Kawasaki disease pathophysiology: Difference between revisions
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==Genetics== | ==Genetics== | ||
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* | Genes Implicated in Susceptibility to KD With Replication in Independent Cohorts | ||
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| colspan="2" |<small>Adapted from the AHA Scientific Statement on the diagnosis, treatment, and long term management of Kawasaki disease</small><ref name="McCrindleRowley2017">{{cite journal|last1=McCrindle|first1=Brian W.|last2=Rowley|first2=Anne H.|last3=Newburger|first3=Jane W.|last4=Burns|first4=Jane C.|last5=Bolger|first5=Anne F.|last6=Gewitz|first6=Michael|last7=Baker|first7=Annette L.|last8=Jackson|first8=Mary Anne|last9=Takahashi|first9=Masato|last10=Shah|first10=Pinak B.|last11=Kobayashi|first11=Tohru|last12=Wu|first12=Mei-Hwan|last13=Saji|first13=Tsutomu T.|last14=Pahl|first14=Elfriede|title=Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association|journal=Circulation|volume=135|issue=17|year=2017|pages=e927–e999|issn=0009-7322|doi=10.1161/CIR.0000000000000484}}</ref> | |||
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! colspan="1" rowspan="1" |Gene | |||
! colspan="1" rowspan="1" |Chromosome Location | |||
! colspan="1" rowspan="1" |Genetic Methods | |||
! colspan="1" rowspan="1" |Validation Populations | |||
! colspan="1" rowspan="1" |Potential Significance | |||
! colspan="1" rowspan="1" |Reference and Year | |||
|- | |||
| colspan="1" rowspan="1" |''FCGR2A'' | |||
| colspan="1" rowspan="1" |1q23 | |||
| colspan="1" rowspan="1" |GWAS | |||
| colspan="1" rowspan="1" |European descent, Taiwanese, Koreans, Han Chinese | |||
| colspan="1" rowspan="1" |Low-affinity receptor for Fc fragment of IgG; risk allele has lower binding affinity | |||
| colspan="1" rowspan="1" |Khor et al61 2011 | |||
|- | |||
| colspan="1" rowspan="1" |''CASP3'' | |||
| colspan="1" rowspan="1" |4q34-35 | |||
| colspan="1" rowspan="1" |Linkage analysis | |||
Candidate gene study | |||
| colspan="1" rowspan="1" |Japanese, Taiwanese, Koreans, Chinese, Euro-Americans | |||
| colspan="1" rowspan="1" |Mediates apoptosis in immune cells and cardiomyocytes | |||
Risk allele decreases gene transcription | |||
| colspan="1" rowspan="1" |Onouchi et al62 2010 | |||
|- | |||
| colspan="1" rowspan="1" |''HLA''class II | |||
| colspan="1" rowspan="1" |6p21.3 | |||
| colspan="1" rowspan="1" |GWAS | |||
| colspan="1" rowspan="1" |Japanese, Taiwanese, Koreans | |||
| colspan="1" rowspan="1" |Activation marker for immune cells; antigen presentation | |||
| colspan="1" rowspan="1" |Onouchi et al63 2012 | |||
|- | |||
| colspan="1" rowspan="1" |''BLK'' | |||
| colspan="1" rowspan="1" |8p23-22 | |||
| colspan="1" rowspan="1" |GWAS | |||
| colspan="1" rowspan="1" |Japanese, Taiwanese, Koreans | |||
| colspan="1" rowspan="1" |B-cell receptor signal transduction | |||
| colspan="1" rowspan="1" |Onouchi et al63 2012 | |||
|- | |||
| colspan="1" rowspan="1" |''IPTKC'' | |||
| colspan="1" rowspan="1" |19q13.2 | |||
| colspan="1" rowspan="1" |Linkage analysis | |||
TDT | |||
| colspan="1" rowspan="1" |Japanese, Taiwanese, Koreans, Chinese, Euro- Americans | |||
| colspan="1" rowspan="1" |Negative regulator of calcineurin-NFAT signaling pathway; risk allele increases signaling | |||
| colspan="1" rowspan="1" |Onouchi et al64 2008 | |||
|- | |||
| colspan="1" rowspan="1" |''CD40'' | |||
| colspan="1" rowspan="1" |20q12-13.2 | |||
| colspan="1" rowspan="1" |GWAS | |||
| colspan="1" rowspan="1" |Japanese, Taiwanese, Koreans | |||
| colspan="1" rowspan="1" |Risk alleles associated with increased translation | |||
| colspan="1" rowspan="1" |Onouchi et al63 2012 | |||
|} | |||
* BLK indicates B-cell lymphoid kinase; CASP3, caspase 3; FCGR, Fcγ receptor; GWAS, genome-wide association study; HLA, human leukocyte antigen; IgG, immunoglobulin G; ITPKC, inositol 1,4,5-trisphosphate kinase-C; KD, Kawasaki disease; NFAT, nuclear factor of activated T cells; and TDT, transmission disequilibrium test. | |||
==Associated Conditions== | ==Associated Conditions== |
Revision as of 18:37, 10 April 2018
Kawasaki disease Microchapters |
Diagnosis |
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Treatment |
Case Studies |
American Roentgen Ray Society Images of Kawasaki disease pathophysiology |
Risk calculators and risk factors for Kawasaki disease pathophysiology |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
The exact pathogenesis of [disease name] is not fully understood.
