Science Current Events | Science News | Brightsurf.com
 
Email a Friend Send to a friend
Printer Friendly Print Should parents share the results of BRCA1/2 genetic testing with their children?

Should parents share the results of BRCA1/2 genetic testing with their children?

May 15, 2009

If you learned that you were at high risk of cancer because you carry the hereditary BRCA1/2 gene mutation, would you tell your children? A recent study at Fox Chase Cancer Center not only considered that question, but also took it to the next level and studied the parent perceptions of the impact of such a decision on children. The study will be presented at the 2009 Annual Meeting of the American Society of Clinical Oncology. BRCA1/2 are hereditary gene mutations that indicate an increased risk of developing breast cancer.

"We know that many people who carry the BRCA1/2 gene mutation share their genetic test results with their children," explained Angela Bradbury, MD, medical oncologist at Fox Chase and lead author on the study. "What we did not know was the impact this communication has on their children."




In order to learn the impact this has on children, researchers evaluated results from 163 parents who had BRCA1/2 testing. Of those, 52 tested positive for BRCA1/2. Just over 100 parents (66 percent) shared their results with at least one of their children, which totaled 323 children who were between the ages of 5 - 25. The child's age and parent cancer history had a direct correlation to whether or not they shared the results. Not surprising, those without a BRCA1/2 mutation were more likely to communicate test results than parents with a mutation.

Among parents who disclosed their results, few reported negative reactions from their children (9 percent) or that their child did not understand the information (11 percent). Overall, most parents reported that their children handled the information well, although negative reactions were more frequent among certain subgroups (younger children and those of parents with a mutation or a variant of uncertain significance).

"Many parents share genetic test results with their children," said Bradbury. "According to our research, most parents do not perceive their children to have adverse reactions to this information, although children who learn their parent tested positive for the

BRCA1/2 mutation or a variant of uncertain significance may be more susceptible to initial negative reactions. We certainly need to learn more about how children respond to this information."

Further research with parents and children will be done to explore psychosocial and behavioral responses to learning of hereditary risk during childhood and adolescence, and to inform the development of interventions to optimize adaptive responses to early communication of genetic risk.

Fox Chase Cancer Center



Related Gene Mutation Current Events and Gene Mutation News Articles Gene Mutation Current Events and Gene Mutation News RSS Gene Mutation Current Events and Gene Mutation News RSS
Maize cell wall genes identified, giving boost to biofuel research
Purdue University scientists have helped identify and group the genes thought to be responsible for cell wall development in maize, an effort that expands their ability to discover ways to produce the biomass best suited for biofuels production.

Stanford scientist's new findings of autism-associated synapse alterations lead to coveted NIH grant
A Stanford University School of Medicine researcher has pinpointed the mechanism by which a gene associated with both autism and schizophrenia influences behavior in mice. And just recently, he received a $1.65 million government grant to expand his efforts to include many more such genes.

Gene mingling increases sudden death risk
A multi-national research team has discovered that two genetic factors converge to increase the risk of sudden cardiac death.

Breast cancer patients with high risk gene diagnosed 6 years earlier than generation before
Women with a deleterious gene mutation are diagnosed with breast cancer six years earlier than relatives of the previous generation who also had the disease and/or ovarian cancer, according to new research from The University of Texas M. D. Anderson Cancer Center.

New Approach for the Treatment of Malignant Brain Tumors
Initial chemotherapy alone after surgery is just as successful as initial radiation therapy for patients from whom a very malignant brain tumor (anaplastic glioma) was removed. With this treatment, the patients survive on average > 30 months without a recurrence.

Genetic discovery could break wine industry bottleneck, accelerate grapevine breeding
One of the best known episodes in the 8000-year history of grapevine cultivation led to biological changes that have not been well understood - until now.

Racial Disparities in Diabetes Prevalence Linked to Living Conditions
The higher incidence of diabetes among African Americans when compared to whites may have more to do with living conditions than genetics, according to a study led by researchers at the Johns Hopkins Bloomberg School of Public Health.

