NELFCD and CTSZ loci are associated with jaundice-stage progression in primary biliary cholangitis in the Japanese population.
Nao NishidaYoshihiro AibaYuki HitomiMinae KawashimaKaname KojimaYosuke KawaiKazuko UenoHitomi NakamuraNoriyo YamashikiTomohiro TanakaSumito TamuraAkira MoriShintaro YagiYuji SoejimaTomoharu YoshizumiMitsuhisa TakatsukiAtsushi TanakaKenichi HaradaShinji ShimodaAtsumasa KomoriSusumu EguchiYoshihiko MaeharaShinji UemotoNorihiro KokudoMasao NagasakiKatsushi TokunagaMinoru NakamuraPublished in: Scientific reports (2018)
Approximately 10-20% of patients with primary biliary cholangitis (PBC) progress to jaundice stage regardless of treatment with ursodeoxycholic acid and bezafibrate. In this study, we performed a GWAS and a replication study to identify genetic variants associated with jaundice-stage progression in PBC using a total of 1,375 patients (1,202 early-stage and 173 jaundice-stage) in a Japanese population. SNP rs13720, which is located in the 3'UTR of cathepsin Z (CTSZ), showed the strongest association (odds ratio [OR] = 2.15, P = 7.62 × 10-7) with progression to jaundice stage in GWAS. High-density association mapping at the CTSZ and negative elongation factor complex member C/D (NELFCD) loci, which are located within a strong linkage disequilibrium (LD) block, revealed that an intronic SNP of CTSZ, rs163800, was significantly associated with jaundice-stage progression (OR = 2.16, P = 8.57 × 10-8). In addition, eQTL analysis and in silico functional analysis indicated that genotypes of rs163800 or variants in strong LD with rs163800 influence expression levels of both NELFCD and CTSZ mRNA. The present novel findings will contribute to dissect the mechanism of PBC progression and also to facilitate the development of therapies for PBC patients who are resistant to current therapies.
Keyphrases
- high density
- genome wide
- end stage renal disease
- early stage
- newly diagnosed
- chronic kidney disease
- ejection fraction
- prognostic factors
- high resolution
- binding protein
- copy number
- radiation therapy
- mass spectrometry
- gene expression
- hepatitis c virus
- locally advanced
- neoadjuvant chemotherapy
- molecular docking
- rectal cancer