<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Visconti VV</submitter><funding>INAIL-BRIC</funding><funding>MIUR-PRIN</funding><pagination>288</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8086331</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The long pentraxin PTX3 is generating great interest given the recent discovery of its involvement in bone metabolism. This study investigates the role of circulating PTX3 as a marker of bone-related phenotypes in patients with osteoporosis (OP) and osteoarthritis (OA).&lt;h4>Methods&lt;/h4>Serum PTX3 levels were determined using an enzyme-linked immunosorbent assay (ELISA) in a total of OP (n=32), OA (n=19) patients and healthy controls (CTR; n=25). ROC curve analysis was carried out to evaluate the potential of PTX3 for the diagnosis of bone-related phenotypes. In addition, the association between PTX3 serum levels and biochemical markers was estimated by Spearman correlation analysis.&lt;h4>Results&lt;/h4>Serum analysis reveals a statistically significant increase of PTX3 levels in OP and OA patients, compared to CTR subjects (**** p &lt; 0.0001, **** p &lt; 0.0001). ROC curve of PTX3 levels exhibits an excellent sensitivity and specificity for OP and OA diseases (**** p &lt; 0.0001 and **** p &lt; 0.0001, respectively). Moreover, serum PTX3 levels are positively associated with ALP (r = - 0.5257, p = 0.0083) and PTH levels (r = 0.4704, p = 0.0203) in OP patients.&lt;h4>Conclusions&lt;/h4>These results confirm the pivotal role of PTX3 in bone metabolism and suggest its potential use as a predictor of OP and OA bone-related phenotypes.</pubmed_abstract><journal>Journal of orthopaedic surgery and research</journal><pubmed_title>The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes.</pubmed_title><pmcid>PMC8086331</pmcid><funding_grant_id>2019#23</funding_grant_id><funding_grant_id>201528E7CM</funding_grant_id><pubmed_authors>Tallarico M</pubmed_authors><pubmed_authors>Casamassima D</pubmed_authors><pubmed_authors>Romano F</pubmed_authors><pubmed_authors>Visconti VV</pubmed_authors><pubmed_authors>Tarantino U</pubmed_authors><pubmed_authors>Fittipaldi S</pubmed_authors><pubmed_authors>Botta A</pubmed_authors><pubmed_authors>Greggi C</pubmed_authors></additional><is_claimable>false</is_claimable><name>The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes.</name><description>&lt;h4>Background&lt;/h4>The long pentraxin PTX3 is generating great interest given the recent discovery of its involvement in bone metabolism. This study investigates the role of circulating PTX3 as a marker of bone-related phenotypes in patients with osteoporosis (OP) and osteoarthritis (OA).&lt;h4>Methods&lt;/h4>Serum PTX3 levels were determined using an enzyme-linked immunosorbent assay (ELISA) in a total of OP (n=32), OA (n=19) patients and healthy controls (CTR; n=25). ROC curve analysis was carried out to evaluate the potential of PTX3 for the diagnosis of bone-related phenotypes. In addition, the association between PTX3 serum levels and biochemical markers was estimated by Spearman correlation analysis.&lt;h4>Results&lt;/h4>Serum analysis reveals a statistically significant increase of PTX3 levels in OP and OA patients, compared to CTR subjects (**** p &lt; 0.0001, **** p &lt; 0.0001). ROC curve of PTX3 levels exhibits an excellent sensitivity and specificity for OP and OA diseases (**** p &lt; 0.0001 and **** p &lt; 0.0001, respectively). Moreover, serum PTX3 levels are positively associated with ALP (r = - 0.5257, p = 0.0083) and PTH levels (r = 0.4704, p = 0.0203) in OP patients.&lt;h4>Conclusions&lt;/h4>These results confirm the pivotal role of PTX3 in bone metabolism and suggest its potential use as a predictor of OP and OA bone-related phenotypes.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2026-05-08T07:04:25.835Z</modification><creation>2025-04-05T21:36:57.2Z</creation></dates><accession>S-EPMC8086331</accession><cross_references><pubmed>33931080</pubmed><doi>10.1186/s13018-021-02440-3</doi></cross_references></HashMap>