The prevalence and incidence of vertebral fractures in end-stage renal disease and the role of parathyroid hormone

Summary The risk of vertebral fracture is unclear in end-stage renal disease. We report a high vertebral fracture prevalence and incidence in transplantation-eligible patients on dialysis, suggesting that these patients may benefit from radiographic screening for vertebral fractures. Parathyroid hor...

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Veröffentlicht in:Osteoporosis international 2020-03, Vol.31 (3), p.515-524
Hauptverfasser: Jansz, T. T., Goto, N. A., van Ballegooijen, A. J., Willems, H. C., Verhaar, M. C., van Jaarsveld, B. C.
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container_end_page 524
container_issue 3
container_start_page 515
container_title Osteoporosis international
container_volume 31
creator Jansz, T. T.
Goto, N. A.
van Ballegooijen, A. J.
Willems, H. C.
Verhaar, M. C.
van Jaarsveld, B. C.
description Summary The risk of vertebral fracture is unclear in end-stage renal disease. We report a high vertebral fracture prevalence and incidence in transplantation-eligible patients on dialysis, suggesting that these patients may benefit from radiographic screening for vertebral fractures. Parathyroid hormone had a U-shaped association with vertebral fracture risk. Introduction Vertebral fractures are often overlooked, but even undiagnosed vertebral fractures negatively impact physical functioning, quality of life, and mortality. The risk of vertebral fractures in end-stage renal disease (ESRD) patients is unclear, and parathyroid hormone (PTH) might play a role in the development of vertebral fractures. We therefore determined vertebral fracture prevalence and incidence in ESRD patients and assessed associations of vertebral trabecular bone mineral density (BMD) and PTH with vertebral fracture. Methods In 146 transplantation-eligible patients on dialysis, we determined vertebral fractures on lateral chest radiographs, which image the thoracic and upper lumbar spine. We determined incident vertebral fractures in 70 patients with follow-up radiographs (23 received a kidney transplant) after median 1.8 years. Vertebral trabecular BMD was measured with computed tomography, and PTH measured with 2-site immunoassays, categorized in tertiles with the middle tertile as reference. We used Poisson regression to assess associations of vertebral trabecular BMD and PTH with vertebral fracture. Results Mean age of the study population was 52 ± 13 years, and 98 (67%) were male. Median dialysis duration was 26 (IQR 13–55) months. Vertebral fractures were present in 50/146 patients (34%) and incident vertebral fractures occurred in 20/70 patients (29%). Vertebral trabecular BMD was not associated with vertebral fracture prevalence (relative risk 0.97, 95% CI 0.89 to 1.04). For the lowest PTH tertile (< 11 pmol/L), the relative risk of vertebral fracture was greater although not significant (2.28, 95% CI 0.97 to 5.97) and was significantly greater for the highest PTH tertile (≥ 30 pmol/L; 2.82, 95% CI 1.22 to 7.27) after adjustment for potential confounders. Conclusions The prevalence and incidence of vertebral fractures is high even in relatively young and healthy ESRD patients. Vertebral trabecular BMD is not associated with vertebral fracture, and the association of PTH with vertebral fracture risk appears U-shaped. Nevertheless, our study did not measure vertebral BMD using
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T. ; Goto, N. A. ; van Ballegooijen, A. J. ; Willems, H. C. ; Verhaar, M. C. ; van Jaarsveld, B. C.</creator><creatorcontrib>Jansz, T. T. ; Goto, N. A. ; van Ballegooijen, A. J. ; Willems, H. C. ; Verhaar, M. C. ; van Jaarsveld, B. C.