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<h2 class="element-invisible">You are here</h2><div class="breadcrumb"><a href="/">Home</a> » <a href="/news-events">News & Events</a> » <a href="/news-events/nih-research-matters">NIH Research Matters</a></div> <div class="l-region l-region--section-header">
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<p class="publishdate"><span property="dc:date" datatype="xsd:dateTime" content="2014-11-03T00:00:00-05:00" class="date-display-single">November 3, 2014</span></p><div class='syndicate'><h1>Clinical Exome Sequencing Detects Disease-Causing Glitches</h1><div class="callout callout-with-border"><h3>At a Glance</h3>
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<ul class="spaced">
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<li>In some patients with suspected genetic conditions, a fast, powerful technique called whole-exome sequencing provided a molecular diagnosis.</li>
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<li>The new tool can help doctors pinpoint the underlying causes of many rare and hard-to-diagnose genetic conditions.</li>
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-large/public/news-events/research-matters/2014/20141103-exome.jpg?itok=uUbMVQf-&timestamp=1431544174 1x" media="screen and (min-width: 960px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium/public/news-events/research-matters/2014/20141103-exome.jpg?itok=XxRJBFEL&timestamp=1431544174 1x" media="screen and (min-width: 800px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium-small/public/news-events/research-matters/2014/20141103-exome.jpg?itok=Yvz7wc2T&timestamp=1431544174 1x" media="screen and (min-width: 600px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-small/public/news-events/research-matters/2014/20141103-exome.jpg?itok=c9Hrw-BB&timestamp=1431544174 1x" media="screen and (min-width: 480px)" />
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<source srcset="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-tiny/public/news-events/research-matters/2014/20141103-exome.jpg?itok=XUqaTbJu&timestamp=1431544174 1x" media="screen and (min-width: 0)" />
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<img src="https://www.nih.gov/sites/default/files/styles/floated_media_breakpoint-medium/public/news-events/research-matters/2014/20141103-exome.jpg?itok=XxRJBFEL&timestamp=1431544174" alt="Mother and son." title="Mother and son" />
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</picture><span class="caption">Audrey Lapidus and her son, Calvin, who was diagnosed with a rare genetic disorder after months of inconclusive tests stumped doctors. The UCLA Clinical Genomics Center sequenced his DNA to identify the single mutation causing his baffling symptoms.</span><span class="credit">Lapidus Family</span></div>
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</div><p>For people with suspected rare genetic conditions, getting an accurate diagnosis can be difficult and frustrating. Doctors can find it challenging to match a complicated set of symptoms to the thousands of known genetic conditions. Yet determining the cause of a condition is a critical step in developing a treatment plan and anticipating whether additional medical problems are likely to develop. It can also help the family understand the risk to other family members.</p>
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<p>Genetic sequencing is expected to greatly improve the rate of diagnoses for rare conditions in the future. In contrast to whole-genome sequencing, which analyzes the 3 billion base pairs in the human genome, whole-exome sequencing focuses on the DNA in the 1% of the human genome that codes for proteins. Most disease-causing, single-gene mutations are located in these areas.</p>
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<p>In 2 NIH-supported studies, different research teams analyzed the results of whole-exome sequencing in a clinical setting. The scientists evaluated the exomes of a total of nearly 3,000 people suspected of having a genetic disorder. Most were pediatric patients under age 18. In many cases, their parents’ genetic sequences were also assessed. Despite sometimes years of medical consultation and testing, none of these patients had yet received a definitive diagnosis.</p>
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<p>As reported in the October 18, 2014, online edition of the <em>Journal of the American Medical Association</em>, both studies found that whole-exome sequencing led to a potential molecular diagnosis for about 1 in 4 participants.</p>
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||
<p>One study evaluated 2,000 people who were referred by physicians to the Baylor College of Medicine for clinical whole-exome sequencing. In 504 cases (25%), the researchers detected variants in known disease-causing genes that appeared to be aligned with the patients’ symptoms. More than half (53%) of the disease-linked conditions were autosomal dominant, meaning they likely arose from just one abnormal gene. In nearly 75% of these cases, the abnormal variant was new (“de novo”), meaning it wasn’t inherited from either parent. The scientists also found that 5% of subjects with diagnoses carried 2 different genetic diseases.</p>
