<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Granke M</submitter><funding>BLRD VA</funding><funding>NCATS NIH HHS</funding><funding>NIBIB NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIAMS NIH HHS</funding><pagination>1290-300</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4478129</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30(7)</volume><pubmed_abstract>Fracture risk does not solely depend on strength but also on fracture toughness; ie, the ability of bone material to resist crack initiation and propagation. Because resistance to crack growth largely depends on bone properties at the tissue level, including collagen characteristics, current X-ray based assessment tools may not be suitable to identify age-related, disease-related, or treatment-related changes in fracture toughness. To identify useful clinical surrogates that could improve the assessment of fracture resistance, we investigated the potential of (1)H nuclear magnetic resonance spectroscopy (NMR) and reference point indentation (RPI) to explain age-related variance in fracture toughness. Harvested from cadaveric femurs (62 human donors), single-edge notched beam (SENB) specime</pubmed_abstract><journal>Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research</journal><pubmed_title>Identifying Novel Clinical Surrogates to Assess Human Bone Fracture Toughness.</pubmed_title><pmcid>PMC4478129</pmcid><funding_grant_id>AR063157</funding_grant_id><funding_grant_id>UL1 RR024975</funding_grant_id><funding_grant_id>R01 EB014308</funding_grant_id><funding_grant_id>S10 RR027631</funding_grant_id><funding_grant_id>UL1 TR000445</funding_grant_id><funding_grant_id>1S10RR027631</funding_grant_id><funding_grant_id>R01 AR063157</funding_grant_id><funding_grant_id>I01 BX001018</funding_grant_id><pubmed_authors>Makowski AJ</pubmed_authors><pubmed_authors>Uppuganti S</pubmed_authors><pubmed_authors>Does MD</pubmed_authors><pubmed_authors>Nyman JS</pubmed_authors><pubmed_authors>Granke M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identifying Novel Clinical Surrogates to Assess Human Bone Fracture Toughness.</name><description>Fracture risk does not solely depend on strength but also on fracture toughness; ie, the ability of bone material to resist crack initiation and propagation. Because resistance to crack growth largely depends on bone properties at the tissue level, including collagen characteristics, current X-ray based assessment tools may not be suitable to identify age-related, disease-related, or treatment-related changes in fracture toughness. To identify useful clinical surrogates that could improve the assessment of fracture resistance, we investigated the potential of (1)H nuclear magnetic resonance spectroscopy (NMR) and reference point indentation (RPI) to explain age-related variance in fracture toughness. Harvested from cadaveric femurs (62 human donors), single-edge notched beam (SENB) specime</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jul</publication><modification>2025-04-04T02:23:52.504Z</modification><creation>2019-03-27T01:53:55Z</creation></dates><accession>S-EPMC4478129</accession><cross_references><pubmed>25639628</pubmed><doi>10.1002/jbmr.2452</doi></cross_references></HashMap>