Evidence map›Paper›PMID 22944527›Full record

ArticleOsteoarthritis and cartilage2012

Serum non-coding RNAs as biomarkers for osteoarthritis progression after ACL injury.

L Zhang, M Yang, P Marks, L M White, M Hurtig, Q-S Mi, G Divine, G Gibson

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Osteoarthritis and cartilage, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Ribosome dysfunction in osteoarthritis.Current opinion in rheumatology · 2022
    Review
  10. Article
  11. Small Non-Coding RNAome of Ageing Chondrocytes.International journal of molecular sciences · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Non-Coding RNAs in Cartilage Development: An Updated Review.International journal of molecular sciences · 2019
    Review
  16. Epigenetics in osteoarthritis: Novel spotlight.Journal of cellular physiology · 2019
    Review
  17. Article
  18. Article
  19. Article
  20. 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

8 authors at 3 institutions in 2 countries.

L ZhangHenry Ford Hospital, Bone and Joint Center, 2799 West Grand Blvd., Detroit, MI 48202, United States. liangz_tkl@yahoo.com
M Yang
P Marks
L M White
M Hurtig
Q-S Mi
G Divine
G Gibson
Henry Ford Hospital · USUniversity of Toronto · CAUniversity of Guelph · CA

Funding

Serum microRNAs as biomarkers of post-traumatic osteoarthritisRC1AR058728 · NIAMS · HENRY FORD HEALTH SYSTEM · PI GIBSON, GARY J. · 2009 to 2010
$988k
CIHR ONT 68722NIAMS NIH HHS 5RC1AR58728-2NIAMS NIH HHS RC1 AR058728
6 · The paper itself

Abstract

objectiveThe aim of this study was to examine serum non-coding RNAs as potential biomarkers for cartilage damage associated with anterior cruciate ligament (ACL) injury.

methodsSerum was obtained from 80 patients 1 year after surgery for ACL injury and 60 normal donors without overt skeletal injury. Total serum RNA was isolated, small non-coding RNAs profiled by TaqMan array MicroRNA (miRNA) analysis and individual small RNA assays performed by quantitative TaqMan RT-PCR (qPCR). Semi-quantitative magnetic resonance imaging (MRI) analysis was performed using Whole Organ Magnetic Resonance Knee Score (WORMS) scoring for analysis of cartilage damage.

resultsInitial TaqMan array miRNA profiling showed an increased serum concentration of a small nucleolar RNA (snoRNA), U48, in five patients with cartilage damage compared with that in five patients without cartilage damage and six normal donors. Independent qPCR analysis of snoRNAs in serum from all patients and normal donors showed a strong association between the serum level of another snoRNA, U38, and cartilage damage in ACL injury patients and together with snoRNA, U48, clear distinction between ACL injury patients and normal donors.

conclusionSnoRNAs U38 and U48 are significantly elevated in the serum of patients developing cartilage damage at 1 year after ACL injury. Serum levels of U38 have the potential to facilitate early diagnosis of patients with cartilage damage after ACL injury. This study suggests serum non-coding RNAs may serve as novel noninvasive biomarkers for the detection and assessment of cartilage damage after ACL injury.

Indexed as

Anterior Cruciate Ligament InjuriesAdultAgedBiomarkersCartilage, ArticularDisease ProgressionFemaleHumansKnee InjuriesMagnetic Resonance ImagingMaleMiddle AgedOsteoarthritis, KneeReverse Transcriptase Polymerase Chain ReactionRNA, UntranslatedYoung AdultBiomarkersRNA, Untranslated

Identifiers

PMID22944527
PMCPMC3478481
OpenAlexW1968552646

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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.