Evidence map›Paper›PMID 37013608›Full record

ArticleJournal of translational medicine2023

Natural killer cytotoxicity in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): a multi-site clinical assessment of ME/CFS (MCAM) sub-study.

Troy D Querec, Jin-Mann S Lin, Yang Chen, Britany Helton, Andreas M Kogelnik, Nancy G Klimas, Daniel L Peterson, Lucinda Bateman, Charles Lapp, Richard N Podell and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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

13 authors at 6 institutions in 1 country.

Troy D QuerecDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA. hep0@cdc.gov.ORCID 0000-0002-3787-6271
Jin-Mann S LinDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Yang ChenDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Britany HeltonDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Andreas M KogelnikOpen Medicine Clinic, Mountain View, CA, USA.
Nancy G KlimasInstitute for Neuro Immune Medicine, Miami, FL, USA.
Daniel L PetersonSierra Internal Medicine, Incline Village, NV, USA.
Lucinda BatemanThe Bateman Horne Center, Salt Lake City, UT, USA.
Charles LappHunter-Hopkins Center, Charlotte, NC, USA.
Richard N PodellRichard N. Podell Medical, Summit, NJ, USA.
Benjamin H NatelsonDepartment of Neurology, Mount Sinai Beth Israel, New York, NY, USA.
Elizabeth R UngerDivision of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
MCAM Study Group
Centers for Disease Control and Prevention · USMount Sinai Beth Israel · USSierra Nevada College · USOpen Medicine Institute · USBateman Horne Center · USWashington Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a multisystem illness characterized by substantial reduction in function accompanied by profound unexplained fatigue not significantly relieved by rest, post-exertional malaise, and other symptoms. Reduced natural killer (NK) cell count and cytotoxicity has been investigated as a biomarker for ME/CFS, but few clinical laboratories offer the test and multi-site verification studies have not been conducted.

methodsWe determined NK cell counts and cytotoxicity in 174 (65%) ME/CFS, 86 (32%) healthy control (HC) and 10 (3.7%) participants with other fatigue associated conditions (ill control [IC]) from the Multi-Site Clinical Assessment of ME/CFS (MCAM) study using an assay validated for samples shipped overnight instead of testing on day of venipuncture.

resultsWe found a large variation in percent cytotoxicity [mean and (IQR) for ME/CFS and HC respectively, 34.1% (IQR 22.4-44.3%) and 33.6% (IQR 22.9-43.7%)] and no statistically significant differences between patients with ME/CFS and HC (p-value = 0.79). Analysis stratified on illness domain measured with standardized questionnaires did not identify an association of NK cytotoxicity with domain scores. Among all participants, NK cytotoxicity was not associated with survey results of physical and mental well-being, or health factors such as history of infection, obesity, smoking, and co-morbid conditions.

conclusionThese results indicate this assay is not ready for clinical implementation and studies are needed to further explore immune parameters that may be involved in the pathophysiology of ME/CFS.

Indexed as

Fatigue Syndrome, ChronicTRPM Cation ChannelsCD146 AntigenHumansKiller Cells, NaturalCD146 AntigenMCAM protein, humanTRPM Cation ChannelsComorbidityCytotoxicityMulticenter studyMultimorbidity (multiple medical conditions)Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)Natural killer cell (NK)

Identifiers

PMID37013608
PMCPMC10069115
OpenAlexW4362520735

What OpenQuestion holds

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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.