Team reveals molecular mechanism underlying a form of diabetes
By investigating a rare and severe form of diabetes in children, University of Iowa researchers have discovered a new molecular mechanism that regulates specialized pancreatic cells and insulin secretion.

New research strategy for understanding drug resistance in leukemia
UCSF researchers have developed a new approach to identify specific genes that influence how cancer cells respond to drugs and how they become resistant. This strategy, which involves producing diverse genetic mutations that result in leukemia and associating specific mutations with treatment outcomes, will enable researchers to better understand how drug resistance occurs in leukemia and other cancers, and has important long-term implications for the development of more effective therapies.

Not only the gene itself, its abnormal regulation can also trigger short stature
A specific gene is particularly frequently involved in the development of short stature. Researchers in Heidelberg have now discovered that sequences of genetic material on the X and Y chromosome that regulate this gene are also crucial for growth in children.
More Gene Mutation Current Events and Gene Mutation News Articles
Gene: Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, ... Gene- centered view of evolution

Gene: Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, ... Gene- centered view of evolution
by Frederic P. Miller (Editor), Agnes F. Vandome (Editor), John McBrewster (Editor)

Gene. History of genetics, Mendelian inheritance, Gene expression, Genetic code, Mutation, Gene targeting, The Selfish Gene, Copy number variation, DNA, Epigenetics, Gene- centered view of evolution, Gene therapy, Genetic algorithm, Genetics, Genome, Genomics, List of human genes, Meme, Pseudogene, Predictive medicine

ABC News Nightline Confronting a Genetic Legacy

ABC News Nightline Confronting a Genetic Legacy

Imagine you were told that you carry a gene that makes it all but certain you will one day get breast cancer, ovarian cancer or both. What would you do? Jessica Queller, a 35-year-old writer for the hit series "Gilmore Girls," has had to answer that question. In 2004, she found out that she carries the BRCA1 gene mutation, or, the breast cancer gene. According to one study, possessing that gene means she has an 85 percent chance of developing breast cancer before the age of 70 and a 50 percent chance of developing it before the age of 50. Queller took the test because her mother had recently died of ovarian cancer, and several years earlier had fought and beaten breast cancer. Queller now knows what her mother never did, and now she is left in a place where modern science has told her...

  MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or mammography.(Women's ... An article from: Family Practice News
by Betsy Bates (Author)

This digital document is an article from Family Practice News, published by International Medical News Group on December 1, 2004. The length of the article is 979 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: MRI best for carriers of BRCA gene mutations: study shows MRI detects more breast cancers in this population than do ultrasound or mammography.(Women's Health)(Magnetic resonance imaging)
Author: Betsy Bates
Publication: Family Practice News (Magazine/Journal)
Date: December 1, 2004
Publisher: International Medical News Group
Volume: 34 Issue: 23 Page:...

  Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric ... An article from: Clinical Psychiatry News
by Christine Kilgore (Author)

This digital document is an article from Clinical Psychiatry News, published by International Medical News Group on April 1, 2005. The length of the article is 933 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: Mutation linked to some cases of Parkinson's: identifying gene raises ethical questions about its use in testing, given the lack of preventive therapy.(Neuropsychiatric Medicine)
Author: Christine Kilgore
Publication: Clinical Psychiatry News (Magazine/Journal)
Date: April 1, 2005
Publisher: International Medical News Group
Volume: 33 Issue: 4 Page:...

  Limited Family Structure and BRCA Gene Mutation Status in Single Cases of Breast Cancer / Identifying Widely Covered Drugs and Drug Coverage Variation Among Medicare Part D Formularies (JAMA: The Journal of the American Medical Association, Volume 297, Number 23, June 20, 2007)
by J. N. Weitzel (Author)



Mouse lymphoma thymidine kinase gene mutation assay: Meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations ... Toxicology and Environmental Mutagenesis]

Mouse lymphoma thymidine kinase gene mutation assay: Meeting of the International Workshop on Genotoxicity Testing, San Francisco, 2005, recommendations ... Toxicology and Environmental Mutagenesis]
by M.M. Moore (Author), M. Honma (Author), J. Clements (Author), G. Bolcsfoldi (Author)

