Evidence map›Paper›PMID 40866971›Full record

Observational studyCritical care (London, England)2025

Enhanced insights into immunity traits of elderly patients in the intensive care unit with infections: evidence from a multicenter, prospective observational study.

Ju Zou, Yuanyuan Xiao, Lina Zhang, Zhihong Zuo, Xianwen Wang, Xuelian Liao, Na Cui, Jialin Jin, Zhaoxin Qian, Anhua Wu and 1 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

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

11 authors.

Ju Zou *Department of Infection Control Center, Super drug-resistant Organism Infection Prevention and Control Research Center, Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Yuanyuan Xiao *Department of Infection Control Center, Super drug-resistant Organism Infection Prevention and Control Research Center, Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Lina Zhang *National Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Changsha, 410008, Hunan Province, China.
Zhihong ZuoNational Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Changsha, 410008, Hunan Province, China.
Xianwen WangNational Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Changsha, 410008, Hunan Province, China.
Xuelian LiaoDepartment of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Na CuiDepartment of Critical Care Medicine, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, 100730, China.
Jialin JinDepartment of Infectious Diseases, Shanghai Key Laboratory of Infectious Diseases and Biosafety Emergency Response, Shanghai Medical College, National Medical Center for Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, 200040, China.
Zhaoxin QianNational Clinical Research Center for Geriatric Disorders (Xiangya Hospital), Changsha, 410008, Hunan Province, China. xyqzx@csu.edu.cn.
Anhua WuDepartment of Infection Control Center, Super drug-resistant Organism Infection Prevention and Control Research Center, Xiangya Hospital, Central South University, Changsha, Hunan Province, China. xywuanhua@csu.edu.cn.
Chunhui LiDepartment of Infection Control Center, Super drug-resistant Organism Infection Prevention and Control Research Center, Xiangya Hospital, Central South University, Changsha, Hunan Province, China. lichunhui@csu.edu.cn.

Funding

Innovation and Technology Commercialization Fund of Xiangya Hospital, Central South University 2024ZHJJ06Scientific and Technological Personnel Lifting Project in Hunan Province 2023TJ-Z11the National Key Research and Development Program of China 2022YFC2009801the National Key Research and Development Program of China 2022YFC2009805the National Natural Science Foundation of China -China State Railway Group Co., Ltd. Railway Fundamental Research Joint Fund U2368213
6 · The paper itself

Abstract

backgroundInfections, particularly sepsis, are a global health threat and a leading cause of mortality among elderly patients (≥ 60 years) in intensive care units (ICUs). The variable immune responses in this vulnerable population warrant deeper investigation.

methodsThis multicenter prospective study included elderly patients with infections admitted to the ICUs of four hospitals between May 2023 and October 2024. Patients were classified into sepsis and non-sepsis infection groups based on a ≥2-point increase in Sequential Organ Failure Assessment (SOFA) score. Baseline immune and inflammatory markers were compared between groups. Logistic regression analyses were used to assess associations with mortality. Subgroup analyses were conducted by sex, age, infection site, and pathogen type.

resultsAmong 1,152 elderly patients with infections in the ICUs, 640 with sepsis were older (70.0 vs.72.0 years), were predominantly male (55.3% vs. 68.1%), and had more comorbidities, all P < 0.001. Compared with the non-sepsis infection group, the septic group had higher rates of mechanical ventilation (3.12% vs. 40.80%), longer hospitalization (7.00 [4.00;10.0] vs. 11.8 [6.00;18.0] days), and increased mortality (0.98% vs. 9.51%), all P < 0.001. Distinct immune-mortality signatures were observed. In the fully adjusted model, non-septic infection was associated with reduced monocytes, lymphocytes, and TNFα (odds ratio [OR] < 1), elevated interleukin-12 (IL12) and INFγ (OR > 1, all P < 0.05), whereas sepsis was characterized by increased neutrophil and B-cell activation (OR > 1), decreased T cells (OR < 1, all P < 0.05), and no specific cytokine signature (all P > 0.05). Sex differences included higher levels of innate immune markers in males and elevated adaptive immune indicators in females. With age, patients showed reduced T cell counts and increased inflammatory markers (procalcitonin and C-reactive protein). Patients aged > 80 years exhibited marked lymphopenia, lower CD4

conclusionsElderly patients in the ICU, especially those with sepsis, exhibit immune imbalances of hyperinflammation and immunosuppression, varying with age, sex, pathogen type, and infection site. These findings highlight the potential role of immune phenotyping in guiding treatment decisions in this patient population.

Indexed as

InfectionsAgedAged, 80 and overFemaleHumansIntensive Care UnitsLogistic ModelsMaleOrgan Dysfunction ScoresProspective StudiesSepsisElderlyImmune responseImmunosenescenceInfectionSepsis

Identifiers

PMID40866971
PMCPMC12392643

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.