Early detection of prostate cancer can be aided by knowledge of the role that family history plays in the disease’s risk.
Family History and Genetic Predisposition
Having a family history of prostate cancer can double your risk of developing the disease. The closer the relative and the earlier their diagnosis, the more your risk may increase.
This heightened risk is due to inherited gene mutations that may be passed down from generation to generation. These genetic mutations, such as changes in the BRCA1 or BRCA2 genes can also raise the likelihood of prostate cancer in men.
Other Genetic Syndromes
In addition to the BRCA genes, Lynch syndrome is another inherited condition that can elevate the risk of prostate cancer. Men with Lynch syndrome have a higher chance of developing several types of cancer, including prostate, colon, and endometrial cancer. If there is a history of these cancers in your family, it is important to share this information with your doctor.
Screening and Early Detection
If you have a family history of prostate cancer, regular screenings can play a vital role in early detection and successful treatment. The most common screening methods include the prostate-specific antigen (PSA) blood test and a digital rectal exam (DRE).
For men with a family history of prostate cancer, screening may begin earlier. It can be around the age of 40 or 45 compared to men with no family history, who usually start screening at 50.
Book Your Prostate Cancer Treatment in Hartford, Enfield & Glastonbury, CT
A family history of prostate cancer can increase the risk of developing the disease. However, regular screenings and awareness of genetic factors can help detect them early.
If prostate cancer runs in your family, don’t hesitate to call us at 860-522-2251 and schedule an appointment with Greater Hartford Urology Group.
