Abstract | BACKGROUND: METHODS: To explore genetic variants related to IVIG-unresponsiveness, we designated KD patients who did not respond to both first and second courses of IVIG therapy as IVIG-unresponsive patients. Using genomic DNA from 30 IVIG-unresponsive KD patients, we performed pooled genome sequencing targeting 39 immune-related cytokine receptor genes. RESULTS: The single nucleotide variant (SNV), rs563535954 (located in the IL4R locus), was concentrated in IVIG-unresponsive KD patients. Individual genotyping showed that the minor allele of rs563535954 was present in 4/33 patients with IVIG-unresponsive KD, compared with 20/1063 individuals in the Japanese genome variation database (odds ratio = 7.19, 95% confidence interval 2.43-21.47). Furthermore, the minor allele of rs563535954 was absent in 42 KD patients who responded to IVIG treatment (P = 0.0337), indicating that a low-frequency variant, rs563535954, is associated with IVIG-unresponsiveness in KD patients. Although rs563535954 is located in the 3'-untranslated region of IL4R, there was no alternation in IL4R expression associated with the mior allele of rs563535954. However, IVIG-unresponsive patients that exhibited the minor allele of rs563535954 tended to be classified into the low-risk group (based on previously reported risk scores) for prediction of IVIG-resistance. Therefore, IVIG-unresponsiveness associated with the minor allele of rs563535954 might differ from IVIG-unresponsiveness associated with previous risk factors used to evaluate IVIG-unresponsiveness in KD. CONCLUSION: These findings suggest that the SNV rs563535954 could serve as a predictive indicator of IVIG-unresponsiveness, thereby improving the sensitivity of risk scoring systems, and may aid in prevention of coronary artery lesions in KD patients.
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Authors | Yuji Amano, Yohei Akazawa, Jun Yasuda, Kazuhisa Yoshino, Katsuhiko Kojima, Norimoto Kobayashi, Satoshi Matsuzaki, Masao Nagasaki, Yosuke Kawai, Naoko Minegishi, Noriko Ishida, Noriko Motoki, Akira Hachiya, Yozo Nakazawa, Masayuki Yamamoto, Kenichi Koike, Toshikazu Takeshita |
Journal | Pediatric rheumatology online journal
(Pediatr Rheumatol Online J)
Vol. 17
Issue 1
Pg. 34
(Jul 03 2019)
ISSN: 1546-0096 [Electronic] England |
PMID | 31269967
(Publication Type: Journal Article)
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Chemical References |
- IL4R protein, human
- Immunoglobulins, Intravenous
- Interleukin-4 Receptor alpha Subunit
- RNA, Messenger
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Topics |
- Child
- Child, Preschool
- Coronary Artery Disease
(genetics)
- Drug Resistance
(genetics)
- Female
- Gene Expression Profiling
- Gene Frequency
- Genome-Wide Association Study
- Humans
- Immunoglobulins, Intravenous
(therapeutic use)
- Infant
- Interleukin-4 Receptor alpha Subunit
(genetics)
- Japan
(ethnology)
- Male
- Mucocutaneous Lymph Node Syndrome
(drug therapy, genetics)
- Polymorphism, Single Nucleotide
(genetics)
- RNA, Messenger
(genetics)
- Sequence Analysis, RNA
- Treatment Failure
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