Spontaneous Mutations = in Schizophrenia are they due to Older Paternal Age

Science News Share Blog Mutations Responsible For 10 Percent Of Schizophrenia Pinpointed
ScienceDaily (May 30, 2008) — People with schizophrenia from families with no history of the illness were found to harbor eight times more spontaneous mutations -- most in pathways affecting brain development -- than healthy controls. By contrast, no spontaneous mutations were found in people with schizophrenia who had family histories of the illness. The findings strongly suggest that rare, spontaneous mutations likely contribute to vulnerability in cases of schizophrenia from previously unaffected families.



Scans of the genome of patients with schizophrenia have revealed rare spontaneous copy number mutations that account for at least 10 percent of the non-familial cases of the disease. Researchers describe specific genetic mutations present in individuals who have schizophrenia, but not present in their biological parents who do not have the disease.

This new data will help researchers account for the persistence of schizophrenia in the population despite low birth rates among people with the disease.

Researchers at Columbia University Medical Center scanned the genome of 1,077 people which included 152 individuals with schizophrenia, 159 individuals without schizophrenia, and both of their biological parents for copy number mutations. They found mutations, either a gain or loss of genes, in 15 individuals diagnosed with schizophrenia that were not present in the chromosomes of either biological unaffected parent. Only two of such mutations were found in those without schizophrenia. Study subjects were from the European-origin Afrikaner population in South Africa, a genetically homogenous population that is ideal for genetic evaluation.

"We now know the cause of around 10 percent of the cases of sporadic schizophrenia," said Maria Karayiorgou, M.D., professor of psychiatry, Columbia University Medical Center, the senior author on the study. "Schizophrenia is not as much of a 'big black box' as it used to be. The identification of these genes lets us know what brain development pathways are involved in disease onset, so that in the future we can look at better ways of treating this devastating disease."

Schizophrenia affects approximately 1 percent of the population worldwide. About 40 percent of the disease is thought to be inherited, with the other 60 percent sporadically showing up in people whose family history does not include the disease.

One of the new or de novo mutations researchers found in more than one affected individual in this study was a deletion of a region of chromosome 22. Dr. Karayiorgou had previously provided evidence that loss of genes in this region, 22q11.2, was responsible for introducing "new" or sporadic cases of schizophrenia in the population. This confirms 22q11.2 as the only known recurrent such mutation linked to schizophrenia.

"We have already demonstrated 22q11.2 to be involved in sporadic schizophrenia and we have made considerable progress in understanding the underlying biological mechanisms," said Dr. Gogos. "Now, we have a new set of mutations that we can investigate. The more information we have about the biological basis for this disease, the more information we can provide to those who suffer from it and their families."

"Such abnormal deletions or duplications of genetic material are increasingly being implicated in schizophrenia and autism," explains National Institute of Mental Health Director Thomas R. Insel, M.D. "Now we have a dramatic demonstration that genetic vulnerabilities for these illnesses may stem from both hereditary and non-hereditary processes. This line of research holds promise for improved treatments -- and perhaps someday even prevention -- of developmental brain disorders."

Karayiorgou and co-senior author Joseph A. Gogos, M.D., Ph.D., associate professor of physiology and neuroscience at Columbia University Medical Center, agree that the goal is for psychiatrists to be able to inform patients that they have a mutation that is causing their disease and ultimately to be able to tailor treatments to individual patients based on their specific mutation. This tailored treatment is a ways off, according to Dr. Karayiorgou, but she says patients and their families are relieved to know that there is a biological cause of their illness.

The researchers plan to extend their screen for additional de novo mutations by using increased resolution scans to study additional families. They also plan to scrutinize further genes affected by the identified mutations through human genetics and animal model approaches.

This study was supported by the National Institutes of Health's (NIH) National Institute of Mental Health (NIMH) and the Lieber Center for Schizophrenia Research at Columbia University Medical Center.


--------------------------------------------------------------------------------

Journal reference:

Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M.. Strong association of de novo copy number mutations with sporadic schizophrenia.. Nature Genetics, May 30, 2008
Adapted from materials provided by Columbia University Medical Center.
Need to cite this story in your essay, paper, or report? Use one of the following formats:
APA

MLA Columbia University Medical Center (2008, May 30). Gene Mutations Responsible For 10 Percent Of Schizophrenia Pinpointed. ScienceDaily. Retrieved May 30, 2008, from http://www.sciencedaily.com­ /releases/2008/05/080530132220.htmenlarge

A. Genetic mutations that result in fewer than two (middle offspring) or more than two (right offspring) genomic copies of a chromosomal region, are present in individuals who have schizophrenia, but not present in their biological parents who do not have the disease. For comparison, a family with an unaffected offspring is indicated at the left. B. A schematic representation of a spontaneous copy number mutation found in one individual with schizophrenia. This mutation results in loss of genes, including a gene affecting neurodevelopment (EPHB1). (Credit: P. Alexander Arguello, Copyright Columbia University Medical Center, May 2008)
Ads by GoogleAdvertise here
--------------------------------------------------------------------------------