Evidence map›Paper›PMID 26739382›Full record

ArticleJournal of neurology2016

Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors.

Maria Laura Ester Bianchi, Emanuele Leoncini, Marcella Masciullo, Anna Modoni, Shahinaz M Gadalla, Roberto Massa, Emanuele Rastelli, Chiara Terracciano, Giovanni Antonini, Elisabetta Bucci and 5 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Journal of neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Cancer and Myotonic Dystrophy.Journal of clinical medicine · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Benign tumors in myotonic dystrophy type I target disease-related cancer sites.Annals of clinical and translational neurology · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Imaging of the thymus in myotonic dystrophy type 1.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2018
    Article
  17. Article
  18. Article
  19. Myotonic Dystrophy Type 1 Management and Therapeutics.Current treatment options in neurology · 2016
    Review
  20. An Unusual Case of Hybrid Odontogenic Tumor in Type 1 Myotonic Dystrophy Patient.International journal of applied & basic medical research
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 2 countries.

Maria Laura Ester BianchiDepartment of Geriatrics, Neuroscience and Orthopedics, Università Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy.
Emanuele LeonciniInstitute of Public Health, Section of Hygiene, UCSC, Rome, Italy.
Marcella MasciulloIRCSS Fondazione Santa Lucia, Rome, Italy.
Anna ModoniDepartment of Geriatrics, Neuroscience and Orthopedics, Università Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy.
Shahinaz M GadallaClinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
Roberto MassaDepartment of Systems Medicine (Neurology), University of Rome Tor Vergata, Rome, Italy.
Emanuele RastelliDepartment of Systems Medicine (Neurology), University of Rome Tor Vergata, Rome, Italy.
Chiara TerraccianoDepartment of Systems Medicine (Neurology), University of Rome Tor Vergata, Rome, Italy.
Giovanni AntoniniDepartment of Neurosciences, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Rome, Italy.
Elisabetta BucciDepartment of Neurosciences, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Rome, Italy.
Antonio PetrucciUnità Operativa Complessa Neurologia e Neurofisiopatologia, Azienda Ospedaliera San Camillo Forlanini, Rome, Italy.
Sandro CostanziUnit of Medical Genetics, Center for Neuromuscular and Neurological Rare Diseases, S. Camillo Forlanini Hospital, Rome, Italy.
Massimo SantoroFondazione Don Carlo Gnocchi Onlus, Milan, Italy.
Stefania BocciaInstitute of Public Health, Section of Hygiene, UCSC, Rome, Italy.
Gabriella SilvestriDepartment of Geriatrics, Neuroscience and Orthopedics, Università Cattolica del Sacro Cuore, Largo F. Vito 1, 00168, Rome, Italy. gsilvestri@rm.unicatt.it.
Università Cattolica del Sacro Cuore · ITUniversity of Rome Tor Vergata · ITSapienza University of Rome · ITAzienda Ospedaliera San Camillo-Forlanini · ITCarlo Forlanini Hospital · ITDivision of Cancer Epidemiology and GeneticsDon Carlo Gnocchi Foundation · ITFondazione Santa Lucia · IT

Funding

Clinical Genetic Studies of Familial and Hereditary Cancer SyndromesZIACP010144 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SAVAGE, SHARON A. · 2009 to 2025
$111.8M
Intramural NIH HHS ZIA CP010144
6 · The paper itself

Abstract

Recent studies documented an increased risk of neoplasm in patients with myotonic dystrophies (DM). Yet, none of these studies evaluated the contribution of common cancer risk factors in such observation. In this study, we included a cohort of patients (n = 255) with an established molecular diagnosis of DM type 1 (DM1), and who receives their treatment in one of the four centers with recognized expertise in neuromuscular disorders in Rome. We estimated the prevalence of benign and malignant tumors, and assessed if lifestyle factors and/or specific disease features would be associated to their occurrence. Overall, 59 benign tumors in 54 patients and 19 malignant tumors in 17 patients were diagnosed. The most common malignant neoplasms were cancers of the skin (31.6%), thyroid (21.0%), ovary (10.5%), and breast (10.5%). Uterine fibroid was the most common benign tumor (37.6%) in women, while pilomatricoma was the most common in men (28.6%). Age at enrollment (OR = 1.02, 95% CI 1.00-1.05), and female gender (OR = 5.71, 95% CI 2.90-11.22) were associated with tumor development in DM1 patients, while thyroid disorders was associated with malignant tumors only in women (OR = 5.12, 95% CI 1.35-19.37). There was no association between tumor development and evaluated lifestyle factors. In conclusion, the lack of association between common cancer risk factors and tumor development in DM1 support a pathogenic link between tumors and DM1 itself, emphasizing the need for a systematic surveillance. Our observation of an association between thyroid diseases in women and cancer development needs confirmation.

Indexed as

Life StyleAdolescentAdultAge DistributionCohort StudiesFemaleHumansMaleMiddle AgedMyotonic DystrophyNeoplasmsRisk FactorsStatistics, NonparametricYoung AdultCancerMyotonic dystrophy type 1Risk factorsThyroid diseaseTumor

Identifiers

PMID26739382
PMCPMC7814867
OpenAlexW2229491895

What OpenQuestion holds

Textmetadata
LicenceTDM
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.