Evidence map›Paper›PMID 36013156›Full record

ArticleJournal of clinical medicine2022

The Role of

Raimonda Klimaitė, Mintautė Kazokaitė, Aistė Kondrotienė, Dalia Daukšienė, Rasa Sabaliauskaitė, Kristina Žukauskaitė, Birutė Žilaitienė, Sonata Jarmalaitė, Albertas Daukša

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. 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
0.4field-weighted citation impact, top 35% 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, 3 citations in OpenAlex.

  1. Article
  2. Association of DNA Promoter Methylation andCurrent oncology (Toronto, Ont.) · 2023
    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 3 institutions in 1 country.

Raimonda KlimaitėInstitute of Endocrinology, Medical Academy, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.ORCID 0000-0002-2351-8932
Mintautė KazokaitėInstitute of Endocrinology, Medical Academy, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.ORCID 0000-0002-8202-5484
Aistė KondrotienėInstitute of Endocrinology, Medical Academy, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.ORCID 0000-0002-9491-5599
Dalia DaukšienėInstitute of Endocrinology, Medical Academy, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.
Rasa SabaliauskaitėLaboratory of Genetic Diagnostic, National Cancer Institute, 50009 Vilnius, Lithuania.ORCID 0000-0002-3465-3558
Kristina ŽukauskaitėLaboratory of Genetic Diagnostic, National Cancer Institute, 50009 Vilnius, Lithuania.
Birutė ŽilaitienėInstitute of Endocrinology, Medical Academy, Lithuanian University of Health Sciences, 50009 Kaunas, Lithuania.ORCID 0000-0002-4082-4843
Sonata JarmalaitėLaboratory of Genetic Diagnostic, National Cancer Institute, 50009 Vilnius, Lithuania.
Albertas DaukšaInstitute of Digestive Research, Faculty of Medicine, Medical Academy, Lithuanian University of Health Sciences, 50161 Kaunas, Lithuania.
Lithuanian University of Health Sciences · LTVilnius University · LTNational Cancer Institute · LT

Funding

Lithuanian Research Council S-SEN-20-14
6 · The paper itself

Abstract

Aim: We investigated whether a difference exists between TSHR, PTEN and RASSF1A methylation status in plasma of subjects with papillary thyroid cancer (PTC). Methods: Peripheral blood samples were collected from 68 patients with PTC and 86 healthy controls (HC). Thyroid cancer tissue and corresponding adjacent normal tissue methylation levels were analyzed. DNA methylation level changes in TSHR, PTEN and RASSF1A genes were analyzed by quantitative methylation-sensitive polymerase chain reaction. Results: We observed that the methylation level of TSHR was significantly higher in the thyroid cancer tissue compared to adjacent normal tissue (p = 0.040). TSHR methylation levels in the PTC group plasma samples were significantly higher compared to HC (p = 0.022). After surgery, PTC plasma samples showed lower TSHR and PTEN methylation levels compared to the levels before surgery (p = 0.003, p = 0.031, respectively). The TSHR methylation level was significantly higher in PTC with larger tumor size (>2 cm) (p < 0.001), and lymph node metastases (p = 0.01), lymphovascular invasion (p = 0.02) and multifocality (p = 0.013) 0ROC analysis revealed that the TSHR methylation level provides high accuracy in distinguishing PTC from HC (p = 0.022, AUC of 0.616). Conclusion: TSHR methylation in peripheral blood samples is expected to be a sensitive and specific minimally invasive tool for the diagnosis of PTC, especially in combination with other diagnostic means.

Indexed as

methylationpapillary thyroid carcinomaPTCPTENRASSF1ATSHR

Identifiers

PMID36013156
PMCPMC9409956
OpenAlexW4292566372

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.