Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1998-12-22
pubmed:abstractText
Biochemical markers of bone turnover are often measured in patients treated with antiresorptive agents to monitor the effects of therapy. In order for a change in these markers to clearly indicate treatment effect, the change in the markers must exceed the amount of spontaneous variation typically seen with no treatment. Based on the measured long-term variability of markers in untreated patients, we defined a minimum significant change (MSC), that is, a change that was sufficiently large that it was unlikely to be due to spontaneous variability. We also examined the changes in markers of bone turnover in subjects treated with pamidronate to see how often observed changes in turnover after treatment exceeded the MSC. We found that urinary markers of bone resorption are best measured on 2-hour fasting samples, because results on random urine showed poor precision and less decline with therapy. We also found that of all the markers, urinary N-telopeptide cross-links (NTX) had the greatest decline after therapy (58%), although it also had the highest long-term variability (29.5%). The marker that most often showed a decline with treatment that exceeded the MSC was serum bone-specific alkaline phosphatase where 74% of observed changes exceeded the MSC. Other markers that often showed a decline with treatment that exceeded the MSC were 2-hour fasting urine NTX and free deoxypyridinoline, where 57% and 48%, respectively, of changes in therapy exceeded the MSC. The ideal marker would combine the large decline after treatment characteristic of NTX (60-70%) with the good precision of bone-specific alkaline phosphatase.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Alkaline Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Amino Acids, http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Biological Markers, http://linkedlifedata.com/resource/pubmed/chemical/Collagen, http://linkedlifedata.com/resource/pubmed/chemical/Collagen Type I, http://linkedlifedata.com/resource/pubmed/chemical/Creatinine, http://linkedlifedata.com/resource/pubmed/chemical/Diphosphonates, http://linkedlifedata.com/resource/pubmed/chemical/Osteocalcin, http://linkedlifedata.com/resource/pubmed/chemical/Peptides, http://linkedlifedata.com/resource/pubmed/chemical/Thyroxine, http://linkedlifedata.com/resource/pubmed/chemical/collagen type I trimeric..., http://linkedlifedata.com/resource/pubmed/chemical/deoxypyridinoline, http://linkedlifedata.com/resource/pubmed/chemical/pamidronate, http://linkedlifedata.com/resource/pubmed/chemical/pyridinoline
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0171-967X
pubmed:author
pubmed:issnType
Print
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
363-8
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:9799818-Alkaline Phosphatase, pubmed-meshheading:9799818-Amino Acids, pubmed-meshheading:9799818-Antineoplastic Agents, pubmed-meshheading:9799818-Biological Markers, pubmed-meshheading:9799818-Bone Resorption, pubmed-meshheading:9799818-Bone and Bones, pubmed-meshheading:9799818-Carcinoma, Papillary, pubmed-meshheading:9799818-Collagen, pubmed-meshheading:9799818-Collagen Type I, pubmed-meshheading:9799818-Creatinine, pubmed-meshheading:9799818-Diphosphonates, pubmed-meshheading:9799818-Double-Blind Method, pubmed-meshheading:9799818-Fasting, pubmed-meshheading:9799818-Humans, pubmed-meshheading:9799818-Osteocalcin, pubmed-meshheading:9799818-Osteolysis, pubmed-meshheading:9799818-Peptides, pubmed-meshheading:9799818-Thyroid Neoplasms, pubmed-meshheading:9799818-Thyroxine
pubmed:year
1998
pubmed:articleTitle
Utility of biochemical markers of bone turnover in the follow-up of patients treated with bisphosphonates.
pubmed:affiliation
The Charles A. Dana Research Institute and the Harvard-Thorndike Laboratory of the Beth Israel Deaconess Medical Center, Department of Medicine, Division of Gerontology, Boston, Massachusetts 02215, USA.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, U.S. Gov't, P.H.S., Randomized Controlled Trial, Research Support, Non-U.S. Gov't