Evidence map›Paper›PMID 32472302›Full record

ArticleRheumatology international2020

Autoantibodies against a novel citrullinated fibrinogen peptide related to smoking status, disease activity and therapeutic response to methotrexate in cuban patients with early rheumatoid arthritis.

Goitybell Martínez, Eugen Feist, Maité Martiatu, Hilda Garay, Bárbara Torres

Abstract read
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In one paragraph

Article in Rheumatology international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. The influence of smoking on the efficacy of a single-dose methotrexate treatment for ectopic pregnancy.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2025
    Article
  2. 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

5 authors at 2 institutions in 2 countries.

Goitybell MartínezImmunology Laboratory, National Center of Medical Genetic, Havana, Cuba. goity@infomed.sld.cu.ORCID http://orcid.org/0000-0002-6679-1410
Eugen FeistDepartment for Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany.ORCID http://orcid.org/0000-0002-9872-5282
Maité MartiatuImmunology Laboratory, National Center of Medical Genetic, Havana, Cuba.ORCID http://orcid.org/0000-0002-0117-4665
Hilda GarayCenter of Genetic Engineering and Biotechnology, Havana, Cuba.ORCID http://orcid.org/0000-0003-3101-255X
Bárbara TorresImmunology Laboratory, National Center of Medical Genetic, Havana, Cuba.ORCID http://orcid.org/0000-0001-9729-5172
Centro de Ingeniería Genética y Biotecnología · CUHelios Hospital Schwerin · DE

Funding

National Center of Medical Genetic. Ministry of Health 13-99-001
6 · The paper itself

Abstract

Treatment recommendations of early rheumatoid arthritis (RA) suggest differential management of patients on the basis of prognostic factors. In this study we aimed to investigate the relationship between autoantibodies against a novel citrullinated fibrinogen peptide (anti-CFP), smoking status, clinical activity and therapeutic response in Cuban patients with early RA, receiving treatment with methotrexate in comparison to rheumatoid factor (RF), anti-cyclic citrullinated peptide of second generation (anti-CCP2) and anti-mutated citrullinated vimentin (anti-MCV). A 6-month prospective observational study was performed in 60 early RA patients at baseline and 6 months after receiving methotrexate. Baseline and outcome measures included disease activity score of 28 joints (DAS 28), simplified disease activity index (SDAI), anti-CFP antibodies, RF, anti-CCP2 and anti-MCV. Therapeutic response was determined using 20/50/70 American College of Rheumatology (ACR) response rates. DAS28 (p < 0.0001), SDAI (p < 0.0001) as well as titres of anti-CFP (p = 0.0481), anti-CCP2 (p = 0.0082), RF IgM (p = 0.0187) and RF IgA (p = 0.0252) decreased under therapy. Multivariate analyses showed association of final anti-CFP values with sex and smoking status (p = 0.0296). It is of note that anti-CFP antibodies were one of predictors for DAS 28 (p = 0.0072) SDAI (p < 0.0001) and ACR response (p = 0.0003) in multivariate models. Anti-CFP antibodies decrease in correspondence with clinical improvement after 6-month therapy and are associated with sex and smoking status. Moreover, baseline anti-CFP antibodies, using in combination with sex, smoking status and autoantibodies (anti-CCP2, anti-MCV or RF) seems to have clinical relevance for predicting clinical activity and therapeutic response.

Indexed as

AdultAnti-Citrullinated Protein AntibodiesAntirheumatic AgentsArthritis, RheumatoidCubaEnzyme-Linked Immunosorbent AssayFemaleFibrinogenHumansMaleMethotrexateMiddle AgedSeverity of Illness IndexSmokingTreatment OutcomeAnti-Citrullinated Protein AntibodiesAntirheumatic AgentsFibrinogenMethotrexateAntibodiesClinical activityMethotrexateRheumatoid arthritisSmoking

Identifiers

PMID32472302
OpenAlexW3030814245

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.