</creatorcontrib><description>Summary The risk of vertebral fracture is unclear in end-stage renal disease. We report a high vertebral fracture prevalence and incidence in transplantation-eligible patients on dialysis, suggesting that these patients may benefit from radiographic screening for vertebral fractures. Parathyroid hormone had a U-shaped association with vertebral fracture risk. Introduction Vertebral fractures are often overlooked, but even undiagnosed vertebral fractures negatively impact physical functioning, quality of life, and mortality. The risk of vertebral fractures in end-stage renal disease (ESRD) patients is unclear, and parathyroid hormone (PTH) might play a role in the development of vertebral fractures. We therefore determined vertebral fracture prevalence and incidence in ESRD patients and assessed associations of vertebral trabecular bone mineral density (BMD) and PTH with vertebral fracture. Methods In 146 transplantation-eligible patients on dialysis, we determined vertebral fractures on lateral chest radiographs, which image the thoracic and upper lumbar spine. We determined incident vertebral fractures in 70 patients with follow-up radiographs (23 received a kidney transplant) after median 1.8 years. Vertebral trabecular BMD was measured with computed tomography, and PTH measured with 2-site immunoassays, categorized in tertiles with the middle tertile as reference. We used Poisson regression to assess associations of vertebral trabecular BMD and PTH with vertebral fracture. Results Mean age of the study population was 52 ± 13 years, and 98 (67%) were male. Median dialysis duration was 26 (IQR 13–55) months. Vertebral fractures were present in 50/146 patients (34%) and incident vertebral fractures occurred in 20/70 patients (29%). Vertebral trabecular BMD was not associated with vertebral fracture prevalence (relative risk 0.97, 95% CI 0.89 to 1.04). For the lowest PTH tertile (&lt; 11 pmol/L), the relative risk of vertebral fracture was greater although not significant (2.28, 95% CI 0.97 to 5.97) and was significantly greater for the highest PTH tertile (≥ 30 pmol/L; 2.82, 95% CI 1.22 to 7.27) after adjustment for potential confounders. Conclusions The prevalence and incidence of vertebral fractures is high even in relatively young and healthy ESRD patients. Vertebral trabecular BMD is not associated with vertebral fracture, and the association of PTH with vertebral fracture risk appears U-shaped. Nevertheless, our study did not measure vertebral BMD using DXA and assessed vertebral fractures using lateral chest radiographs and not spine radiographs.</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-019-05187-0</identifier><identifier>PMID: 31728605</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Adult ; Aged ; Bone Density ; Bone mineral density ; Cancellous bone ; Chest ; Computed tomography ; Dialysis ; Dual energy X-ray absorptiometry ; End-stage renal disease ; Endocrinology ; Fractures ; Health risk assessment ; Hemodialysis ; Humans ; Incidence ; Kidney diseases ; Kidney Failure, Chronic - complications ; Kidney Failure, Chronic - epidemiology ; Kidney transplantation ; Male ; Medicine ; Medicine &amp; Public Health ; Middle Aged ; Original ; Original Article ; Orthopedics ; Osteoporosis ; Parathyroid ; Parathyroid Hormone ; Population studies ; Prevalence ; Quality of Life ; Radiography ; Rheumatology ; Spinal Fractures - diagnostic imaging ; Spinal Fractures - epidemiology ; Spinal Fractures - etiology ; Spine (lumbar) ; Transplants &amp; implants ; Vertebrae</subject><ispartof>Osteoporosis international, 2020-03, Vol.31 (3), p.515-524</ispartof><rights>The Author(s) 2019</rights><rights>Osteoporosis International is a copyright of Springer, (2019). All Rights Reserved. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-5366cbd708a5200b351d85a45b37b1e599228684f887eb77f51c3347a535a5473</citedby><cites>FETCH-LOGICAL-c474t-5366cbd708a5200b351d85a45b37b1e599228684f887eb77f51c3347a535a5473</cites><orcidid>0000-0002-5686-5033</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00198-019-05187-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00198-019-05187-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31728605$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jansz, T. T.</creatorcontrib><creatorcontrib>Goto, N. A.</creatorcontrib><creatorcontrib>van Ballegooijen, A. J.</creatorcontrib><creatorcontrib>Willems, H. C.</creatorcontrib><creatorcontrib>Verhaar, M. C.</creatorcontrib><creatorcontrib>van Jaarsveld, B. C.