Evidence map›Paper›PMID 40181286›Full record

ArticleBMC infectious diseases2025

Leptin and Iinterlukin-6 relationship and influence of mortality in sepsis.

Yi-Hsuan Tsai, Kai-Yin Hung, Wen-Feng Fang

Abstract read
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Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yi-Hsuan Tsai *Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Chang GungMemorial Hospital, Chang Gung University College of Medicine, Kaohsiung, 83301, Taiwan.
Kai-Yin Hung *Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Chang GungMemorial Hospital, Chang Gung University College of Medicine, Kaohsiung, 83301, Taiwan.
Wen-Feng FangDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kaohsiung Chang GungMemorial Hospital, Chang Gung University College of Medicine, Kaohsiung, 83301, Taiwan. fangwf@hotmail.com.

Funding

Kaohsiung Chang Gung Memorial Hospital CMRPG8K1671, CMRPG8B1063, CMRPG8B1063, CMRPG8J0422, CFRPG8H0431
6 · The paper itself

Abstract

backgroundSepsis is a severe and life-threatening disease involving multiple risk factors. Leptin has been suggested to play a role in modulating the inflammatory response in sepsis and improving outcomes; however, there are conflicting results regarding the outcome of sepsis. The present study aims to clarify the expression of leptin in patients with sepsis, and its association with other cytokines.

methodThe retrospective study enrolled 165 adults with sepsis from medical intensive care units (ICU)s, and collected leptin, glucose levels, and cytokines such as IL-6, IL-1RA, IL-10, IL-17, TNF-α, IFN-γfor analysis. Leptin levels were divided into three groups based on concentration: Low (≤ 3.78 ng/mL), Medium (3.78 < leptin ≤ 23.2 ng/mL), and High (> 23.2 ng/mL). Survival curve analysis and comparisons among groups were performed. A subgroup analysis by sex (male and female) was also conducted. Finally, a multiple-factor logistic regression model was used to evaluate the interaction between leptin and other factors.

resultThe high leptin groups were the oldest (low vs. medium vs. high: 60 vs. 66 vs. 78, p < 0.0001) and had the highest body mass index (BMI) (19.8 vs. 23.9 vs. 24.2, p < 0.0001), the highest percentages of women (28.6 vs. 34.1 vs. 65.9 p = 0.001), and the most comorbidities (1 vs. 1 vs. 2, p = 0.001). After controlling IL-6, day 1 leptin had a trend associated with lower mortality in the hospital (β = 0.984, p = 0.062). The highest IL-6 group had a significantly higher mortality rate among three IL-6 level patients (p = 0.015), but in the high leptin subgroup analysis, the significant effect of high IL-6 on mortality disappeared. Besides, the subgroup analysis of men, the high leptin group had a trend of better survival than the medium and low leptin groups.

conclusionHigh leptin levels may mitigate the adverse prognostic impact of elevated IL-6 on septic mortality. At comparable IL-6 levels, leptin could serve as a predictor of septic outcomes. Leptin might act as a protective factor in men. Future research should explore leptin's role in IL-6-mediated inflammation and its potential protective effect in high IL-6 sepsis cases.

Indexed as

Interleukin-6LeptinSepsisAdultAgedAged, 80 and overCytokinesFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesCytokinesIL6 protein, humanInterleukin-6LeptinInterleukin 6LeptinMortalitySepsis

Identifiers

PMID40181286
PMCPMC11966899

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.