Efficacy of zinc supplementation on serum calprotectin, inflammatory cytokines and outcome in neonatal sepsis - a randomized controlled trial

被引:35
作者
Banupriya, Newton [1 ]
Bhat, Ballambattu Vishnu [1 ]
Benet, Bosco Dhas [1 ]
Sridhar, Magadi Gopalakrishna [2 ]
Parija, Subhash Chandra [3 ]
机构
[1] Jawaharlal Inst Postgrad Med Educ & Res, Dept Neonatol, Pondicherry 605006, India
[2] Jawaharlal Inst Postgrad Med Educ & Res, Dept Biochem, Pondicherry 605006, India
[3] Jawaharlal Inst Postgrad Med Educ & Res, Dept Microbiol, Pondicherry 605006, India
关键词
Newborns; zinc; ELISA; biomarkers; mortality; PLACEBO-CONTROLLED-TRIAL; ANTIMICROBIAL ACTIVITY; DOUBLE-BLIND; MORTALITY; PROTEINS;
D O I
10.1080/14767058.2016.1220524
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To find out the efficacy of zinc supplementation in decreasing the levels of serum calprotectin and inflammatory cytokines with improvement in outcome in neonatal sepsis. Methods: Neonates with clinical signs suggestive of sepsis and at least two screening tests positive were randomized into two groups - zinc group and control group. The zinc group received 3 mg/kg of zinc sulfate monohydrate twice a day orally for 10 days along with antibiotics. The control group received antibiotics and supportive care. Serum zinc, calprotectin, TNF-alpha and IL-6 were estimated in serum at recruitment and 10 days later after completion of antibiotics. The babies were monitored daily till discharge and mortality rate was compared between the groups. Results: Baseline characteristics were similar between the groups. Serum zinc levels were considerably increased in the zinc group after supplementation. There was significant decline in concentrations of serum calprotectin, TNF-alpha and IL-6 (p < 0.05) in the zinc group. In the control group also, serum calprotectin and IL-6 levels were found to be decreased significantly after antibiotic treatment (p < 0.05), while TNF-alpha showed insignificant reduction. Kaplan-Meier analysis was performed to assess the survival time between the groups. The mortality was lower in the zinc group compared to the control group 5 versus 11, p = 0.12. Conclusion: Neonates with sepsis who received zinc in addition to antibiotics showed significant reduction in serum calprotectin and inflammatory cytokines. Although mortality was lower in zinc group, it was not statistically significant.
引用
收藏
页码:1627 / 1631
页数:5
相关论文
共 25 条
[1]  
Abdel-Maaboud M, 2012, EGYPT J PEDIATR ALLE, V10, P19
[2]   Zinc as adjunct treatment in infants aged between 7 and 120 days with probable serious bacterial infection: a randomised, double-blind, placebo-controlled trial [J].
Bhatnagar, Shinjini ;
Wadhwa, Nitya ;
Aneja, Satinder ;
Lodha, Rakesh ;
Kabra, Sushil Kumar ;
Natchu, Uma Chandra Mouli ;
Sommerfelt, Halvor ;
Dutta, Ashok Kumar ;
Chandra, Jagdish ;
Rath, Bimbadhar ;
Sharma, Mamta ;
Sharma, Vinod Kumar ;
Kumari, Mohini ;
Strand, Tor A. .
LANCET, 2012, 379 (9831) :2072-2078
[3]   CALPROTECTIN-MEDIATED ZINC CHELATION AS A BIOSTATIC MECHANISM IN HOST-DEFENSE [J].
CLOHESSY, PA ;
GOLDEN, BE .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 42 (05) :551-556
[4]   His-X-X-X-His motif in S100 protein, calprotectin: Relation to microbiostatic activity [J].
Clohessy, PA ;
Golden, BE .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (05) :674-674
[5]   Sepsis: Links between pathogen sensing and organ damage [J].
Crouser, Elliott ;
Exline, Matthew ;
Knoell, Daren ;
Wewers, Mark D. .
CURRENT PHARMACEUTICAL DESIGN, 2008, 14 (19) :1840-1852
[6]  
Dhas D. B. B., 2012, Current Pediatric Research, V16, P83
[7]   Functions of S100 Proteins [J].
Donato, R. ;
Cannon, B. R. ;
Sorci, G. ;
Riuzzi, F. ;
Hsu, K. ;
Weber, D. J. ;
Geczy, C. L. .
CURRENT MOLECULAR MEDICINE, 2013, 13 (01) :24-57
[8]   Zinc and Regulation of Inflammatory Cytokines: Implications for Cardiometabolic Disease [J].
Foster, Meika ;
Samman, Samir .
NUTRIENTS, 2012, 4 (07) :676-694
[9]  
Ghaliyah A.Z., 2015, INT J SCI RES, V4, P311
[10]   Histidine-based zinc-binding sequences and the antimicrobial activity of calprotectin [J].
Loomans, HJ ;
Hahn, BL ;
Li, QQ ;
Phadnis, SH ;
Sohnle, PG .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (03) :812-814