Evidence map›Paper›PMID 38790038›Full record

ArticleArthritis research & therapy2024

Two-year post-distraction cartilage-related structural improvement is accompanied by increased serum full-length SIRT1.

Miya Marco, Mylène Jansen, Goran van der Weiden, Eli Reich, Yonathan H Maatuf, Simon C Mastbergen, Mona Dvir-Ginzberg

Abstract read
In one paragraph

Article in Arthritis research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. 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

7 authors.

Miya MarcoLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hadassah-Hebrew University of Jerusalem, P. O. Box 12272, Jerusalem, 9112102, Israel.
Mylène JansenRheumatology & Clinical Immunology, University Utrecht, University Medical Center Utrecht, Utrecht, The Netherlands.
Goran van der WeidenRheumatology & Clinical Immunology, University Utrecht, University Medical Center Utrecht, Utrecht, The Netherlands.
Eli ReichLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hadassah-Hebrew University of Jerusalem, P. O. Box 12272, Jerusalem, 9112102, Israel.
Yonathan H MaatufLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hadassah-Hebrew University of Jerusalem, P. O. Box 12272, Jerusalem, 9112102, Israel.
Simon C MastbergenRheumatology & Clinical Immunology, University Utrecht, University Medical Center Utrecht, Utrecht, The Netherlands.
Mona Dvir-GinzbergLaboratory of Cartilage Biology, Institute of Bio-Medical and Oral Research, Faculty of Dental Medicine, Hadassah-Hebrew University of Jerusalem, P. O. Box 12272, Jerusalem, 9112102, Israel. Mona.Dvir-Ginzberg@mail.huji.ac.il.

Funding

Dutch Arthritis Society NR 17 - 02 - 405 and LLP9EU FP7; HEALTH.2012.2.4.5-2 305815Israel Science Foundation 121/12, 370/17Ministry of Science and Technology, Israel 3-17335Rosetrees Trust A770
6 · The paper itself

Abstract

backgroundPreviously, fragments from Sirtuin 1 (SIRT1) were identified in preclinical and clinical samples to display an increase in serum levels for N-terminal (NT) SIRT1 vs. C-terminal (CT) SIRT1, indicative of early signs of OA. Here we tested NT/CT SIRT1 levels as well as a novel formulated sandwich assay to simultaneously detect both domains of SIRT1 in a manner that may inform us about the levels of full-length SIRT1 in the circulation (flSIRT1) of clinical cohorts undergoing knee joint distraction (KJD).

methodsWe employed an indirect ELISA assay to test NT- and CT-SIRT1 levels and calculated their ratio. Further, to test flSIRT1 we utilized novel antibodies (Ab), which were validated for site specificity and used in a sandwich ELISA method, wherein the CT-reactive served as capture Ab, and its NT-reactive served as primary detection Ab. This method was employed in human serum samples derived from a two-year longitudinal study of KJD patients. Two-year clinical and structural outcomes were correlated with serum levels of flSIRT1 compared to baseline.

resultsAssessing the cohort, exhibited a significant increase of NT/CT SIRT1 serum levels with increased osteophytes and PIIANP/CTX-II at baseline, while a contradictory increase in NT/CT SIRT1 was associated with less denuded bone, post-KJD. On the other hand, flSIRT1 exhibited an upward trend in serum level, accompanied by reduced denuded bone for 2-year adjusted values. Moreover, 2 year-adjusted flSIRT1 levels displayed a steeper linear regression for cartilage and bone-related structural improvement than those observed for NT/CT SIRT1.

conclusionsOur data support that increased flSIRT1 serum levels are a potential molecular endotype for cartilage-related structural improvement post-KJD, while NT/CT SIRT1 appears to correlate with osteophyte and PIIANP/CTX-II reduction at baseline, to potentially indicate baseline OA severity.

Indexed as

Osteoarthritis, KneeSirtuin 1AdultAgedBiomarkersCartilage, ArticularEnzyme-Linked Immunosorbent AssayFemaleHumansKnee JointLongitudinal StudiesMaleMiddle AgedBiomarkersSIRT1 protein, humanSirtuin 1ELISAEndotypeFull-length Sirt1Joint distractionOsteoarthritisSerum biomarker

Identifiers

PMID38790038
PMCPMC11127335

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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.