OR
It is thought that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
OR
[Pathogen name] is usually transmitted via the [transmission route] route to the human host.
OR
Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
OR
[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
OR
The progression to [disease name] usually involves the [molecular pathway].
OR
The pathophysiology of [disease/malignancy] depends on the histological subtype.
Pathophysiology
Pathogenesis
- The exact pathogenesis of [disease name] is not fully understood.
OR
- It is understood that [disease name] is the result of / is mediated by / is produced by / is caused by either [hypothesis 1], [hypothesis 2], or [hypothesis 3].
- [Pathogen name] is usually transmitted via the [transmission route] route to the human host.
- Following transmission/ingestion, the [pathogen] uses the [entry site] to invade the [cell name] cell.
- [Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
- The progression to [disease name] usually involves the [molecular pathway].
- The pathophysiology of [disease/malignancy] depends on the histological subtype.
Genetics
.
Genes Implicated in Susceptibility to KD With Replication in Independent Cohorts
Adapted from the AHA Scientific Statement on the diagnosis, treatment, and long term management of Kawasaki disease[1] | |||||
Gene | Chromosome Location | Genetic Methods | Validation Populations | Potential Significance | Reference and Year |
---|---|---|---|---|---|
FCGR2A | 1q23 | GWAS | European descent, Taiwanese, Koreans, Han Chinese | Low-affinity receptor for Fc fragment of IgG; risk allele has lower binding affinity | Khor et al61 2011 |
CASP3 | 4q34-35 | Linkage analysis
Candidate gene study |
Japanese, Taiwanese, Koreans, Chinese, Euro-Americans | Mediates apoptosis in immune cells and cardiomyocytes
Risk allele decreases gene transcription |
Onouchi et al62 2010 |
HLAclass II | 6p21.3 | GWAS | Japanese, Taiwanese, Koreans | Activation marker for immune cells; antigen presentation | Onouchi et al63 2012 |
BLK | 8p23-22 | GWAS | Japanese, Taiwanese, Koreans | B-cell receptor signal transduction | Onouchi et al63 2012 |
IPTKC | 19q13.2 | Linkage analysis
TDT |
Japanese, Taiwanese, Koreans, Chinese, Euro- Americans | Negative regulator of calcineurin-NFAT signaling pathway; risk allele increases signaling | Onouchi et al64 2008 |
CD40 | 20q12-13.2 | GWAS | Japanese, Taiwanese, Koreans | Risk alleles associated with increased translation | Onouchi et al63 2012 |
- BLK indicates B-cell lymphoid kinase; CASP3, caspase 3; FCGR, Fcγ receptor; GWAS, genome-wide association study; HLA, human leukocyte antigen; IgG, immunoglobulin G; ITPKC, inositol 1,4,5-trisphosphate kinase-C; KD, Kawasaki disease; NFAT, nuclear factor of activated T cells; and TDT, transmission disequilibrium test.
Associated Conditions
Gross Pathology
- On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Microscopic Pathology
- On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
References
- ↑ McCrindle, Brian W.; Rowley, Anne H.; Newburger, Jane W.; Burns, Jane C.; Bolger, Anne F.; Gewitz, Michael; Baker, Annette L.; Jackson, Mary Anne; Takahashi, Masato; Shah, Pinak B.; Kobayashi, Tohru; Wu, Mei-Hwan; Saji, Tsutomu T.; Pahl, Elfriede (2017). "Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association". Circulation. 135 (17): e927–e999. doi:10.1161/CIR.0000000000000484. ISSN 0009-7322.