Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation
Aims Abnormal bone metabolism and progressive demineralization have been described in patients with heart failure (HF). We hypothesized that mechanical unloading through implantation of a ventricular assist device (VAD) with subsequent haemodynamic improvement would correct abnormal bone metabolism...
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Veröffentlicht in: | European journal of heart failure 2012-12, Vol.14 (12), p.1356-1365 |
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creator | Wu, Christina Kato, Tomoko S. Pronschinske, Katherine Qiu, Sylvia Naka, Yoshifumi Takayama, Hiroo Schulze-Späte, Ulrike Cremers, Serge Shane, Elizabeth Mancini, Donna Schulze, P. Christian |
description | Aims
Abnormal bone metabolism and progressive demineralization have been described in patients with heart failure (HF). We hypothesized that mechanical unloading through implantation of a ventricular assist device (VAD) with subsequent haemodynamic improvement would correct abnormal bone metabolism in patients with advanced HF.
Methods and results
Serum was collected from 14 controls, 20 patients with moderate HF, 34 patients with advanced HF undergoing VAD implantation, and 34 patients at the time of VAD explantation (mean duration: 169 ± 125 days). Bone metabolism markers were measured using enzyme‐linked immunosorption assay (ELISA) or chemiluminescence immunoassay (CLIA). Compared with controls, HF patients showed increased parathyroid hormone (PTH: 42 ± 19 vs. 117 ± 117 pg/mL in HF; P < 0.02) with decreased 25‐hydroxyvitamin D [25(OH)D: 29 ± 14 vs. 21 ± 11 ng/mL in HF; P = 0.05]. While procollagen‐1 N‐terminal peptide (P1NP) and osteocalcin were similar, cross‐linked C‐ and N‐telopeptides of type I collagen (CTX and NTX) were both higher in HF (NTX: 14 ± 6 vs. 20 ± 11 ng/mL; P < 0.05; CTX: 0.35 ± 0.13 vs. 1.05 ± 0.78 ng/mL; P < 0.01 for controls and HF, respectively). P1NP increased markedly after VAD implantation (49 ± 37 vs. 121 ± 62 ng/mL; P < 0.0001), with a mild decrease in CTX and NTX levels indicating a shift towards anabolic bone formation. Serum PTH correlated with estimated glomerular filtration rate (r = –0.245, P < 0.05).
Conclusion
Patients with advanced HF are characterized by increased levels of biochemical markers of bone resorption potentially as a result of secondary hyperparathyroidism and uncoupling of bone remodelling. Haemodynamic improvement and mechanical unloading after VAD implantation lead to correction of bone metabolism and increased levels of anabolic bone formation markers. |
doi_str_mv | 10.1093/eurjhf/hfs138 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3598377</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1220792621</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4718-7fd38ae87b78cc193afcf94092bb6c190c4e57425ccb7c015576589d7a0613293</originalsourceid><addsrcrecordid>eNp9kUtv1DAUhSMEoqWwZIu8ZBPqRxLbGyRUOh1QKY-CurQc52biktiDncwwf4Tfi0cZRrBhZV_53O-e65Nlzwl-RbBk5zCF-64979pImHiQnRLBZY5FUTxMdyZELkVBT7InMd5jTDjG9HF2QqkUUlT8NPv1duf0YE1EvkW1d4DGKTi_gYAGHb5DiMg6tNajBTdGtLVjhzrQYUSttv0UAGnXoNb3vd9at0KdhsE3MxPZYR0SakitaOyCn1Yd2qQiWDP1OiAdo40jamBjDezVvXZjGuXd0-xRq_sIzw7nWfZtcfn1Yplff7x6d_HmOjcFJyLnbcOEBsFrLowhkunWtLLAktZ1lWpsCih5QUtjam4wKUtelUI2XOOKMCrZWfZ65q6neoDG7M3pXq2DTdvvlNdW_fvibKdWfqNYKQXjPAFeHgDB_5ggjmqw0UCfNgE_RUUoxVzSipIkzWepCT7GAO1xDMFqn6Was1Rzlkn_4m9vR_Wf8JKgnAVb28Pu_zR1-X65WC5uZ_DBSPp8-HnsS3GrROWluru5Ul9u7j5_Yrcf1IL9BvtVw8U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1220792621</pqid></control><display><type>article</type><title>Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library (Open Access Collection)</source><source>Alma/SFX Local Collection</source><creator>Wu, Christina ; Kato, Tomoko S. ; Pronschinske, Katherine ; Qiu, Sylvia ; Naka, Yoshifumi ; Takayama, Hiroo ; Schulze-Späte, Ulrike ; Cremers, Serge ; Shane, Elizabeth ; Mancini, Donna ; Schulze, P. Christian</creator><creatorcontrib>Wu, Christina ; Kato, Tomoko S. ; Pronschinske, Katherine ; Qiu, Sylvia ; Naka, Yoshifumi ; Takayama, Hiroo ; Schulze-Späte, Ulrike ; Cremers, Serge ; Shane, Elizabeth ; Mancini, Donna ; Schulze, P. Christian</creatorcontrib><description>Aims