|
||
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||
<p>The other study analyzed the exomes of 814 patients referred to the genomics center at the University of California, Los Angeles. Clinical sequencing resulted in a molecular diagnosis for 213 patients (26%). Diagnostic rates were higher (31%) for the subset of patients whose parents’ exomes were also sequenced (127 of 410 cases).</p>
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||
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<p>Both research teams note that additional studies will be needed to validate their findings. Further work will also be needed to determine how genomic sequencing can best be applied in clinical situations.</p>
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<p>“I expect that in a few years, we will learn of the importance of whole-exome sequencing in adult medicine and in fields of pediatrics outside of development,” says Baylor’s Dr. Sharon Plon, a coauthor of the first study. “We are currently performing an NIH-supported clinical trial of whole exome sequencing in childhood cancer patients to learn of its potential utility for these patients.”</p>
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<p>—by Vicki Contie</p>
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</div><h2 class="label-above">Related Links</h2><ul class="spaced print-urls"><li><a href="http://www.nih.gov/researchmatters/march2014/03032014syndrome.htm" target="_top">Rare Syndrome in Children Explained</a></li><li><a href="http://www.nih.gov/researchmatters/august2010/08232010kabuki.htm" target="_top">Kabuki Syndrome Gene Identified</a></li><li><a href="http://www.nih.gov/researchmatters/march2010/03222010genome.htm" target="_top">Whole-Genome Analyses Pinpoint Disease Genes in Families</a></li><li><a href="http://www.genome.gov/17515946" target="_top">Learning About An Undiagnosed Condition in an Adult</a></li></ul><p class="footnote"><strong class="label-inline">References: </strong><a href="http://www.ncbi.nlm.nih.gov/pubmed/25326637">Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders.</a> Lee H, Deignan JL, Dorrani N, Strom SP, Kantarci S, Quintero-Rivera F, Das K, Toy T, Harry B, Yourshaw M, Fox M, Fogel BL, Martinez-Agosto JA, Wong DA, Chang VY, Shieh PB, Palmer CG, Dipple KM, Grody WW, Vilain E, Nelson SF. <em>JAMA</em><em>.</em> 2014 Oct 18. doi: 10.1001/jama.2014.14604. [Epub ahead of print]. PMID: 25326637.
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||
<a href="http://www.ncbi.nlm.nih.gov/pubmed/25326635">Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing.</a> Yang Y, Muzny DM, Xia F, Niu Z, Person R, Ding Y, Ward P, Braxton A, Wang M, Buhay C, Veeraraghavan N, Hawes A, Chiang T, Leduc M, Beuten J, Zhang J, He W, Scull J, Willis A, Landsverk M, Craigen WJ, Bekheirnia MR, Stray-Pedersen A, Liu P, Wen S, Alcaraz W, Cui H, Walkiewicz M, Reid J, Bainbridge M, Patel A, Boerwinkle E, Beaudet AL, Lupski JR, Plon SE, Gibbs RA, Eng CM. <em>JAMA</em><em>.</em> 2014 Oct 18. doi: 10.1001/jama.2014.14601. [Epub ahead of print]. PMID: 25326635.</p><p class="footnote"><strong class="label-inline">Funding: </strong>NIH’s National Center for Advancing Translational Science (NCATS), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Human Genome Research Institute (NHGRI), National Institute of Neurological Disorders and Stroke (NINDS), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD); the California Institute of Regenerative Medicine; and Hyundai Hope on Wheels Scholar Award.</p>
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NIH Research Matters<br />
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<p><a href="https://www.nih.gov/news-events/nih-research-matters/research-context-can-we-slow-aging">Research in Context: Can we slow aging?</a></p>
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<p><a href="https://www.nih.gov/news-events/nih-research-matters/brain-changes-observed-during-pregnancy">Brain changes observed during pregnancy</a></p>
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<p><a href="https://www.nih.gov/news-events/nih-research-matters/research-context-detecting-cancer">Research in Context: Detecting cancer</a></p>
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<p><a href="https://www.nih.gov/news-events/nih-research-matters/risk-future-burden-dementia-united-states">Risk and future burden of dementia in the United States </a></p>
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<p><a href="https://www.nih.gov/news-events/nih-research-matters/complete-wiring-map-adult-fruit-fly-brain">Complete wiring map of an adult fruit fly brain</a></p>
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<p><strong>Assistant Editors:</strong> Vicki Contie and Brian Doctrow, Ph.D.</p>
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<p><strong><em>NIH Research Matters </em></strong>is a weekly update of NIH research highlights reviewed by NIH’s experts. It's published by the <a href="/institutes-nih/nih-office-director/office-communications-public-liaison">Office of Communications and Public Liaison</a> in the <a href="/institutes-nih/nih-office-director">NIH Office of the Director</a>.</p>
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