Evidence map›Paper›PMID 27676445›Full record

ArticleTranslational psychiatry2016

Bottom-up proteomics suggests an association between differential expression of mitochondrial proteins and chronic fatigue syndrome.

F Ciregia, L Kollipara, L Giusti, R P Zahedi, C Giacomelli, M R Mazzoni, G Giannaccini, P Scarpellini, A Urbani, A Sickmann and 2 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 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

12 authors at 3 institutions in 2 countries.

F CiregiaDepartment of Pharmacy, University of Pisa, Pisa, Italy.
L KolliparaLeibniz-Institut für Analytische Wissenschaften-ISAS, Dortmund, Germany.
L GiustiDepartment of Pharmacy, University of Pisa, Pisa, Italy.
R P ZahediLeibniz-Institut für Analytische Wissenschaften-ISAS, Dortmund, Germany.
C GiacomelliDivision of Rheumatology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
M R MazzoniDepartment of Pharmacy, University of Pisa, Pisa, Italy.
G GiannacciniDepartment of Pharmacy, University of Pisa, Pisa, Italy.
P ScarpelliniDivision of Psychiatry, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
A UrbaniIstituto di Biochimica e Biochimica Clinica, Università Cattolica, Rome, Italy.
A SickmannLeibniz-Institut für Analytische Wissenschaften-ISAS, Dortmund, Germany.
A LucacchiniDepartment of Pharmacy, University of Pisa, Pisa, Italy.
L BazzichiDivision of Rheumatology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
University of Pisa · ITLeibniz Institute for Analytical Sciences - ISAS · DEFondazione Santa Lucia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic fatigue syndrome (CFS) is a debilitating and complex disorder characterized by unexplained fatigue not improved by rest. An area of investigation is the likely connection of CFS with defective mitochondrial function. In a previous work, we investigated the proteomic salivary profile in a couple of monozygotic twins discordant for CFS. Following this work, we analyzed mitochondrial proteins in the same couple of twins. Nano-liquid chromatography electrospray ionization mass spectrometry (nano-LC-MS) was used to study the mitochondria extracted from platelets of the twins. Subsequently, we selected three proteins that were validated using western blot analysis in a big cohort of subjects (n=45 CFS; n=45 healthy), using whole saliva (WS). The selected proteins were as follows: aconitate hydratase (ACON), ATP synthase subunit beta (ATPB) and malate dehydrogenase (MDHM). Results for ATPB and ACON confirmed their upregulation in CFS. However, the MDHM alteration was not confirmed. Thereafter, seeing the great variability of clinical features of CFS patients, we decided to analyze the expression of our proteins after splitting patients according to clinical parameters. For each marker, the values were actually higher in the group of patients who had clinical features similar to the ill twin. In conclusion, these results suggest that our potential markers could be one of the criteria to be taken into account for helping in diagnosis. Furthermore, the identification of biomarkers present in particular subgroups of CFS patients may help in shedding light upon the complex entity of CFS. Moreover, it could help in developing tailored treatments.

Identifiers

PMID27676445
PMCPMC5048217
OpenAlexW2527491610

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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.