Abnormal bone metabolism and progressive demineralization have been described in patients with heart failure (HF). We hypothesized that mechanical unloading through implantation of a ventricular assist device (VAD) with subsequent haemodynamic improvement would correct abnormal bone metabolism in patients with advanced HF.
Methods and results
Serum was collected from 14 controls, 20 patients with moderate HF, 34 patients with advanced HF undergoing VAD implantation, and 34 patients at the time of VAD explantation (mean duration: 169 ± 125 days). Bone metabolism markers were measured using enzyme‐linked immunosorption assay (ELISA) or chemiluminescence immunoassay (CLIA). Compared with controls, HF patients showed increased parathyroid hormone (PTH: 42 ± 19 vs. 117 ± 117 pg/mL in HF; P < 0.02) with decreased 25‐hydroxyvitamin D [25(OH)D: 29 ± 14 vs. 21 ± 11 ng/mL in HF; P = 0.05]. While procollagen‐1 N‐terminal peptide (P1NP) and osteocalcin were similar, cross‐linked C‐ and N‐telopeptides of type I collagen (CTX and NTX) were both higher in HF (NTX: 14 ± 6 vs. 20 ± 11 ng/mL; P < 0.05; CTX: 0.35 ± 0.13 vs. 1.05 ± 0.78 ng/mL; P < 0.01 for controls and HF, respectively). P1NP increased markedly after VAD implantation (49 ± 37 vs. 121 ± 62 ng/mL; P < 0.0001), with a mild decrease in CTX and NTX levels indicating a shift towards anabolic bone formation. Serum PTH correlated with estimated glomerular filtration rate (r = –0.245, P < 0.05).
Conclusion
Patients with advanced HF are characterized by increased levels of biochemical markers of bone resorption potentially as a result of secondary hyperparathyroidism and uncoupling of bone remodelling. Haemodynamic improvement and mechanical unloading after VAD implantation lead to correction of bone metabolism and increased levels of anabolic bone formation markers.</description><identifier>ISSN: 1388-9842</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1093/eurjhf/hfs138</identifier><identifier>PMID: 22989867</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Analysis of Variance ; Biomarkers - blood ; Bone metabolism ; Bone Remodeling - physiology ; Bone Resorption - physiopathology ; Case-Control Studies ; Collagen Type I - blood ; Device ; Device Therapy ; Echocardiography ; Enzyme-Linked Immunosorbent Assay ; Female ; Heart failure ; Heart Failure - blood ; Heart Failure - physiopathology ; Heart Failure - therapy ; Heart-Assist Devices ; Hemodynamics - physiology ; Humans ; Luminescence ; Male ; Osteocalcin - blood ; Parathyroid Hormone - blood ; Peptides - blood ; Retrospective Studies ; Statistics, Nonparametric ; Ventricular assist ; Vitamin D - analogs & derivatives ; Vitamin D - blood</subject><ispartof>European journal of heart failure, 2012-12, Vol.14 (12), p.1356-1365</ispartof><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © 2012 the Authors</rights><rights>Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2012. For permissions please email: journals.permissions@oup.com. