological basis of these actions. Methods: We studied 2767 postmenopausal women in the Multi-Ethnic Study of Atherosclerosis, 862 (31%) of whom were using ET. We measured serum concentrations of calcium, phosphorus, 25-hydroxyvitamin D, 24,25-dihydoxyvitamin D, and fibroblast growth factor-23 and urinary fractional excretion of calcium (FEca) and phosphorus (FEphos). We examined the associations of ET with each biomarker. In addition, we tested whether the adjustment for biomarkers attenuated the association of ET with lumbar BMD measured by abdominal computed tomography in a subset of 810 women. Results: In adjusted models, women who used ET were younger in age [62 (SD 8) vs 66 (9) y, P &lt; .001], had lower mean serum calcium [−13 mg/dL (95% confidence interval [CI] −0.17, −0.10), P &lt; .001] and lower FEca [−0.15% (95% CI −0.21, −0.09), P &lt; .001]. Mean serum phosphorus was lower [−0.19 mg/dL (95% CI −0.23, −0.15), P &lt; .001] and FEphos [0.56% (95% CI 0.16, 0.96), P = .007] was higher in women on ET. Mean 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D were higher [1.52 ng/dL (95% CI 0.57, 2.47), P = .002, and 0.26 ng/mL (95% CI 0.03, 0.48), P = .03, respectively] in women who used ET. Mean PTH and fibroblast growth factor-23 did not differ significantly by the use of ET. ET use was strongly associated with higher lumbar BMD [12.75 mg/cm3 (95% CI 7.77–17.73), P &lt; .001]; however, mineral metabolism measures did not meaningfully alter this association. Conclusions: In a multiethnic cohort of postmenopausal women, ET use was associated with lower serum calcium, lower FEca, lower serum phosphorus, and higher FEphos, suggesting these associations are attributable to increased calcium intake into bone and increased urinary phosphorus excretion. ET use was also associated with greater concentrations of vitamin D metabolites. ET-associated differences in these mineral metabolism measures did not meaningfully attenuate the strong association between ET use and lumbar BMD.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>24092825</pmid><doi>10.1210/jc.2013-2286</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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ispartof The journal of clinical endocrinology and metabolism, 2013-12, Vol.98 (12), p.4890-4898
issn 0021-972X
1945-7197
language eng
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source MEDLINE; Journals@Ovid Complete; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects 24,25-Dihydroxyvitamin D 3 - blood
24,25-Dihydroxyvitamin D 3 - metabolism
25-Hydroxyvitamin D 2 - blood
25-Hydroxyvitamin D 2 - metabolism
Aged
Aged, 80 and over
Biological and medical sciences
Biomarkers - blood
Biomarkers - metabolism
Biomarkers - urine
Bone and Bones - diagnostic imaging
Bone and Bones - drug effects
Bone and Bones - metabolism
Bone Density - drug effects
Calcifediol - blood
Calcifediol - metabolism
Calcium - blood
Calcium - urine
Cohort Studies
Cross-Sectional Studies
Endocrine Research
Endocrinopathies
Ergocalciferols - blood
Ergocalciferols - metabolism
Estrogen Replacement Therapy
Feeding. Feeding behavior
Female
Fibroblast Growth Factors - blood
Fundamental and applied biological sciences. Psychology
Humans
Medical sciences
Middle Aged
Osteoporosis, Postmenopausal - blood
Osteoporosis, Postmenopausal - diagnostic imaging
Osteoporosis, Postmenopausal - metabolism
Osteoporosis, Postmenopausal - prevention & control
Phosphorus - blood
Phosphorus - urine
Radiography
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Vertebrates: endocrinology
Vitamin D - analogs & derivatives
Vitamin D - blood
Vitamin D - metabolism
title Influence of Estrogen Therapy on Calcium, Phosphorus, and Other Regulatory Hormones in Postmenopausal Women: The MESA Study
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