</creatorcontrib><title>The prevalence and incidence of vertebral fractures in end-stage renal disease and the role of parathyroid hormone</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><description>Summary The risk of vertebral fracture is unclear in end-stage renal disease. We report a high vertebral fracture prevalence and incidence in transplantation-eligible patients on dialysis, suggesting that these patients may benefit from radiographic screening for vertebral fractures. Parathyroid hormone had a U-shaped association with vertebral fracture risk. Introduction Vertebral fractures are often overlooked, but even undiagnosed vertebral fractures negatively impact physical functioning, quality of life, and mortality. The risk of vertebral fractures in end-stage renal disease (ESRD) patients is unclear, and parathyroid hormone (PTH) might play a role in the development of vertebral fractures. We therefore determined vertebral fracture prevalence and incidence in ESRD patients and assessed associations of vertebral trabecular bone mineral density (BMD) and PTH with vertebral fracture. Methods In 146 transplantation-eligible patients on dialysis, we determined vertebral fractures on lateral chest radiographs, which image the thoracic and upper lumbar spine. We determined incident vertebral fractures in 70 patients with follow-up radiographs (23 received a kidney transplant) after median 1.8 years. Vertebral trabecular BMD was measured with computed tomography, and PTH measured with 2-site immunoassays, categorized in tertiles with the middle tertile as reference. We used Poisson regression to assess associations of vertebral trabecular BMD and PTH with vertebral fracture. Results Mean age of the study population was 52 ± 13 years, and 98 (67%) were male. Median dialysis duration was 26 (IQR 13–55) months. Vertebral fractures were present in 50/146 patients (34%) and incident vertebral fractures occurred in 20/70 patients (29%). Vertebral trabecular BMD was not associated with vertebral fracture prevalence (relative risk 0.97, 95% CI 0.89 to 1.04). For the lowest PTH tertile (&lt; 11 pmol/L), the relative risk of vertebral fracture was greater although not significant (2.28, 95% CI 0.97 to 5.97) and was significantly greater for the highest PTH tertile (≥ 30 pmol/L; 2.82, 95% CI 1.22 to 7.27) after adjustment for potential confounders. Conclusions The prevalence and incidence of vertebral fractures is high even in relatively young and healthy ESRD patients. Vertebral trabecular BMD is not associated with vertebral fracture, and the association of PTH with vertebral fracture risk appears U-shaped. Nevertheless, our study did not measure vertebral BMD using DXA and assessed vertebral fractures using lateral chest radiographs and not spine radiographs.</description><subject>Adult</subject><subject>Aged</subject><subject>Bone Density</subject><subject>Bone mineral density</subject><subject>Cancellous bone</subject><subject>Chest</subject><subject>Computed tomography</subject><subject>Dialysis</subject><subject>Dual energy X-ray absorptiometry</subject><subject>End-stage renal disease</subject><subject>Endocrinology</subject><subject>Fractures</subject><subject>Health risk assessment</subject><subject>Hemodialysis</subject><subject>Humans</subject><subject>Incidence</subject><subject>Kidney diseases</subject><subject>Kidney Failure, Chronic - complications</subject><subject>Kidney Failure, Chronic - epidemiology</subject><subject>Kidney transplantation</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Osteoporosis</subject><subject>Parathyroid</subject><subject>Parathyroid Hormone</subject><subject>Population studies</subject><subject>Prevalence</subject><subject>Quality of Life</subject><subject>Radiography</subject><subject>Rheumatology</subject><subject>Spinal Fractures - diagnostic imaging</subject><subject>Spinal Fractures - epidemiology</subject><subject>Spinal Fractures - etiology</subject><subject>Spine (lumbar)</subject><subject>Transplants &amp; implants</subject><subject>Vertebrae</subject><issn>0937-941X</issn><issn>1433-2965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUFP3DAQha2Kqmyhf4ADisSFi4sd27FzqVQhKJWQuFCJm-U4k92grL0dJyvx7_FuKNAeehnLmu-98fgRcsLZV86YvkiM8drQXChT3GjKPpAFl0LQsq7UAVmwWmhaS_5wSD6n9MiyqK71J3IouC5NxdSC4P0Kig3C1g0QPBQutEUffN_ub7ErtoAjNOiGokPnxwkhZaCA0NI0uiUUCCE32z6BS7N-zJYYh71849CNqyeMfVusIq5jgGPysXNDgi8v5xH5dX11f3lDb-9-_Lz8fku91HKkSlSVb1rNjFMlY41QvDXKSdUI3XBQdV3mHYzsjNHQaN0p7oWQ2imhnJJaHJFvs-9matbQeghjXsNusF87fLLR9fbvTuhXdhm3VjNdsYpng_MXA4y_J0ijXffJwzC4AHFKthRc7YIwLKNn_6CPccL8MTtK64pLLlSmypnyGFNC6F4fw5ndOdk5UpuL3Udqd9an79d4lfzJMANiBlJuhSXg2-z_2D4D5dis7A</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Jansz, T. 