Schizophrenia Ties to Random DNA Mutations Bolstered in Study

Spontaneous defects in DNA may trigger schizophrenia, according to research that bolsters results of smaller studies aimed at finding the genetic causes of the disabling mental disorder.

In the largest study of its kind, international research teams found evidence that schizophrenia can be caused when genes are duplicated or deleted in an often random process that isn't inherited from parents, according to reports published today in the journals Nature and Nature Genetics. Scientists found that people with schizophrenia are more than 10 times as likely to have these rare chromosomal alterations as people who don't have the illness.

While the findings fill in parts of the puzzle of the disease, they also suggest it may be caused by a complex set of genetic flaws, which could complicate the search for effective treatments.

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Searching for Similar Diagnosis Through DNA

The girls had never met, but they looked like sisters.

There was no missing the similarities: the flat bridge of their noses, the thin lips, the fold near the corner of their eyes. And to the families of 14-year-old Samantha Napier and 4-year-old Taygen Lane there was something else, too. In the likeness was lurking an explanation for the learning difficulties, the digestion problems, the head-banging that had troubled each of them, for so long.

Several of the adults wiped tears from their eyes. “It’s like meeting family,” said Jessica Houk, Samantha’s older sister, who accompanied her and their mother to a Kentucky amusement park last July to greet Taygen.

But the two families are not related, and would never have met save for an unusual bond: a few months earlier, a newly available DNA test revealed that Samantha and Taygen share an identical nick in the short arm of their 16th chromosomes.

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