Publications by authors named "Monia Zidane"

Background: Cardiac disease (CD) is a primary long-term diagnosed pathology among childhood cancer survivors. Dosiomics (radiomics extracted from the dose distribution) have received attention in the past few years to assess better the induced risk of radiotherapy (RT) than standard dosimetric features such as dose-volume indicators. Hence, using the spatial information contained in the dosiomics features with machine learning methods may improve the prediction of CD.

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Purpose: Childhood cancer survivors (CCS) have an increased risk of developing late chronic diseases, which can be influenced by the cancer type and its treatment. These chronic diseases can be severe and disabling, typically emerging years to decades after treatment. These deficits negatively impact quality of life, intelligence quotient, and memory.

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  • Second malignant neoplasm (SMN) poses a significant long-term risk for childhood cancer survivors and is influenced by genetic factors, alongside traditional treatments like chemotherapy and radiotherapy.
  • A systematic review analyzed eighteen studies exploring genetic components linked to SMN risk, encompassing various cancer types and focusing mainly on genes related to drug metabolism and DNA repair.
  • The variability in study designs and methods highlights the need for more standardized research, but the review offers a useful compilation of genetic variants associated with SMN risk, aiding future investigations.
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  • - The study investigates the genetic links between breast cancer (BC) and thyroid disorders, revealing a positive correlation between BC risk and thyroxine (FT4) levels, and a negative correlation with thyroid-stimulating hormone (TSH) levels, particularly in estrogen receptor-positive BC.
  • - Polygenic risk scores indicate that higher FT4 and hyperthyroidism risks are associated with increased BC risk, while higher TSH risk is linked to decreased BC risk, highlighting the role of genetics in these diseases.
  • - The research identifies 49 shared genetic loci connected to both BC and thyroid traits and suggests that certain brain and immune system-related genes play significant roles in the relationship between these conditions.
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  • - French Polynesia (FP) has a high incidence of differentiated thyroid cancer (DTC), and this study examined the genetic factors contributing to DTC risk in the native population, particularly due to past nuclear tests from 1966-1974.
  • - Researchers analyzed over 300,000 single nucleotide polymorphisms (SNPs) in 283 DTC cases and 418 controls, discovering genetic links associated with DTC at three specific regions on chromosomes 6, 10, and 17, indicating an increased risk.
  • - The findings suggest that these genetic loci could influence DTC risk, but the study recommends further investigation using whole genome sequencing to better understand these factors, as the current methods may not fully capture the
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Objective: The aim of this study was to identify risk factors for obesity in childhood cancer survivors (CCSs).

Methods: The study included 3199 patients of the French Childhood Cancer Survivor Study cohort, with 303 patients with obesity who had returned the self-questionnaire. Analyses were adjusted for social deprivation index and sex.

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Importance: Due to the amount of iodine 131 released in nuclear tests and its active uptake by the thyroid, differentiated thyroid carcinoma (DTC) is the most serious health risk for the population living near sites of nuclear tests. Whether low doses to the thyroid from nuclear fallout are associated with increased risk of thyroid cancer remains a controversial issue in medicine and public health, and a misunderstanding of this issue may be associated with overdiagnosis of DTCs.

Design, Setting, And Participants: This case-control study was conducted by extending a case-control study published in 2010 that included DTCs diagnosed between 1984 and 2003 by adding DTCs diagnosed between 2004 and 2016 and improving the dose assessment methodology.

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Background: Given the increased use and diversity of diagnostic procedures, it is important to understand genetic susceptibility to radiation-induced thyroid cancer.

Methods: On the basis of self-declared diagnostic radiology examination records in addition to existing literature, we estimated the radiation dose delivered to the thyroid gland from diagnostic procedures during childhood and adulthood in two case-control studies conducted in France. A total of 1,071 differentiated thyroid cancer (DTC) cases and 1,188 controls from the combined studies were genotyped using a custom-made Illumina OncoArray DNA chip.

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  • The first study linking ionizing radiation (IR) exposure to differentiated thyroid cancer (DTC) was published 70 years ago, suggesting that genetic variations in DNA repair mechanisms could influence how individuals react to IR damage.
  • A review of existing research found nine articles that identified ten genetic variants related to DTC risk from IR exposure, with some variants also linked to sporadic DTC.
  • There is a need for further research with larger groups and detailed radiation exposure data, especially since current studies lack information on children treated with radiotherapy.
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Background: In French Polynesia, thyroid cancer mortality and incidence is reported to be the highest in the world. Excessive levels of non-essential trace elements (nETE) in the body are associated with several types of cancer. Objective: The present study aims to provide quantitative information on food contamination by mercury (Hg), lead (Pb), arsenic (As) and cadmium (Cd) in French Polynesia and its potential correlation with measurements performed in fingernails of Polynesians, and then to investigate the potential association between these nETE and different thyroid cancer risks.

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