The Diagnostic and prognostic value of CXCL12 (SDF-1α) level in Mycobacterium tuberculosis infection and disease.
Autor: | Koca Kalkan I; Department of Allergy and Clinical Immunology, Ataturk Chest Disease and Thoracic Surgery Training and Research Hospital, Ankara, Turkey. ilkay.koca@gmail.com., Gozu A; Department of Pulmonology, Ataturk Chest Disease and Thoracic Surgery Training and Research Hospital, Ankara, Turkey., Tansel E; Department of Pulmonology, Ataturk Chest Disease and Thoracic Surgery Training and Research Hospital, Ankara, Turkey., Kalac SN; Department of Pulmonology, Ataturk Chest Disease and Thoracic Surgery Training and Research Hospital, Ankara, Turkey., Samurkasoglu B; Department of Pulmonology, Ataturk Chest Disease and Thoracic Surgery Training and Research Hospital, Ankara, Turkey., Simsek H; Department of Medical Microbiology, Yozgat Bozok University Faculty of Medicine, Yozgat, Turkey. |
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Jazyk: | angličtina |
Zdroj: | Journal of infection in developing countries [J Infect Dev Ctries] 2021 Jan 31; Vol. 15 (1), pp. 81-88. Date of Electronic Publication: 2021 Jan 31. |
DOI: | 10.3855/jidc.12989 |
Abstrakt: | Introduction: New diagnostic tools are being investigated for rapid and accurate TB detection. We aimed to find out the diagnostic yield and accuracy of chemokine CXCL12 (SDF-1a) levels in diagnosing active TB (aTB) and making a differential diagnosis from other several infectious/non-infectious pulmonary conditions. Methodology: We collected demographic, clinic features and studied plasma CXCL12 levels using ELISA kit of the participants, classified into five categories: aTB (n = 30); cured TB (cTB, n = 15); close contacts of aTB (CC, n = 15); chronic obstructive pulmonary disease (COPD) with active nonspecific pulmonary infection (infCOPD, n = 15); and healthy controls (HC, n = 15). Results: CXCL12 levels were highest in aTB, but no significant difference was seen between other groups. When a cut-off level for CXCL12 was determined as 2835 pg/mL, the increased CXCL12 rate was significantly more in aTB than CC and HC (p = 0.02, p = 0.05). Also, participants with an active infection (aTB and infCOPD) had significantly higher increased CXCL12 rates (p = 0.01). The sensitivity and specificity of CXCL12 for diagnosing aTB were found to be 0.56 and 0.63, respectively. We found that bacterial load, the radiological severity and the extent of chest x-ray involvement were independent factors for increased CXCL12 levels. Conclusions: Our study demonstrates that CXCL12 may be a representative of active pulmonary infection regardless of the cause but correlated with the severity of the disease; enabling this test to be used as a prognostic factor rather than a diagnostic test for aTB. Competing Interests: No Conflict of Interest is declared (Copyright (c) 2021 Ilkay Koca Kalkan, Ayse Gozu, Ebru Tansel, Serife Nilgun Kalac, Belgin Samurkasoglu, Hulya Simsek.) |
Databáze: | MEDLINE |
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