<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Wang TY</submitter><funding>Chang Gung Memorial Hospital, Linkou</funding><funding>National Center for Preparedness, Detection, and Control of Infectious Diseases</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>A regimen of once-weekly rifapentine plus isoniazid for 3 months (3HP) is an effective treatment for subjects with latent tuberculosis infection; however, no reliable biomarker exists for predicting systemic adverse reactions (SARs) to 3HP treatment.&lt;h4>Methods&lt;/h4>This prospective, multi-center study evaluated the plasma concentrations of soluble triggering receptors expressed on myeloid cells (sTREM)-1 and sTREM-2 in subjects undergoing 3HP treatment and examined the associations between these biomarkers and SARs.&lt;h4>Results&lt;/h4>This study enrolled 80 consecutive subjects receiving 3HP treatment, 25 of whom had SARs and 55 of whom did not. Subjects with SARs presented higher concentrations of sTREM-1 at baseline than those without SARs (240.1 ± 19.1 vs. 176.7 ± 9.4 pg/mL, &lt;i>P&lt;/i> = 0.001). The area under the receiver operating characteristic curves revealed that day 1 plasma levels of sTREM-1 (0.708, 95% CI, 0.584-0.833, &lt;i>P&lt;/i> = 0.003) and sTREM-2 (0.343, 95% CI, 0.227-0.459, &lt;i>P&lt;/i> = 0.025) as well as the sTREM-1/sTREM-2 ratio (0.748, 95% CI, 0.638-0.858, &lt;i>P&lt;/i> = 0.001) had modest discriminative power pertaining to the development of SARs. An sTREM-1 level exceeding the cut-off value (>187.4 pg/mL) (hazard ratio [HR], 6.15; 95% CI 1.67-22.70, &lt;i>P&lt;/i> = 0.006) and a sTREM-2 below the cut-off value (&lt;237.2 pg/mL) (HR, 4.46; 95% CI 1.41-14.1, &lt;i>P&lt;/i> = 0.011) were independent predictors of SARs after controlling for other variables.&lt;h4>Conclusions&lt;/h4>Plasma sTREM-1 and sTREM-2 levels are useful biomarkers for predicting SARs during 3HP treatment.&lt;h4>Clinical trial government&lt;/h4>NCT04655794.</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>821066</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8927064</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Plasma Concentrations of sTREM-1 as Markers for Systemic Adverse Reactions in Subjects Treated With Weekly Rifapentine and Isoniazid for Latent Tuberculosis Infection.</pubmed_title><pmcid>PMC8927064</pmcid><pubmed_authors>Shu CC</pubmed_authors><pubmed_authors>Wang TY</pubmed_authors><pubmed_authors>Chen CY</pubmed_authors><pubmed_authors>Lin SM</pubmed_authors><pubmed_authors>Lin CB</pubmed_authors><pubmed_authors>Su WJ</pubmed_authors><pubmed_authors>Wei YF</pubmed_authors><pubmed_authors>Lee SS</pubmed_authors><pubmed_authors>Feng JY</pubmed_authors><pubmed_authors>Huang WC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Plasma Concentrations of sTREM-1 as Markers for Systemic Adverse Reactions in Subjects Treated With Weekly Rifapentine and Isoniazid for Latent Tuberculosis Infection.</name><description>&lt;h4>Background&lt;/h4>A regimen of once-weekly rifapentine plus isoniazid for 3 months (3HP) is an effective treatment for subjects with latent tuberculosis infection; however, no reliable biomarker exists for predicting systemic adverse reactions (SARs) to 3HP treatment.&lt;h4>Methods&lt;/h4>This prospective, multi-center study evaluated the plasma concentrations of soluble triggering receptors expressed on myeloid cells (sTREM)-1 and sTREM-2 in subjects undergoing 3HP treatment and examined the associations between these biomarkers and SARs.&lt;h4>Results&lt;/h4>This study enrolled 80 consecutive subjects receiving 3HP treatment, 25 of whom had SARs and 55 of whom did not. Subjects with SARs presented higher concentrations of sTREM-1 at baseline than those without SARs (240.1 ± 19.1 vs. 176.7 ± 9.4 pg/mL, &lt;i>P&lt;/i> = 0.001). The area under the receiver operating characteristic curves revealed that day 1 plasma levels of sTREM-1 (0.708, 95% CI, 0.584-0.833, &lt;i>P&lt;/i> = 0.003) and sTREM-2 (0.343, 95% CI, 0.227-0.459, &lt;i>P&lt;/i> = 0.025) as well as the sTREM-1/sTREM-2 ratio (0.748, 95% CI, 0.638-0.858, &lt;i>P&lt;/i> = 0.001) had modest discriminative power pertaining to the development of SARs. An sTREM-1 level exceeding the cut-off value (>187.4 pg/mL) (hazard ratio [HR], 6.15; 95% CI 1.67-22.70, &lt;i>P&lt;/i> = 0.006) and a sTREM-2 below the cut-off value (&lt;237.2 pg/mL) (HR, 4.46; 95% CI 1.41-14.1, &lt;i>P&lt;/i> = 0.011) were independent predictors of SARs after controlling for other variables.&lt;h4>Conclusions&lt;/h4>Plasma sTREM-1 and sTREM-2 levels are useful biomarkers for predicting SARs during 3HP treatment.&lt;h4>Clinical trial government&lt;/h4>NCT04655794.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-06-18T06:01:13.596Z</modification><creation>2025-04-04T08:53:30.431Z</creation></dates><accession>S-EPMC8927064</accession><cross_references><pubmed>35308376</pubmed><doi>10.3389/fmicb.2022.821066</doi></cross_references></HashMap>