Prevalence rates of Kawasaki disease (KD) are increasing among children in Asia, the
United States and Western Europe.
Kawasaki disease is the most common acquired heart disease in
children. Untreated, roughly one-quarter of children with KD develop
coronary artery aneurysms - balloon-like bulges of heart vessels -
that may ultimately result in heart attacks, congestive heart failure or
‘A novel whole genome sequencing of a family in which two of four children were affected by Kawasaki disease (KD) has revealed plausible gene variants that predispose some children to developing the disease.
The causative agent for KD remains unknown - a windborne pathogen
is suspected - but equally mysterious is why and how some children are
Researchers at University of California San Diego
School of Medicine, with colleagues at Rady Children's Institute for
Genomic Medicine and in London and Singapore, have conducted novel whole
genome sequencing of a family in which two of four children were
affected by KD. They have identified plausible gene variants that
predispose some children to developing the disease.
The findings were recently published in the PLOS ONE
"This is the first successful analysis of whole genome sequence from
a family that revealed a new gene implicated in KD susceptibility,"
said senior author Jane C. Burns, professor and director of the
Kawasaki Disease Research Center at UC San Diego School of Medicine and
Rady Children's Hospital-San Diego.
"The finding is intriguing because
this gene, a member of the Toll-like receptor family, encodes for a
protein that is expressed on the cell surface and uniquely binds to
proteins outside the cell that come from fungi. This may be a clue that
fungal antigens could be one environmental trigger for the disease."
In Japan, the country with the highest
incidence: 306 out of every 100,000 children under the age of five,
with more than 14,000 new cases annually. One in every 60 boys and one
in every 75 girls in Japan will develop KD during childhood.
Incidence rates in the United States are lower - nine to 19 per
100,000 children under age five - but rising, at least in San Diego
County. Predictive models estimate that by 2030, one in every 1,600
American adults will have been affected by the disease.
KD has a clear genetic link. It is most common in the U.S. among
persons of Asian or African descent, but its genetics is complex and
researchers have struggled to identify which gene variants and
combinations cause some children to develop the disease. Burns and
colleagues employed analysis of whole genome sequence for the first time
to examine a six-member African-American family in which two children
had KD, but the parents and other siblings did not.
"Despite their apparent increased susceptibility, children of
African-American descent have been excluded from previous KD genetic
analysis," the authors wrote.
Key among the tools used was whole genome sequencing, a process in
which the complete DNA sequence of a person's genome is determined at a
single time. The researchers also looked at genome-wide association
studies, which search for genetic variation in large populations. The
goal was to find, if possible, distinct gene variants that, in
combination, might indicate predisposition to and higher likelihood of
The researchers identified a variation of the toll-like receptor 6
gene, which plays a fundamental role in the immune system, that may be
linked to the pro-inflammatory state during the acute stage of KD.
Previous research had not identified this gene as influencing
susceptibility to KD.
In addition, another variant in a gene called tumor-associated
calcium signal transducer 2, which is involved in cellular calcium
signaling, was highlighted. The authors said further investigation of
TACSTD2 is needed.
Burns said the study, with its analytic approach and use of whole
genome sequencing, represents a new method for uncovering relevant gene
variants in families affected by not just KD, but many other complex
"The analysis of whole genome sequence to understand disease
genetics is only recently becoming a tool that is affordable and
manageable due to new developments in computer science. We are excited
to be learning how to harness the power of this analysis to study our
children," Burns said.
"Our next approach will be to compare the whole genome sequence from
KD patients with severe heart damage to those with no damage despite no
or delayed treatment. We hope this will lead us to the genetic pathways
that result in damage to the coronary arteries, which in turn will
suggest new therapies to target those pathways."