Evidence map›Paper›PMID 28811623›Full record

ArticleScientific reports2017

Immune dysregulation in patients with carpal tunnel syndrome.

Gila Moalem-Taylor, Benny Baharuddin, Barbara Bennett, Arun V Krishnan, William Huynh, Matthew C Kiernan, Cindy Shin-Yi Lin, Boaz Shulruf, Elizabeth Keoshkerian, Barbara Cameron and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 20% of its field
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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Gila Moalem-TaylorSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia. gila@unsw.edu.au.ORCID 0000-0003-3828-9527
Benny BaharuddinSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Barbara BennettSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Arun V KrishnanPrince of Wales Clinical School, University of New South Wales UNSW Australia, Sydney, NSW 2031, Australia.
William HuynhPrince of Wales Clinical School, University of New South Wales UNSW Australia, Sydney, NSW 2031, Australia.
Matthew C KiernanBrain and Mind Centre, Sydney Medical School, The University of Sydney, and Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
Cindy Shin-Yi LinSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Boaz ShulrufSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Elizabeth KeoshkerianThe Kirby Institute, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Barbara CameronSchool of Medical Sciences, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
Andrew LloydThe Kirby Institute, University of New South Wales UNSW Australia, Sydney, NSW 2052, Australia.
UNSW Sydney · AUThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral immunity plays a key role in maintaining homeostasis and conferring crucial neuroprotective effects on the injured nervous system, while at the same time may contribute to increased vulnerability to neuropathic pain. Little is known about the reciprocal relationship between entrapment neuropathy and peripheral immunity. This study investigated immune profile in patients with carpal tunnel syndrome (CTS), the most prevalent entrapment neuropathy. All patients exhibited neurophysiological abnormalities in the median nerve, with the majority reporting neuropathic pain symptoms. We found a significant increase in serum CCL5, CXCL8, CXCL10 and VEGF, and in CD4+ central and effector memory T cells in CTS patients, as compared to healthy controls. CCL5 and VEGF were identified as having the highest power to discriminate between patients and controls. Interestingly, and contrary to the prevailing view of CCL5 as a pro-nociceptive factor, the level of circulating CCL5 was inversely correlated with neuropathic pain intensity and median nerve motor latency. In contrast, the level of central memory T cells was positively associated with abnormal neurophysiological findings. These results suggest that entrapment neuropathy is associated with adaptive changes in the homeostasis of memory T cells and an increase in systemic inflammatory modulating cytokines/chemokines, which potentially regulate neuropathic symptoms.

Indexed as

ImmunityAdultAgedBiomarkersCarpal Tunnel SyndromeCytokinesFemaleHumansImmunologic MemoryLymphocyte CountMaleMiddle AgedRisk FactorsSymptom AssessmentT-Lymphocyte SubsetsBiomarkersCytokines

Identifiers

PMID28811623
PMCPMC5557984
OpenAlexW2743268753

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.