Whole Genome Study Reveals Clues To Solving The Mystery Behind Kawasaki Disease

Main Category: Genetics
Also Included In: Pediatrics / Children's Health
Article Date: 09 Jan 2009 - 2:00 PDT

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A study looking at the entire human genome has identified new genes that appear to be involved in making some children more susceptible to Kawasaki disease, according to a new international study published January 9 in the open-access journal PLoS Genetics. The research team, from The University of Western Australia, the Genome Institute of Singapore, Emma Children's Hospital, The Netherlands, Imperial College London, UK and the University of California San Diego, USA studied naturally occurring genetic variation in almost 900 cases of Kawasaki disease from these countries.

Kawasaki disease is an inflammatory condition in children that affects the mucus membranes, lymph nodes, walls of blood vessels, and the heart. Clinical signs include high fever, rash, and swollen hands and feet with skin peeling. Most importantly, the disease causes damage to the coronary arteries in a quarter of untreated children and may increase the risk of atherosclerosis in early adulthood. The cause of Kawasaki disease is unknown; an infectious etiology is suspected but not proven. There is no diagnostic test and current treatment fails to prevent coronary damage in at least 1 in 10 to 20 children. Kawasaki disease is fatal in approximately 1 in 1000 children.

This is the first genetic study of an infectious disease to examine the whole genome, rather than selected genes. The study shows that genes involved in cardiovascular function and inflammation may be particularly important and some seem to function together. The authors believe these findings could lead to new diagnostics and better treatment and may offer information about adult cardiovascular disease as well.

However, the findings do not yet prove that the new genes are functionally involved. Other genetic variants may be important, especially in different ethnic groups. The authors are now planning detailed studies of the function of these genes and larger collaborative studies including East Asian populations, who are at particular risk of Kawasaki disease, with 1 in 150 Japanese children affected.

CITATION:
A Genome-Wide Association Study Identifies Novel and Functionally Related Susceptibility Loci for Kawasaki Disease.
Burgner D, Davila S, Breunis WB, Ng SB, Li Y, et al. (2009)
PLoS Genet 5(1): e1000319. doi:10.1371/journal.pgen.1000319
Click here to view article online.

About PLoS Genetics

PLoS Genetics reflects the full breadth and interdisciplinary nature of genetics and genomics research by publishing outstanding original contributions in all areas of biology. All works published in PLoS Genetics are open access. Everything is immediately and freely available online throughout the world subject only to the condition that the original authorship and source are properly attributed. Copyright is retained by the authors. The Public Library of Science uses the Creative Commons Attribution License.

PLoS Genetics

About the Public Library of Science

The Public Library of Science (PLoS) is a non-profit organization of scientists and physicians committed to making the world's scientific and medical literature a freely available public resource.

Public Library of Science

Article adapted by Medical News Today from original press release.
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Public Library of Science. "Whole Genome Study Reveals Clues To Solving The Mystery Behind Kawasaki Disease." Medical News Today. MediLexicon, Intl., 9 Jan. 2009. Web.
13 Feb. 2012. <http://www.medicalnewstoday.com/releases/134906.php>

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Public Library of Science. (2009, January 9). "Whole Genome Study Reveals Clues To Solving The Mystery Behind Kawasaki Disease." Medical News Today. Retrieved from
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