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4718-7fd38ae87b78cc193afcf94092bb6c190c4e57425ccb7c015576589d7a0613293</citedby><cites>FETCH-LOGICAL-c4718-7fd38ae87b78cc193afcf94092bb6c190c4e57425ccb7c015576589d7a0613293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1093%2Feurjhf%2Fhfs138$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1093%2Feurjhf%2Fhfs138$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22989867$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Christina</creatorcontrib><creatorcontrib>Kato, Tomoko S.</creatorcontrib><creatorcontrib>Pronschinske, Katherine</creatorcontrib><creatorcontrib>Qiu, Sylvia</creatorcontrib><creatorcontrib>Naka, Yoshifumi</creatorcontrib><creatorcontrib>Takayama, Hiroo</creatorcontrib><creatorcontrib>Schulze-Späte, Ulrike</creatorcontrib><creatorcontrib>Cremers, Serge</creatorcontrib><creatorcontrib>Shane, Elizabeth</creatorcontrib><creatorcontrib>Mancini, Donna</creatorcontrib><creatorcontrib>Schulze, P. Christian</creatorcontrib><title>Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation</title><title>European journal of heart failure</title><addtitle>European Journal of Heart Failure</addtitle><description>Aims
Abnormal bone metabolism and progressive demineralization have been described in patients with heart failure (HF). We hypothesized that mechanical unloading through implantation of a ventricular assist device (VAD) with subsequent haemodynamic improvement would correct abnormal bone metabolism in patients with advanced HF.
Methods and results
Serum was collected from 14 controls, 20 patients with moderate HF, 34 patients with advanced HF undergoing VAD implantation, and 34 patients at the time of VAD explantation (mean duration: 169 ± 125 days). Bone metabolism markers were measured using enzyme‐linked immunosorption assay (ELISA) or chemiluminescence immunoassay (CLIA). Compared with controls, HF patients showed increased parathyroid hormone (PTH: 42 ± 19 vs. 117 ± 117 pg/mL in HF; P < 0.02) with decreased 25‐hydroxyvitamin D [25(OH)D: 29 ± 14 vs. 21 ± 11 ng/mL in HF; P = 0.05]. While procollagen‐1 N‐terminal peptide (P1NP) and osteocalcin were similar, cross‐linked C‐ and N‐telopeptides of type I collagen (CTX and NTX) were both higher in HF (NTX: 14 ± 6 vs. 20 ± 11 ng/mL; P < 0.05; CTX: 0.35 ± 0.13 vs. 1.05 ± 0.78 ng/mL; P < 0.01 for controls and HF, respectively). P1NP increased markedly after VAD implantation (49 ± 37 vs. 121 ± 62 ng/mL; P < 0.0001), with a mild decrease in CTX and NTX levels indicating a shift towards anabolic bone formation. Serum PTH correlated with estimated glomerular filtration rate (r = –0.245, P < 0.05).
Conclusion
Patients with advanced HF are characterized by increased levels of biochemical markers of bone resorption potentially as a result of secondary hyperparathyroidism and uncoupling of bone remodelling. Haemodynamic improvement and mechanical unloading after VAD implantation lead to correction of bone metabolism and increased levels of anabolic bone formation markers.</description><subject>Analysis of Variance</subject><subject>Biomarkers - blood</subject><subject>Bone metabolism</subject><subject>Bone Remodeling - physiology</subject><subject>Bone Resorption - physiopathology</subject><subject>Case-Control Studies</subject><subject>Collagen Type I - blood</subject><subject>Device</subject><subject>Device Therapy</subject><subject>Echocardiography</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Heart failure</subject><subject>Heart Failure - blood</subject><subject>Heart Failure - physiopathology</subject><subject>Heart Failure - therapy</subject><subject>Heart-Assist Devices</subject><subject>Hemodynamics - physiology</subject><subject>Humans</subject><subject>Luminescence</subject><subject>Male</subject><subject>Osteocalcin - blood</subject><subject>Parathyroid Hormone - blood</subject><subject>Peptides - blood</subject><subject>Retrospective Studies</subject><subject>Statistics, Nonparametric</subject><subject>Ventricular assist</subject><subject>Vitamin D - analogs & derivatives</subject><subject>Vitamin D - blood</subject><issn>1388-9842</issn><issn>1879-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUtv1DAUhSMEoqWwZIu8ZBPqRxLbGyRUOh1QKY-CurQc52biktiDncwwf4Tfi0cZRrBhZV_53O-e65Nlzwl-RbBk5zCF-64979pImHiQnRLBZY5FUTxMdyZELkVBT7InMd5jTDjG9HF2QqkUUlT8NPv1duf0YE1EvkW1d4DGKTi_gYAGHb5DiMg6tNajBTdGtLVjhzrQYUSttv0UAGnXoNb3vd9at0KdhsE3MxPZYR0SakitaOyCn1Yd2qQiWDP1OiAdo40jamBjDezVvXZjGuXd0-xRq_sIzw7nWfZtcfn1Yplff7x6d_HmOjcFJyLnbcOEBsFrLowhkunWtLLAktZ1lWpsCih5QUtjam4wKUtelUI2XOOKMCrZWfZ65q6neoDG7M3pXq2DTdvvlNdW_fvibKdWfqNYKQXjPAFeHgDB_5ggjmqw0UCfNgE_RUUoxVzSipIkzWepCT7GAO1xDMFqn6Was1Rzlkn_4m9vR_Wf8JKgnAVb28Pu_zR1-X65WC5uZ_DBSPp8-HnsS3GrROWluru5Ul9u7j5_Yrcf1IL9BvtVw8U</recordid><startdate>201212</startdate><enddate>201212</enddate><creator>Wu, Christina</creator><creator>Kato, Tomoko S.</creator><creator>Pronschinske, Katherine</creator><creator>Qiu, Sylvia</creator><creator>Naka, Yoshifumi</creator><creator>Takayama, Hiroo</creator><creator>Schulze-Späte, Ulrike</creator><creator>Cremers, Serge</creator><creator>Shane, Elizabeth</creator><creator>Mancini, Donna</creator><creator>Schulze, P. Christian</creator><general>Blackwell Publishing Ltd</general><general>Oxford University Press</general><scope>BSCLL</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>5PM</scope></search><sort><creationdate>201212</creationdate><title>Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation</title><author>Wu, Christina ; Kato, Tomoko S. ; Pronschinske, Katherine ; Qiu, Sylvia ; Naka, Yoshifumi ; Takayama, Hiroo ; Schulze-Späte, Ulrike ; Cremers, Serge ; Shane, Elizabeth ; Mancini, Donna ; Schulze, P. Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4718-7fd38ae87b78cc193afcf94092bb6c190c4e57425ccb7c015576589d7a0613293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analysis of Variance</topic><topic>Biomarkers - blood</topic><topic>Bone metabolism</topic><topic>Bone Remodeling - physiology</topic><topic>Bone Resorption - physiopathology</topic><topic>Case-Control Studies</topic><topic>Collagen Type I - blood</topic><topic>Device</topic><topic>Device Therapy</topic><topic>Echocardiography</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Heart failure</topic><topic>Heart Failure - blood</topic><topic>Heart Failure - physiopathology</topic><topic>Heart Failure - therapy</topic><topic>Heart-Assist Devices</topic><topic>Hemodynamics - physiology</topic><topic>Humans</topic><topic>Luminescence</topic><topic>Male</topic><topic>Osteocalcin - blood</topic><topic>Parathyroid Hormone - blood</topic><topic>Peptides - blood</topic><topic>Retrospective Studies</topic><topic>Statistics, Nonparametric</topic><topic>Ventricular assist</topic><topic>Vitamin D - analogs & derivatives</topic><topic>Vitamin D - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Christina</creatorcontrib><creatorcontrib>Kato, Tomoko S.</creatorcontrib><creatorcontrib>Pronschinske, Katherine</creatorcontrib><creatorcontrib>Qiu, Sylvia</creatorcontrib><creatorcontrib>Naka, Yoshifumi</creatorcontrib><creatorcontrib>Takayama, Hiroo</creatorcontrib><creatorcontrib>Schulze-Späte, Ulrike</creatorcontrib><creatorcontrib>Cremers, Serge</creatorcontrib><creatorcontrib>Shane, Elizabeth</creatorcontrib><creatorcontrib>Mancini, Donna</creatorcontrib><creatorcontrib>Schulze, P. Christian</creatorcontrib><collection>Istex</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>PubMed Central (Full Participant titles)</collection><jtitle>European journal of heart failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Christina</au><au>Kato, Tomoko S.