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studi menunjukkan , Gangguan bipolar memiliki link genetik untuk autisme----T-REC semarang--komunitas reptil-semarang--KSE-komunitas satwa eksotik--berita artikel terkait tentang autis dan autisme dan gangguan kejiwaan

studi menunjukkan , Gangguan bipolar memiliki link genetik untuk autisme
Temuan dari dua pendekatan menambah bukti kerentanan genetik dibagi di gangguan kejiwaan utama

Date:
May 4, 2016
Source:
University of Iowa Health Care
Summary:
penelitian baru menunjukkan , Mungkin ada tumpang tindih antara variasi genetik langka terkait dengan gangguan bipolar dan mereka yang terlibat dalam skizofrenia dan autisme
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Sebuah studi baru menunjukkan mungkin ada tumpang tindih antara variasi genetik langka terkait dengan gangguan bipolar / bipolar disorder  (BD) dan mereka yang terlibat dalam skizofrenia dan autisme.
Penelitian ini dilakukan oleh para peneliti di University of Iowa Carver College of Medicine, Johns Hopkins School of Medicine, dan Cold Spring Harbor Laboratory dan diterbitkan baru-baru dalam JAMA Psychiatry, menambah pemahaman yang berkembang bahwa banyak penyakit kejiwaan berbagi akar genetik, tapi merupakan salah satu yang  pertama menyarankan tumpang tindih genetik antara gangguan bipolar dan autisme.

Gangguan bipolar adalah salah satu penyakit jiwa yang paling penting karena cukup umum - yang mempengaruhi antara 1 dan 3 persen dari populasi - dan cukup melemahkan. Meskipun banyak pasien dibantu oleh perawatan, seperti lithium, sekitar sepertiga dari orang yang terkena BD tidak melakukannya dengan baik dengan terapi saat ini. Meskipun itu lama diketahui bahwa gangguan bipolar sangat diwariskan, mengidentifikasi varian genetik tertentu yang berkontribusi terhadap penyakit telah terbukti sulit.
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Bipolar disorder has genetic links to autism, study shows
Findings from a two-pronged approach add to evidence of shared genetic susceptibility across major psychiatric disorders
Date:
May 4, 2016
Source:
University of Iowa Health Care
Summary:
There may be an overlap between rare genetic variations linked to bipolar disorder and those implicated in schizophrenia and autism, new research suggests.
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A new study suggests there may be an overlap between rare genetic variations linked to bipolar disorder (BD) and those implicated in schizophrenia and autism.
The study, by researchers at the University of Iowa Carver College of Medicine, Johns Hopkins School of Medicine, and Cold Spring Harbor Laboratory and published recently in JAMA Psychiatry, adds to the growing understanding that many psychiatric diseases share genetic roots, but is among the first to suggest a genetic overlap between bipolar disorder and autism.
Bipolar disorder is one of the most important psychiatric illnesses because it is fairly common -- affecting between 1 and 3 percent of the population -- and quite debilitating. Although many patients are helped by treatments, such as lithium, about one third of people affected by BD do not do well with current therapies. Although it's long been known that bipolar disorder is highly heritable, identifying specific genetic variants that contribute to the illness has proven difficult.
Within the last decade, advances in human genome studies have helped uncover several so-called common variations, but none of these variations alone have a large effect. Even more recently, the advent of rapid and relatively cheap next-generation gene sequencing technology has provided an opportunity to find rare variations that might individually have a large effect.
"Common variations are thought to each individually have only a tiny impact -- for example, increasing a person's likelihood of getting a disease by 10 to 20 percent," says James Potash, MD, UI professor and DEO of psychiatry, and senior author of the new study. "The hope with rare variations is that they individually have a much bigger impact, like doubling or quadrupling risk for disease."
Potash and his colleagues devised a two-pronged strategy, combining a case-control approach with family-based exome sequencing to maximize their chances of identifying rare variants that contribute to BD.
The idea behind the case-control approach is simple: if a genetic variant is found more often in the group of individuals who have the disease compared to a control group of people without the condition, then the gene variation might be associated with increasing susceptibility to the disease. Very large datasets are key to the success of this approach.

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Ide di balik pendekatan kasus kontrol sederhana : jika varian genetik ditemukan lebih sering pada kelompok individu yang memiliki penyakit dibandingkan dengan kelompok kontrol dari orang tanpa kondisi , maka variasi gen mungkin terkait dengan peningkatan kerentanan terhadap penyakit.dataset sangat besar adalah kunci untuk keberhasilan pendekatan ini .
Exome sequencing of families affected by a disease is more sophisticated. Comparing exome sequences of related individuals, affected and unaffected by BD, can distinguish variants that "travel with" or segregate with the disease. This approach has long been used to identify gene variants or mutations that are passed from parents to children that cause disease.
Overall the family study identified 84 rare variants (in 82 genes) that segregated with BD and that were also predicted to be damaging to the proteins encoded by those genes. The team then tested the likelihood that these rare variations might be involved in causing BD by looking for them in three large case-control datasets that included genome sequences from a total of 3,541 individuals with BD and 4,774 control patients.
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Secara keseluruhan studi keluarga diidentifikasi 84 varian langka ( di 82 gen ) yang dipisahkan dengan BD dan yang juga diprediksi akan merusak protein yang dikodekan oleh gen mereka . Tim kemudian menguji kemungkinan bahwa variasi langka mungkin terlibat dalam menyebabkan BD dengan mencari mereka di tiga dataset kasus - kontrol besar yang termasuk urutan genom dari total 3.541 individu dengan BD dan 4.774 pasien kontrol .

Despite the relatively large size of the combined datasets, the approach was not powerful enough to identify any of the individual rare variants as definitively associated with BD. However, 19 genes stood out as being over-represented in BD cases compared to controls.
"The results were not strong enough for us to say 'we have pinpointed the genetic culprits.' But it was strong enough for us to remain interested in these genes as potential contributors to bipolar disorder," says Potash, who also is the Paul W. Penningroth Professor and Chair of Psychiatry and a member of the Pappajohn Biomedical Institute at the UI.
However, when the team considered the 19 genes as a group, they realized that several were also members of groups of genes that had been implicated in autism and schizophrenia.
"It turned out that the schizophrenia and the autism genes were all more represented among our 82 genes than you would expect by chance," Potash says. "And when we looked at our whittled down group of 19 genes, the autism genes continued to be unexpectedly prominent among them.
"With studies like this we are finally, after decades of effort, making real progress in nailing down groups of genes and variations in them that play a role in causing bipolar disorder," Potash adds. "The mechanistic insights we gain from identifying associated genes we hope will point us in the direction of developing new treatments to make a difference for the many people affected by this illness.

Story Source:
The above post is reprinted from materials provided byUniversity of Iowa Health CareNote: Materials may be edited for content and length.

Journal Reference:
1.      Fernando S. Goes, Mehdi Pirooznia, Jennifer S. Parla, Melissa Kramer, Elena Ghiban, Senem Mavruk, Yun-Ching Chen, Eric T. Monson, Virginia L. Willour, Rachel Karchin, Matthew Flickinger, Adam E. Locke, Shawn E. Levy, Laura J. Scott, Michael Boehnke, Eli Stahl, Jennifer L. Moran, Christina M. Hultman, Mikael Landén, Shaun M. Purcell, Pamela Sklar, Peter P. Zandi, W. Richard McCombie, James B. Potash. Exome Sequencing of Familial Bipolar DisorderJAMA Psychiatry, 2016; DOI:10.1001/jamapsychiatry.2016.0251

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