Bone Disease in Renal Transplantation and Pleotropic Effects of Vitamin D Therapy
Abstract Osteoporosis, osteopenia, and osteonecrosis are common in renal transplant recipients. In this study, we evaluated relationship between bone mineral density (BMD) and posttransplant duration; creatinine clearance; serum levels of glucose, calcium, phosphorus, alkaline phosphatase, vitamin D...
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description | Abstract Osteoporosis, osteopenia, and osteonecrosis are common in renal transplant recipients. In this study, we evaluated relationship between bone mineral density (BMD) and posttransplant duration; creatinine clearance; serum levels of glucose, calcium, phosphorus, alkaline phosphatase, vitamin D (vitD), parathormone, magnesium, C telopeptide, osteocalcin, lipids, and vit D therapy. Eighty five subjects included in this study had a mean age of 36.25 ± 10.5 years. At least at 6-month intervals we measured femoral neck (FN) and lumbar vertebra (LV) by DEXA and biochemical parameters. VitD was prescribed in 57 patients (vitDG). The mean duration of posttransplantation follow-up was 9.82 ± 2.72 months. T scores (TS) of FN and LV were normal in 29.4% and 21.2%; osteopenia in 56.5% and 49.4%; and osteoporosis in 12.1% and 29.4% of patients, respectively. Upon follow-up, TS improved significantly from −1.58 to −1.46 in FN and from −1.88 to −1.70 in LV ( P < .05 for both). In patients receiving vitDG, TS improved significantly from −1.74 to −1.61 on FN and from −2.16 to −1.97 on LV ( P < .05 for both). Osteocalcin and vitDG levels decreased in all patients ( P < .05 for all). Blood urea nitrogen and serum creatinine increased ( P < .05). In VitDG cohort, triglyceride levels decreased ( P < .05) with unchanged blood glucose values; but among the other patients, triglycerides were unchanged but glucose levels had increased ( P < .05). Bone disease including osteopenia or osteoporosis was observed among 70%. During the follow-up period, BMD increased significantly from baseline at 9.82 ± 2.72 months. VitD therapy caused more prominent improvements in BMD and decreases in serum triglycerides as well as mutigated the increase in blood glucose. |
doi_str_mv | 10.1016/j.transproceed.2010.04.054 |
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In this study, we evaluated relationship between bone mineral density (BMD) and posttransplant duration; creatinine clearance; serum levels of glucose, calcium, phosphorus, alkaline phosphatase, vitamin D (vitD), parathormone, magnesium, C telopeptide, osteocalcin, lipids, and vit D therapy. Eighty five subjects included in this study had a mean age of 36.25 ± 10.5 years. At least at 6-month intervals we measured femoral neck (FN) and lumbar vertebra (LV) by DEXA and biochemical parameters. VitD was prescribed in 57 patients (vitDG). The mean duration of posttransplantation follow-up was 9.82 ± 2.72 months. T scores (TS) of FN and LV were normal in 29.4% and 21.2%; osteopenia in 56.5% and 49.4%; and osteoporosis in 12.1% and 29.4% of patients, respectively. Upon follow-up, TS improved significantly from −1.58 to −1.46 in FN and from −1.88 to −1.70 in LV ( P < .05 for both). In patients receiving vitDG, TS improved significantly from −1.74 to −1.61 on FN and from −2.16 to −1.97 on LV ( P < .05 for both). Osteocalcin and vitDG levels decreased in all patients ( P < .05 for all). Blood urea nitrogen and serum creatinine increased ( P < .05). In VitDG cohort, triglyceride levels decreased ( P < .05) with unchanged blood glucose values; but among the other patients, triglycerides were unchanged but glucose levels had increased ( P < .05). Bone disease including osteopenia or osteoporosis was observed among 70%. During the follow-up period, BMD increased significantly from baseline at 9.82 ± 2.72 months. VitD therapy caused more prominent improvements in BMD and decreases in serum triglycerides as well as mutigated the increase in blood glucose.]]></description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2010.04.054</identifier><identifier>PMID: 20832535</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Azathioprine - therapeutic use ; Biological and medical sciences ; Bone Density - drug effects ; Bone Diseases - epidemiology ; Bone Diseases, Metabolic - epidemiology ; Creatinine - blood ; Diseases of the osteoarticular system ; Female ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Kidney Transplantation - adverse effects ; Kidney Transplantation - immunology ; Kidney Transplantation - physiology ; Lipids - blood ; Male ; Medical sciences ; Methylprednisolone - therapeutic use ; Mycophenolic Acid - analogs & derivatives ; Mycophenolic Acid - therapeutic use ; Osteonecrosis - epidemiology ; Osteoporosis - epidemiology ; Osteoporosis. Osteomalacia. Paget disease ; Sirolimus - therapeutic use ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the urinary system ; Tissue, organ and graft immunology ; Vitamin D - therapeutic use</subject><ispartof>Transplantation proceedings, 2010-09, Vol.42 (7), p.2518-2526</ispartof><rights>Elsevier Inc.