</au><au>Pronschinske, Katherine</au><au>Qiu, Sylvia</au><au>Naka, Yoshifumi</au><au>Takayama, Hiroo</au><au>Schulze-Späte, Ulrike</au><au>Cremers, Serge</au><au>Shane, Elizabeth</au><au>Mancini, Donna</au><au>Schulze, P. Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation</atitle><jtitle>European journal of heart failure</jtitle><addtitle>European Journal of Heart Failure</addtitle><date>2012-12</date><risdate>2012</risdate><volume>14</volume><issue>12</issue><spage>1356</spage><epage>1365</epage><pages>1356-1365</pages><issn>1388-9842</issn><eissn>1879-0844</eissn><abstract>Aims
Abnormal bone metabolism and progressive demineralization have been described in patients with heart failure (HF). We hypothesized that mechanical unloading through implantation of a ventricular assist device (VAD) with subsequent haemodynamic improvement would correct abnormal bone metabolism in patients with advanced HF.
Methods and results
Serum was collected from 14 controls, 20 patients with moderate HF, 34 patients with advanced HF undergoing VAD implantation, and 34 patients at the time of VAD explantation (mean duration: 169 ± 125 days). Bone metabolism markers were measured using enzyme‐linked immunosorption assay (ELISA) or chemiluminescence immunoassay (CLIA). Compared with controls, HF patients showed increased parathyroid hormone (PTH: 42 ± 19 vs. 117 ± 117 pg/mL in HF; P < 0.02) with decreased 25‐hydroxyvitamin D [25(OH)D: 29 ± 14 vs. 21 ± 11 ng/mL in HF; P = 0.05]. While procollagen‐1 N‐terminal peptide (P1NP) and osteocalcin were similar, cross‐linked C‐ and N‐telopeptides of type I collagen (CTX and NTX) were both higher in HF (NTX: 14 ± 6 vs. 20 ± 11 ng/mL; P < 0.05; CTX: 0.35 ± 0.13 vs. 1.05 ± 0.78 ng/mL; P < 0.01 for controls and HF, respectively). P1NP increased markedly after VAD implantation (49 ± 37 vs. 121 ± 62 ng/mL; P < 0.0001), with a mild decrease in CTX and NTX levels indicating a shift towards anabolic bone formation. Serum PTH correlated with estimated glomerular filtration rate (r = –0.245, P < 0.05).
Conclusion
Patients with advanced HF are characterized by increased levels of biochemical markers of bone resorption potentially as a result of secondary hyperparathyroidism and uncoupling of bone remodelling. Haemodynamic improvement and mechanical unloading after VAD implantation lead to correction of bone metabolism and increased levels of anabolic bone formation markers.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>22989867</pmid><doi>10.1093/eurjhf/hfs138</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via Wiley Online Library; EZB-FREE-00999 freely available EZB journals; Wiley Online Library (Open Access Collection); Alma/SFX Local Collection |
subjects | Analysis of Variance Biomarkers - blood Bone metabolism Bone Remodeling - physiology Bone Resorption - physiopathology Case-Control Studies Collagen Type I - blood Device Device Therapy Echocardiography Enzyme-Linked Immunosorbent Assay Female Heart failure Heart Failure - blood Heart Failure - physiopathology Heart Failure - therapy Heart-Assist Devices Hemodynamics - physiology Humans Luminescence Male Osteocalcin - blood Parathyroid Hormone - blood Peptides - blood Retrospective Studies Statistics, Nonparametric Ventricular assist Vitamin D - analogs & derivatives Vitamin D - blood |
title | Dynamics of bone turnover markers in patients with heart failure and following haemodynamic improvement through ventricular assist device implantation |
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