TY - JOUR KW - Cytokines KW - disease development KW - Household contact KW - leprosy KW - predictive marker AU - Oktaria S AU - Anfasa F AU - Menaldi S AU - Bramono K AU - Nijsten T AU - Thio H AB -
Background: Leprosy is a chronic infectious disease that can lead to severe lifelong disabilities. Close contacts of patients with leprosy have a higher risk of acquiring the disease. Nevertheless, there is a lack of reliable markers to predict infection. We aimed to identify new potential markers for developing clinical leprosy among contacts.
Methods: Serum levels of interleukin (IL) 6, IL-8, IL-10, hemoglobin, ferritin, and transferrin saturation were measured in 67 patients with multibacillary leprosy (MB), 65 household contacts (HHCs) of MB patients, and 127 endemic controls (ECs). By means of multivariate logistic regression and receiver operating characteristic (ROC) analyses, we analyzed baseline variables and laboratory parameters that showed significant differences between MB in the HHC and EC groups and obtained the respective areas under the curve (AUC). Optimal cutoff values of the associated cytokines were also determined.
Results: Elevated IL-6 level was observed in MB patients compared to HHCs and ECs ( = .022 and .0041, respectively). Anemia and iron deficiency were also higher in the MB group compared to HHCs or ECs ( < .001). Likewise, we observed an increased risk of having MB leprosy in underweight HHCs (odds ratio [OR], 2.599 [95% confidence interval {CI}, .991-6.820]) and underweight ECs (OR, 2.176 [95% CI, 1.010-4.692]). Further ROC analysis showed that high serum IL-6 level, underweight, anemia, and iron deficiency can discriminate leprosy from their HHCs (AUC, 0.843 [95% CI, .771-.914]; .000; optimal cutoff value of IL-6 = 9.14 pg/mL).
Conclusions: Our results suggest that serum IL-6 and nutrition status could serve as potential prognostic markers for the development of clinical leprosy in infected individuals.
BT - Open forum infectious diseases C1 -https://www.ncbi.nlm.nih.gov/pubmed/35237701
DA - 03/2022 DO - 10.1093/ofid/ofac010 IS - 3 J2 - Open Forum Infect Dis LA - eng N2 -Background: Leprosy is a chronic infectious disease that can lead to severe lifelong disabilities. Close contacts of patients with leprosy have a higher risk of acquiring the disease. Nevertheless, there is a lack of reliable markers to predict infection. We aimed to identify new potential markers for developing clinical leprosy among contacts.
Methods: Serum levels of interleukin (IL) 6, IL-8, IL-10, hemoglobin, ferritin, and transferrin saturation were measured in 67 patients with multibacillary leprosy (MB), 65 household contacts (HHCs) of MB patients, and 127 endemic controls (ECs). By means of multivariate logistic regression and receiver operating characteristic (ROC) analyses, we analyzed baseline variables and laboratory parameters that showed significant differences between MB in the HHC and EC groups and obtained the respective areas under the curve (AUC). Optimal cutoff values of the associated cytokines were also determined.
Results: Elevated IL-6 level was observed in MB patients compared to HHCs and ECs ( = .022 and .0041, respectively). Anemia and iron deficiency were also higher in the MB group compared to HHCs or ECs ( < .001). Likewise, we observed an increased risk of having MB leprosy in underweight HHCs (odds ratio [OR], 2.599 [95% confidence interval {CI}, .991-6.820]) and underweight ECs (OR, 2.176 [95% CI, 1.010-4.692]). Further ROC analysis showed that high serum IL-6 level, underweight, anemia, and iron deficiency can discriminate leprosy from their HHCs (AUC, 0.843 [95% CI, .771-.914]; .000; optimal cutoff value of IL-6 = 9.14 pg/mL).
Conclusions: Our results suggest that serum IL-6 and nutrition status could serve as potential prognostic markers for the development of clinical leprosy in infected individuals.
PY - 2022 EP - ofac010 T2 - Open forum infectious diseases TI - Serum Interleukin 6 Level and Nutrition Status as Potential Predictors of Clinical Leprosy Development Among Household Contacts in Endemic Areas. UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8883588/pdf/ofac010.pdf VL - 9 SN - 2328-8957 ER -