<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang Z</submitter><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Institute on Aging</funding><funding>NIMH NIH HHS</funding><funding>NIAMS NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | National Institutes of Health</funding><pagination>39</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6976694</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(1)</volume><pubmed_abstract>Osteoporosis is a highly prevalent chronic aging-related disease that frequently is only detected after fracture. We hypothesized that aminobutyric acids could serve as biomarkers for osteoporosis. We developed a quick, accurate, and sensitive screening method for aminobutyric acid isomers and enantiomers yielding correlations with bone mineral density (BMD) and osteoporotic fracture. In serum, γ-aminobutyric acid (GABA) and (R)-3-aminoisobutyric acid (D-BAIBA) have positive associations with physical activity in young lean women. D-BAIBA positively associated with hip BMD in older individuals without osteoporosis/osteopenia. Lower levels of GABA were observed in 60-80 year old women with osteoporotic fractures. Single nucleotide polymorphisms in seven genes related to these metabolites as</pubmed_abstract><journal>Communications biology</journal><pubmed_title>Quantification of aminobutyric acids and their clinical applications as biomarkers for osteoporosis.</pubmed_title><pmcid>PMC6976694</pmcid><funding_grant_id>P20 GM109036</funding_grant_id><funding_grant_id>R01 AG056504</funding_grant_id><funding_grant_id>R01 AR059781</funding_grant_id><funding_grant_id>R01 DK115679</funding_grant_id><funding_grant_id>P01 AG039355</funding_grant_id><funding_grant_id>R01AG056504</funding_grant_id><funding_grant_id>U19 AG055373</funding_grant_id><funding_grant_id>R01 AR069055</funding_grant_id><funding_grant_id>R01 MH107354</funding_grant_id><funding_grant_id>R01 MH104680</funding_grant_id><funding_grant_id>R01 AG060341</funding_grant_id><funding_grant_id>PO1 AG039355</funding_grant_id><funding_grant_id>R01 GM109068</funding_grant_id><pubmed_authors>Mo C</pubmed_authors><pubmed_authors>Recker R</pubmed_authors><pubmed_authors>Lappe J</pubmed_authors><pubmed_authors>Armstrong DW</pubmed_authors><pubmed_authors>Deng HW</pubmed_authors><pubmed_authors>Brotto M</pubmed_authors><pubmed_authors>Bonewald LF</pubmed_authors><pubmed_authors>Shen H</pubmed_authors><pubmed_authors>Zhao LJ</pubmed_authors><pubmed_authors>Lee JT</pubmed_authors><pubmed_authors>Bian L</pubmed_authors><pubmed_authors>Su KJ</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Kukula M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantification of aminobutyric acids and their clinical applications as biomarkers for osteoporosis.</name><description>Osteoporosis is a highly prevalent chronic aging-related disease that frequently is only detected after fracture. We hypothesized that aminobutyric acids could serve as biomarkers for osteoporosis. We developed a quick, accurate, and sensitive screening method for aminobutyric acid isomers and enantiomers yielding correlations with bone mineral density (BMD) and osteoporotic fracture. In serum, γ-aminobutyric acid (GABA) and (R)-3-aminoisobutyric acid (D-BAIBA) have positive associations with physical activity in young lean women. D-BAIBA positively associated with hip BMD in older individuals without osteoporosis/osteopenia. Lower levels of GABA were observed in 60-80 year old women with osteoporotic fractures. Single nucleotide polymorphisms in seven genes related to these metabolites as</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2026-05-13T16:04:02.622Z</modification><creation>2020-05-22T08:58:57Z</creation></dates><accession>S-EPMC6976694</accession><cross_references><pubmed>31969651</pubmed><doi>10.1038/s42003-020-0766-y</doi></cross_references></HashMap>