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T.</au><au>Goto, N. A.</au><au>van Ballegooijen, A. J.</au><au>Willems, H. C.</au><au>Verhaar, M. C.</au><au>van Jaarsveld, B. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The prevalence and incidence of vertebral fractures in end-stage renal disease and the role of parathyroid hormone</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2020-03-01</date><risdate>2020</risdate><volume>31</volume><issue>3</issue><spage>515</spage><epage>524</epage><pages>515-524</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>Summary The risk of vertebral fracture is unclear in end-stage renal disease. We report a high vertebral fracture prevalence and incidence in transplantation-eligible patients on dialysis, suggesting that these patients may benefit from radiographic screening for vertebral fractures. Parathyroid hormone had a U-shaped association with vertebral fracture risk. Introduction Vertebral fractures are often overlooked, but even undiagnosed vertebral fractures negatively impact physical functioning, quality of life, and mortality. The risk of vertebral fractures in end-stage renal disease (ESRD) patients is unclear, and parathyroid hormone (PTH) might play a role in the development of vertebral fractures. We therefore determined vertebral fracture prevalence and incidence in ESRD patients and assessed associations of vertebral trabecular bone mineral density (BMD) and PTH with vertebral fracture. Methods In 146 transplantation-eligible patients on dialysis, we determined vertebral fractures on lateral chest radiographs, which image the thoracic and upper lumbar spine. We determined incident vertebral fractures in 70 patients with follow-up radiographs (23 received a kidney transplant) after median 1.8 years. Vertebral trabecular BMD was measured with computed tomography, and PTH measured with 2-site immunoassays, categorized in tertiles with the middle tertile as reference. We used Poisson regression to assess associations of vertebral trabecular BMD and PTH with vertebral fracture. Results Mean age of the study population was 52 ± 13 years, and 98 (67%) were male. Median dialysis duration was 26 (IQR 13–55) months. Vertebral fractures were present in 50/146 patients (34%) and incident vertebral fractures occurred in 20/70 patients (29%). Vertebral trabecular BMD was not associated with vertebral fracture prevalence (relative risk 0.97, 95% CI 0.89 to 1.04). For the lowest PTH tertile (&lt; 11 pmol/L), the relative risk of vertebral fracture was greater although not significant (2.28, 95% CI 0.97 to 5.97) and was significantly greater for the highest PTH tertile (≥ 30 pmol/L; 2.82, 95% CI 1.22 to 7.27) after adjustment for potential confounders. Conclusions The prevalence and incidence of vertebral fractures is high even in relatively young and healthy ESRD patients. Vertebral trabecular BMD is not associated with vertebral fracture, and the association of PTH with vertebral fracture risk appears U-shaped. Nevertheless, our study did not measure vertebral BMD using DXA and assessed vertebral fractures using lateral chest radiographs and not spine radiographs.</abstract><cop>London</cop><pub>Springer London</pub><pmid>31728605</pmid><doi>10.1007/s00198-019-05187-0</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-5686-5033</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; SpringerNature Journals
subjects Adult
Aged
Bone Density
Bone mineral density
Cancellous bone
Chest
Computed tomography
Dialysis
Dual energy X-ray absorptiometry
End-stage renal disease
Endocrinology
Fractures
Health risk assessment
Hemodialysis
Humans
Incidence
Kidney diseases
Kidney Failure, Chronic - complications
Kidney Failure, Chronic - epidemiology
Kidney transplantation
Male
Medicine
Medicine & Public Health
Middle Aged
Original
Original Article
Orthopedics
Osteoporosis
Parathyroid
Parathyroid Hormone
Population studies
Prevalence
Quality of Life
Radiography
Rheumatology
Spinal Fractures - diagnostic imaging
Spinal Fractures - epidemiology
Spinal Fractures - etiology
Spine (lumbar)
Transplants & implants
Vertebrae
title The prevalence and incidence of vertebral fractures in end-stage renal disease and the role of parathyroid hormone
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