Evidence map›Paper›PMID 40247243›Full record

Observational studyBMC musculoskeletal disorders2025

Role of IL-16 in age-related skeletal muscle atrophy: an integrated study.

Wenliang Fan, Zhibang Zhao, Liqiang Wang, Qingbo Chu

Abstract readObservational Study
In one paragraph

Observational study in BMC musculoskeletal disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

4 authors.

Wenliang FanEmergency Trauma Center, Nanyang Second People's Hospital, No 66, East Jianshe Road, Nanyang, 473000, Henan, China.
Zhibang ZhaoEmergency Trauma Center, Nanyang Second People's Hospital, No 66, East Jianshe Road, Nanyang, 473000, Henan, China.
Liqiang WangEmergency Trauma Center, Nanyang Second People's Hospital, No 66, East Jianshe Road, Nanyang, 473000, Henan, China.
Qingbo ChuEmergency Trauma Center, Nanyang Second People's Hospital, No 66, East Jianshe Road, Nanyang, 473000, Henan, China. 13721809268@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn this study, we aim to explore the roles of IL-16 in sarcopenia based on older orthopedic patients and animal research.

methodsThis clinical research in this study was an observational investigation and included all the older patients with orthopedic trauma admitted to our department between January 2021 and January 2022. Patients were identified with sarcopenia if they have both low hand grip strength (HGS) and low appendicular skeletal muscle mass (ASM). Propensity score matching (PSM) was performed to reduce the bias caused by the co-factors and levels of IL-16 between normal patients and patients with sarcopenia were compared. In animal research, mice were treated with IL-16 to identify the effects of IL-16 on muscle function and muscle mass. Then the sarcopenia models were established and the anti-IL-16 was performed to identify the potential therapeutical effect of targeting IL-16.

results421 individuals were included in the clinical study, and 77 were identified as sarcopenia. In the matched populations, the serum levels of IL-16 of individuals with low HGS, ASM, and sarcopenia were significantly higher than normal individuals (all p < 0.001). The mice treated with IL-16 showed significantly impaired muscle function and physical performance and loss of muscle mass. Using anti-IL-16 antibodies may rescue the sarcopenia traits caused by botulinum toxin type A.

conclusionIndividuals with high levels of IL-16 may have a significantly high risk of sarcopenia. IL-16 impairs muscle function and physical performance and leads to muscle atrophy in mice, and these effects could be reduced by targeting IL-16.

Indexed as

AgingInterleukin-16Muscle, SkeletalMuscular AtrophySarcopeniaAgedAged, 80 and overAnimalsDisease Models, AnimalFemaleHand StrengthHumansMaleMiceMice, Inbred C57BLInterleukin-16CytokinesIL-16InflammagingMuscle atrophySarcopenia

Identifiers

PMID40247243
PMCPMC12004841

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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.