</rights><rights>2010 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>2010 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-2fc394c9f2bec1e1ab3a227dcf26a1a74153d0e072c04d08e85057e196671db93</citedby><cites>FETCH-LOGICAL-c464t-2fc394c9f2bec1e1ab3a227dcf26a1a74153d0e072c04d08e85057e196671db93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041134510009346$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23243408$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20832535$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sikgenc, M.M</creatorcontrib><creatorcontrib>Paydas, S</creatorcontrib><creatorcontrib>Balal, M</creatorcontrib><creatorcontrib>Demir, E</creatorcontrib><creatorcontrib>Kurt, C</creatorcontrib><creatorcontrib>Sertdemir, Y</creatorcontrib><creatorcontrib>Binokay, F</creatorcontrib><creatorcontrib>Erken, U</creatorcontrib><title>Bone Disease in Renal Transplantation and Pleotropic Effects of Vitamin D Therapy</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description><![CDATA[Abstract Osteoporosis, osteopenia, and osteonecrosis are common in renal transplant recipients. In this study, we evaluated relationship between bone mineral density (BMD) and posttransplant duration; creatinine clearance; serum levels of glucose, calcium, phosphorus, alkaline phosphatase, vitamin D (vitD), parathormone, magnesium, C telopeptide, osteocalcin, lipids, and vit D therapy. Eighty five subjects included in this study had a mean age of 36.25 ± 10.5 years. At least at 6-month intervals we measured femoral neck (FN) and lumbar vertebra (LV) by DEXA and biochemical parameters. VitD was prescribed in 57 patients (vitDG). The mean duration of posttransplantation follow-up was 9.82 ± 2.72 months. T scores (TS) of FN and LV were normal in 29.4% and 21.2%; osteopenia in 56.5% and 49.4%; and osteoporosis in 12.1% and 29.4% of patients, respectively. Upon follow-up, TS improved significantly from −1.58 to −1.46 in FN and from −1.88 to −1.70 in LV ( P < .05 for both). In patients receiving vitDG, TS improved significantly from −1.74 to −1.61 on FN and from −2.16 to −1.97 on LV ( P < .05 for both). Osteocalcin and vitDG levels decreased in all patients ( P < .05 for all). Blood urea nitrogen and serum creatinine increased ( P < .05). In VitDG cohort, triglyceride levels decreased ( P < .05) with unchanged blood glucose values; but among the other patients, triglycerides were unchanged but glucose levels had increased ( P < .05). Bone disease including osteopenia or osteoporosis was observed among 70%. During the follow-up period, BMD increased significantly from baseline at 9.82 ± 2.72 months. VitD therapy caused more prominent improvements in BMD and decreases in serum triglycerides as well as mutigated the increase in blood glucose.]]></description><subject>Azathioprine - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bone Density - drug effects</subject><subject>Bone Diseases - epidemiology</subject><subject>Bone Diseases, Metabolic - epidemiology</subject><subject>Creatinine - blood</subject><subject>Diseases of the osteoarticular system</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Kidney Transplantation - immunology</subject><subject>Kidney Transplantation - physiology</subject><subject>Lipids - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Methylprednisolone - therapeutic use</subject><subject>Mycophenolic Acid - analogs & derivatives</subject><subject>Mycophenolic Acid - therapeutic use</subject><subject>Osteonecrosis - epidemiology</subject><subject>Osteoporosis - epidemiology</subject><subject>Osteoporosis. Osteomalacia. Paget disease</subject><subject>Sirolimus - therapeutic use</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the urinary system</subject><subject>Tissue, organ and graft immunology</subject><subject>Vitamin D - therapeutic use</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNklurEzEQgIMonlr9CxIE8Wnr5LK7XR-E4-nxAge8VV9Dmp1g6japma3Qf2_W9qD45FMI882Fb4axJwIWAkTzfLsYs420z8kh9gsJJQB6AbW-w2Zi2apKNlLdZTMALSqhdH3BHhBtofylVvfZhYSlkrWqZ-zjqxSRrwKhJeQh8k8Y7cDXvxsMNo52DClyG3v-YcA05rQPjl97j24knjz_Gka7K3krvv6G2e6PD9k9bwfCR-d3zr68vl5fva1u3r95d3V5Uznd6LGS3qlOu87LDTqBwm6UlbLtnZeNFbbVolY9ILTSge5hicsa6hZF1zSt6DedmrNnp7rFw48D0mh2gRwOZWhMBzJtrQFqkBP54kS6nIgyerPPYWfz0Qgwk1GzNX8bNZNRA9oUoyX58bnNYbMrsdvUW4UFeHoGLDk7-FLIBfrDqaJcF3jOVicOi5SfAbMhFzA67EMuMk2fwv_N8_KfMm4IMZTO3_GItE2HXBZIRhiSBszn6QamExBl-53SjfoF0KevVA</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Sikgenc, M.M</creator><creator>Paydas, S</creator><creator>Balal, M</creator><creator>Demir, E</creator><creator>Kurt, C</creator><creator>Sertdemir, Y</creator><creator>Binokay, F</creator><creator>Erken, U</creator><general>Elsevier Inc</general><general>Elsevier</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></search><sort><creationdate>20100901</creationdate><title>Bone Disease in Renal Transplantation and Pleotropic Effects of Vitamin D Therapy</title><author>Sikgenc, M.M ; Paydas, S ; Balal, M ; Demir, E ; Kurt, C ; Sertdemir, Y ; Binokay, F ; Erken, U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-2fc394c9f2bec1e1ab3a227dcf26a1a74153d0e072c04d08e85057e196671db93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Azathioprine - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bone Density - drug effects</topic><topic>Bone Diseases - epidemiology</topic><topic>Bone Diseases, Metabolic - epidemiology</topic><topic>Creatinine - blood</topic><topic>Diseases of the osteoarticular system</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Kidney Transplantation - immunology</topic><topic>Kidney Transplantation - physiology</topic><topic>Lipids - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Methylprednisolone - therapeutic use</topic><topic>Mycophenolic Acid - analogs & derivatives</topic><topic>Mycophenolic Acid - therapeutic use</topic><topic>Osteonecrosis - epidemiology</topic><topic>Osteoporosis - epidemiology</topic><topic>Osteoporosis. Osteomalacia. Paget disease</topic><topic>Sirolimus - therapeutic use</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the urinary system</topic><topic>Tissue, organ and graft immunology</topic><topic>Vitamin D - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sikgenc, M.M</creatorcontrib><creatorcontrib>Paydas, S</creatorcontrib><creatorcontrib>Balal, M</creatorcontrib><creatorcontrib>Demir, E</creatorcontrib><creatorcontrib>Kurt, C</creatorcontrib><creatorcontrib>Sertdemir, Y</creatorcontrib><creatorcontrib>Binokay, F</creatorcontrib><creatorcontrib>Erken, U</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><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sikgenc, M.M</au><au>Paydas, S</au><au>Balal, M</au><au>Demir, E</au><au>Kurt, C</au><au>Sertdemir, Y</au><au>Binokay, F</au><au>Erken, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone Disease in Renal Transplantation and Pleotropic Effects of Vitamin D Therapy</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>42</volume><issue>7</issue><spage>2518</spage><epage>2526</epage><pages>2518-2526</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract><![CDATA[Abstract Osteoporosis, osteopenia, and osteonecrosis are common in renal transplant recipients. In this study, we evaluated relationship between bone mineral density (BMD) and posttransplant duration; creatinine clearance; serum levels of glucose, calcium, phosphorus, alkaline phosphatase, vitamin D (vitD), parathormone, magnesium, C telopeptide, osteocalcin, lipids, and vit D therapy. Eighty five subjects included in this study had a mean age of 36.25 ± 10.5 years. At least at 6-month intervals we measured femoral neck (FN) and lumbar vertebra (LV) by DEXA and biochemical parameters. VitD was prescribed in 57 patients (vitDG). The mean duration of posttransplantation follow-up was 9.82 ± 2.72 months. T scores (TS) of FN and LV were normal in 29.4% and 21.2%; osteopenia in 56.5% and 49.4%; and osteoporosis in 12.1% and 29.4% of patients, respectively. Upon follow-up, TS improved significantly from −1.58 to −1.46 in FN and from −1.88 to −1.70 in LV ( P < .05 for both). In patients receiving vitDG, TS improved significantly from −1.74 to −1.61 on FN and from −2.16 to −1.97 on LV ( P < .05 for both). Osteocalcin and vitDG levels decreased in all patients ( P < .05 for all). Blood urea nitrogen and serum creatinine increased ( P < .05). In VitDG cohort, triglyceride levels decreased ( P < .05) with unchanged blood glucose values; but among the other patients, triglycerides were unchanged but glucose levels had increased ( P < .05). Bone disease including osteopenia or osteoporosis was observed among 70%. During the follow-up period, BMD increased significantly from baseline at 9.82 ± 2.72 months. VitD therapy caused more prominent improvements in BMD and decreases in serum triglycerides as well as mutigated the increase in blood glucose.]]></abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>20832535</pmid><doi>10.1016/j.transproceed.2010.04.054</doi><tpages>9</tpages></addata></record> |
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subjects | Azathioprine - therapeutic use Biological and medical sciences Bone Density - drug effects Bone Diseases - epidemiology Bone Diseases, Metabolic - epidemiology Creatinine - blood Diseases of the osteoarticular system Female Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Kidney Transplantation - adverse effects Kidney Transplantation - immunology Kidney Transplantation - physiology Lipids - blood Male Medical sciences Methylprednisolone - therapeutic use Mycophenolic Acid - analogs & derivatives Mycophenolic Acid - therapeutic use Osteonecrosis - epidemiology Osteoporosis - epidemiology Osteoporosis. Osteomalacia. Paget disease Sirolimus - therapeutic use Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the urinary system Tissue, organ and graft immunology Vitamin D - therapeutic use |
title | Bone Disease in Renal Transplantation and Pleotropic Effects of Vitamin D Therapy |
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