Evidence map›Paper›PMID 42498942›Full record

ArticleImmunity & ageing : I & A2026

Reduced NK cell frequency in older patients with evolving fractures is linked to a distinct inflammatory cytokine profile.

Julia P Moch, Jolane Kappes, Rodrigo Gutierrez Jauregui, Hagen Schmaus, Malou-Sophie Dietrich, Daniel A Thies, Lennart M Roesner, Thomas Werfel, Reinhold Förster, Dorothee von Witzendorff and 8 more

Abstract read
In one paragraph

Article in Immunity & ageing : I & A, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Julia P MochCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Jolane KappesDepartment of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Carl-Neuberg-Straße 1, Hannover, Germany.
Rodrigo Gutierrez JaureguiCluster of Excellence RESIST (EXC 2155), Hannover Medical School, Hannover, Germany.
Hagen SchmausDepartment of Gastroenterology, Hepatology, Infectious Diseases and Endocrinology, Hannover Medical School, Carl-Neuberg-Straße 1, Hannover, Germany.
Malou-Sophie DietrichCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Daniel A ThiesCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Lennart M RoesnerCluster of Excellence RESIST (EXC 2155), Hannover Medical School, Hannover, Germany.
Thomas WerfelCluster of Excellence RESIST (EXC 2155), Hannover Medical School, Hannover, Germany.
Reinhold FörsterCluster of Excellence RESIST (EXC 2155), Hannover Medical School, Hannover, Germany.
Dorothee von WitzendorffCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Jennifer DebarryCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Marcel WinkelmannDepartment of Trauma Surgery, Hannover Medical School, Hannover, Germany.
Swantje OberthürDepartment of Trauma Surgery, Hannover Medical School, Hannover, Germany.
Jan-Dierk ClausenDepartment of Trauma Surgery, Hannover Medical School, Hannover, Germany.
Manfred GogolDepartment of Trauma Surgery, Hannover Medical School, Hannover, Germany.
Markus CornbergCentre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany.
Anke R M Kraft *Centre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany. Kraft.Anke@mh-hannover.de.
Christian Niehaus *Centre for Individualised Infection Medicine (CiiM), a joint venture between the Helmholtz Centre for Infection Research (HZI) and Hannover Medical School (MHH), Feodor-Lynen-Straße 7, Hannover, Germany. Niehaus.Christian@mh-hannover.de.ORCID http://orcid.org/0000-0003-0626-347X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProximal hip fractures represent a profound acute physiological stress in older adults and are often followed by infections, delayed recovery, and functional decline. These complications occur more frequently in frail individuals with reduced physiological resilience and impaired immune responses. As natural killer (NK) cells are central to early immune defense, we aimed to define how acute fracture, hospitalization and frailty shape NK cell homeostasis and function in older patients.

methodsWe conducted a prospective study including older patients (> 65 years) with acute fractures (SMART cohort; n = 103) and compared them to matched healthy older people from the RESIST senior individuals (SI) cohort (n = 550). A subset of SMART patients (n = 55) was longitudinally followed-up post-surgery. NK cell frequency, phenotype and function were investigated using multiparametric flow cytometry, and plasma soluble immune mediators (SIMs) were analyzed.

resultsSMART patients were clinically frailer than matched SI individuals, as indicated by reduced grip strength and lower Barthel scores, and exhibited an inflammatory state with elevated CRP levels and leukocyte counts. NK cell frequencies were significantly reduced in SMART patients and inversely correlated with grip strength and systemic inflammation. Furthermore, NK cells from SMART patients showed a distinct immune phenotype and altered chemokine receptor expression compared with SI individuals. Of note, differences between frail and non-frail patients within the SMART cohort were modest and substantially smaller than those observed between SMART patients and SI individuals. Functionally, frail patients displayed reduced baseline expression of cytotoxic molecules, whereas cytokine-induced NK cell responses were preserved. Furthermore, longitudinal analyses revealed stable NK cell frequencies but surgical intervention remodeled NK cell subset distribution and marker expression.

conclusionsIn conclusion, our findings indicate that NK cell alterations in older patients with fractures are likely driven by the combined impact of acute injury, hospitalization and surgery rather than by frailty alone.

Indexed as

Age-associated immune dysfunctionFracturesFrailtyNK cellsSoluble immune mediators

Identifiers

PMID42498942
PMCPMC13397730

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