Evidence map›Paper›PMID 36836953›Full record

ArticleLife (Basel, Switzerland)2023

Determination of Heterogeneous Proteomic and Metabolomic Response in anti-TNF and anti-IL-6 Treatment of Patients with Rheumatoid Arthritis.

Alexander A Stepanov, Kristina A Malsagova, Arthur T Kopylov, Vladimir R Rudnev, Dmitry E Karateev, Evgenia I Markelova, Elena L Luchikhina, Elena E Borisova, Anna L Kaysheva

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2023. 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
1.7field-weighted citation impact, top 16% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Plasma proteome fingerprint in kidney diseases.Frontiers in molecular biosciences · 2024
    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

9 authors at 1 institution in 1 country.

Alexander A StepanovBiobanking Group, Branch of IBMC "Scientific and Education Center", 109028 Moscow, Russia.ORCID 0000-0002-9113-9440
Kristina A MalsagovaBiobanking Group, Branch of IBMC "Scientific and Education Center", 109028 Moscow, Russia.ORCID 0000-0001-9404-1660
Arthur T KopylovBiobanking Group, Branch of IBMC "Scientific and Education Center", 109028 Moscow, Russia.ORCID 0000-0002-7199-372X
Vladimir R RudnevBiobanking Group, Branch of IBMC "Scientific and Education Center", 109028 Moscow, Russia.
Dmitry E KarateevMoscow Regional Research and Clinical Institute ("MONIKI"), 129110 Moscow, Russia.
Evgenia I MarkelovaMoscow Regional Research and Clinical Institute ("MONIKI"), 129110 Moscow, Russia.
Elena L LuchikhinaMoscow Regional Research and Clinical Institute ("MONIKI"), 129110 Moscow, Russia.
Elena E BorisovaMoscow Regional Research and Clinical Institute ("MONIKI"), 129110 Moscow, Russia.
Anna L KayshevaBiobanking Group, Branch of IBMC "Scientific and Education Center", 109028 Moscow, Russia.ORCID 0000-0003-4472-2016
Moscow Regional Scientific Research Clinical Institute. MF Vladimirsky · RU

Funding

Russian Science Foundation 21-14-00381
6 · The paper itself

Abstract

Reduction in tumor necrosis factor (αTNF) and interleukin-6 (IL-6) activities is a widely utilized strategy for the treatment of rheumatoid arthritis (RA) with a high success rate. Despite both schemes targeting the deprivation of inflammatory reactions caused by the excessive activity of cytokines, their mechanisms of action and the final output are still unequal. This was a comparative longitudinal study that lasted for 24 weeks and aimed to find the answer to why the two schemes of therapy can pass out of proportion in attitude of their efficiency. What are the differences in metabolic and proteomic responses among patients who were being treated by either the anti-TNF or anti-IL-6 strategy? We found increased levels of immunoglobulins A and G (more than 2-fold in anti-IL-6 and more than 4-5-fold in anti-TNF groups) at the final stage (24 weeks) of monitoring but the most profound increase was determined for µ-chains of immunoglobulins in both groups of study. Metabolomic changes displayed main alterations with regard to arginine metabolism and collagen maintenance, where arginine increased 8.86-fold (

Indexed as

ELISAHPLC-MS/MSinhibitors of IL6inhibitors of TNFmetabolomeproteomerheumatoid arthritis

Identifiers

PMID36836953
PMCPMC9964360
OpenAlexW4321458173

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.