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Study shows higher cancer risk among twins, siblings

In fraternal twins it amounted to a 37 per cent risk of developing cancer if a co-twin was diagnosed.

Miami: Twins share the same genes, and when one gets cancer, the other faces a higher risk of getting sick too, according to a study today that included 200,000 people.

But just because one twin falls ill does not mean that the other is certain to get the same cancer, or any cancer at all, according the report in the Journal of the American Medical Association (JAMA).

In fact, the amount of increased risk of cancer was just 14 per cent higher in identical pairs in which one twin was diagnosed with cancer.

Identical twins develop from the same egg and share the exact same genetic material.

Among fraternal twins, which develop from two eggs and are as genetically similar as typical biological siblings, the risk of cancer in a twin whose co-twin was infected was five percent higher.

The twins in the study hailed from Denmark, Finland, Sweden and Norway -- all countries that maintain detailed health registries -- and were followed between 1943 and 2010.

When researchers looked at the group as a whole, they found that about one in three individuals developed cancer (32 per cent).

Therefore, the risk of cancer in an identical twin whose twin was diagnosed was calculated to be 46 per cent.

In fraternal twins it amounted to a 37 per cent risk of developing cancer if a co-twin was diagnosed.

The exact same cancer was diagnosed in 38 per cent of identical twins and 26 percent of fraternal pairs.

The cancers that were most likely to be shared among twins were skin melanoma (58 per cent), prostate (57 per cent), non melanoma skin (43 per cent), ovary (39 per cent), kidney (38 per cent), breast (31 per cent), uterine cancer (27 per cent).

"Because of this study's size and long follow-up, we can now see key genetic effects for many cancers," said Jacob Hjelmborg, from the University of Southern Denmark and co-lead author of the study.

Researchers said the findings may help patients and doctors understand more about the hereditary risks of cancer, a disease that kills eight million people around the world each year.  

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