Evidence map›Paper›PMID 23259706›Full record

ArticleThyroid : official journal of the American Thyroid Association2013

Measurement of calcitonin and calcitonin gene-related peptide mRNA refines the management of patients with medullary thyroid cancer and may replace calcitonin-stimulation tests.

Cléber P Camacho, Susan C Lindsey, Maria Clara C Melo, Ji H Yang, Fausto Germano-Neto, Flávia de O F Valente, Thiago R N Lima, Rosa Paula M Biscolla, José G H Vieira, Janete M Cerutti and 2 more

Open access · greenAbstract read
In one paragraph

Article in Thyroid : official journal of the American Thyroid Association, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Calcitonin: current concepts and differential diagnosis.Therapeutic advances in endocrinology and metabolism · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Observational
  8. Article
  9. TheBioMed research international · 2017
    Article
  10. Article
  11. Article
  12. 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

12 authors at 1 institution in 1 country.

Cléber P CamachoLaboratory of Molecular and Translational Endocrinology, Department of Medicine, Escola Paulista de Medicina, Federal University of São Paulo, São Paulo, Brazil.
Susan C Lindsey
Maria Clara C Melo
Ji H Yang
Fausto Germano-Neto
Flávia de O F Valente
Thiago R N Lima
Rosa Paula M Biscolla
José G H Vieira
Janete M Cerutti
Magnus R Dias-da-Silva
Rui M B Maciel
Associação Paulista de Medicina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerum calcitonin (sCT) is the main tumor marker for medullary thyroid cancer (MTC), but it has certain limitations. Various sCT assays may have important intra-assay or interassay variation and may yield different and sometimes conflicting results. A pentagastrin- or calcium-stimulation calcitonin (CT) test may be desirable in some situations. Alternatively, or in the absence of the stimulation test, mRNA detection offers the advantages of being more comfortable and less invasive; it only requires blood collection and has no side effects. The objective of this study was to investigate the applicability of measuring calcitonin-related polypeptide alpha (CALCA) gene transcripts (CT-CALCA and calcitonin gene-related peptide [CGRP]-CALCA) in patients with MTC and in relatives diagnosed with a RET mutation and to test mRNA as an alternative diagnostic tool for the calcitonin-stimulation test.

methodsTwenty-three healthy controls and 26 individuals evaluated for MTC were selected, including patients with sporadic or hereditary MTC and RET mutation-carrying relatives. For molecular analysis, RNA was extracted from peripheral blood, followed by cDNA synthesis using 3.5 μg of total RNA. Quantitative real-time polymerase chain reaction (RT-qPCR) was performed with SYBR Green and 200 nM of each primer for the two specific mRNA targets (CT-CALCA or CGRP-CALCA) and normalized with the ribosomal protein S8 as the reference gene.

resultsWe detected CALCA transcripts in the blood samples and observed a positive correlation between them (r=0.946, p<0.0001). Both mRNAs also correlated with sCT (CT-CALCA, r=0.713, p<0.0001; CGRP-CALCA, r=0.714, p<0.0001). The relative expression of CT-CALCA and CGRP-CALCA presented higher clinical sensitivity (86.67 and 100, respectively), specificity (97.06 and 97.06), positive predictive value (92.86 and 93.75), and negative predictive value (94.29 and 100), than did sCT (73.33, 82.35, 64.71, and 87.50, respectively). In addition, the CALCA transcript measurement mirrored the response to the pentagastrin test.

conclusionWe demonstrate that the measurement of CALCA gene transcripts in the bloodstream is feasible and may refine the management of patients with MTC and RET mutation-carrying relatives. We propose considering the application of this diagnostic tool as an alternative to the calcitonin-stimulation test.

Indexed as

Gene Expression Regulation, NeoplasticBiomarkers, TumorCalcitoninCalcitonin Gene-Related PeptideCarcinoma, NeuroendocrineCase-Control StudiesDNA, ComplementaryFemaleGene Expression ProfilingHumansMaleMutationPentagastrinPredictive Value of TestsProtein PrecursorsProto-Oncogene Proteins c-retBiomarkers, TumorCALCA protein, humanCalcitoninCalcitonin Gene-Related PeptideDNA, ComplementaryPentagastrinProtein PrecursorsProto-Oncogene Proteins c-retRET protein, humanRNA, Messenger

Identifiers

PMID23259706
PMCPMC3593689
OpenAlexW2149408581

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.