This digital document is a journal article from Mut.Res.-Genetic Toxicology and Environmental Mutagenesis, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
The Mouse Lymphoma Assay (MLA) Workgroup of the International Workshop on Genotoxicity Testing (IWGT), comprised of experts from Japan, Europe and the United States, met on September 9, 2005, in San Francisco, CA, USA. This meeting of the MLA Workgroup was devoted to reaching a consensus on issues involved with 24-h treatment. Recommendations were made concerning the acceptable values for the negative/solvent control (mutant frequency, cloning efficiency and suspension growth)...

American Cancer Society Film: Time is Life (1949) [DVD]

American Cancer Society Film: Time is Life (1949) [DVD]

Time is Life highlights the importance of time in combating the second highest cause of death in the world, cancer. The film also underscores the efforts of the American Cancer Society towards the alleviation, if not elimination, of cancer in the American society. The film starts with Mary Bronson being stressed out with the possibility of having a cancer. Cancer is not given proper attention by the public so it causes insurmountable effects on people in the society. Cancer chooses no one. In addition, the film gives conveying figures on cancer fatalities in the United States saying that one in every eight American has cancer. The film has also mentioned that cancer has killed more Americans than the slaughter at the Pearl Harbor and Tokyo Bay during World War Two. The film also dispels...

  Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.: An article from: Human Biology
by C.A. Oliveira (Author), F. Alexandrino (Author), K. Abe-Sandes (Author), W.A. Silva (Author), A.T. Maciel-Guerra (Author), L.A. Magna (Author), E.L. Sartorato (Author)

This digital document is an article from Human Biology, published by Wayne State University Press on April 1, 2004. The length of the article is 1423 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: KEY WORDS: GJB2, BRAZILIAN POPULATION, CONGENITAL DEAFNESS

Citation Details
Title: Frequency of the 35delG mutation in the GJB2 gene in samples of European, Asian, and African Brazilians.
Author: C.A. Oliveira
Publication: Human Biology (Refereed)
Date: April 1, 2004
Publisher: Wayne State University Press
Volume: 76 Issue: 2 Page: 313(4)

Distributed by...

  Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.: An article from: Human Biology
by Erardo Merino-Ibarra (Author), Sergio Castillo (Author), Pilar Mozas (Author), Ana Cenarro (Author), Esperanza Martorell (Author), Jose Luis Diaz (Author), Manuel Suarez-Tembra (Author), Rodrigo Alonso (Author), Fernando Civeira (Author), Pedro Mata (Author), Miguel Pocovi (Author)

This digital document is an article from Human Biology, published by Thomson Gale on October 1, 2005. The length of the article is 4221 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: KEY WORDS: FAMILIAL DEFECTIVE APOB, AUTOSOMAL DOMINANT MONOGENIC HYPERCHOLESTEROLEMIA (ADMH), HYPERCHOLESTEROLEMIA, APOB, LDLR, R3500Q MUTATION, T3552T MUTATION, SSCP (SINGLE-STRAND CONFORMATION POLYMORPHISM) ANALYSIS, SPAIN.

Citation Details
Title: Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.
Author: Erardo...

  657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract): An article from: Human Biology
by Mustafa Tekin (Author), Duygu Akcayoz (Author), Canan Ucar (Author), Huseyin Gulen (Author), Nejat Akar (Author)

This digital document is an article from Human Biology, published by Thomson Gale on June 1, 2005. The length of the article is 1366 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

From the author: KEY WORDS: FOUNDER EFFECT, NIJMEGEN BREAKAGE SYNDROME, NBS1, SLAVS, TURKS.

Citation Details
Title: 657del5 mutation of the Nijmegen breakage syndrome gene (NBS1) in the Turkish population.(Author Abstract)
Author: Mustafa Tekin
Publication: Human Biology (Magazine/Journal)
Date: June 1, 2005
Publisher: Thomson Gale
Volume: 77 Issue: 3 Page: 393(5)

Article Type: Author...

© 2009 BrightSurf.com