"/>

麻豆中文字幕丨欧美一级免费在线观看丨国产成人无码av在线播放无广告丨国产第一毛片丨国产视频观看丨七妺福利精品导航大全丨国产亚洲精品自在久久vr丨国产成人在线看丨国产超碰人人模人人爽人人喊丨欧美色图激情小说丨欧美中文字幕在线播放丨老少交欧美另类丨色香蕉在线丨美女大黄网站丨蜜臀av性久久久久蜜臀aⅴ麻豆丨欧美亚洲国产精品久久蜜芽直播丨久久99日韩国产精品久久99丨亚洲黄色免费看丨极品少妇xxx丨国产美女极度色诱视频www

FDA authorizes first direct-to-consumer test on breast cancer gene mutations

Source: Xinhua    2018-03-07 14:19:12

WASHINGTON, March 6 (Xinhua) -- The U.S. Food and Drug Administration (FDA) authorized on Tuesday the first direct-to-consumer (DTC) test which can report three mutations in the BRCA breast cancer genes while giving strong warnings of its possible improper application.

The test analyzes DNA from a self-collected saliva sample to describe if a woman is at increased risk of developing breast or ovarian cancer, and if a man is at increased risk of developing breast or prostate cancer, according to the FDA.

"BRCA" stands for "Breast Cancer gene." BRCA1 and BRCA2 are two different genes that have been found to impact a person's chances of developing breast cancer.

"This test provides information to certain individuals who may be at increased breast, ovarian or prostate cancer risk and who might not otherwise get genetic screening, and is a step forward in the availability of DTC genetic tests," said Donald St. Pierre, acting director of the Office of In Vitro Diagnostics and Radiological Health at the FDA's Center for Devices and Radiological Health.

However, Pierre said "it has a lot of caveats" because only a small percentage of Americans carry one of these three mutations, and most BRCA mutations that increase an individual's risk are not detected by this test.

"The test should not be used as a substitute for seeing your doctor for cancer screenings or counseling on genetic and lifestyle factors that can increase or decrease cancer risk," Pierre said.

The test detects three out of more than 1,000 known BRCA mutations. This means a negative result does not rule out the possibility that an individual carries other BRCA mutations that increase cancer risk, according to the FDA.

About one in 400 people carries mutated BRCA1 or BRCA2 genes. Also, the FDA warned that most cases of cancer are not caused by hereditary gene mutations but caused by smoking, obesity, hormone use and other lifestyle factors.

The FDA granted the marketing authorization to 23andMe, a DNA genetic testing and analysis company based in Silicon Valley.

Editor: Jiaxin
Related News
Xinhuanet

FDA authorizes first direct-to-consumer test on breast cancer gene mutations

Source: Xinhua 2018-03-07 14:19:12

WASHINGTON, March 6 (Xinhua) -- The U.S. Food and Drug Administration (FDA) authorized on Tuesday the first direct-to-consumer (DTC) test which can report three mutations in the BRCA breast cancer genes while giving strong warnings of its possible improper application.

The test analyzes DNA from a self-collected saliva sample to describe if a woman is at increased risk of developing breast or ovarian cancer, and if a man is at increased risk of developing breast or prostate cancer, according to the FDA.

"BRCA" stands for "Breast Cancer gene." BRCA1 and BRCA2 are two different genes that have been found to impact a person's chances of developing breast cancer.

"This test provides information to certain individuals who may be at increased breast, ovarian or prostate cancer risk and who might not otherwise get genetic screening, and is a step forward in the availability of DTC genetic tests," said Donald St. Pierre, acting director of the Office of In Vitro Diagnostics and Radiological Health at the FDA's Center for Devices and Radiological Health.

However, Pierre said "it has a lot of caveats" because only a small percentage of Americans carry one of these three mutations, and most BRCA mutations that increase an individual's risk are not detected by this test.

"The test should not be used as a substitute for seeing your doctor for cancer screenings or counseling on genetic and lifestyle factors that can increase or decrease cancer risk," Pierre said.

The test detects three out of more than 1,000 known BRCA mutations. This means a negative result does not rule out the possibility that an individual carries other BRCA mutations that increase cancer risk, according to the FDA.

About one in 400 people carries mutated BRCA1 or BRCA2 genes. Also, the FDA warned that most cases of cancer are not caused by hereditary gene mutations but caused by smoking, obesity, hormone use and other lifestyle factors.

The FDA granted the marketing authorization to 23andMe, a DNA genetic testing and analysis company based in Silicon Valley.

[Editor: huaxia]
010020070750000000000000011100001370220631