The impact of down-regulated SK3 expressions on Hirschsprung disease

BMC Med Genet. 2018 Feb 13;19(1):24. doi: 10.1186/s12881-018-0539-3.

Abstract

Background: Some Hirschsprung's disease (HSCR) patients showed persistent bowel symptoms following an appropriately performed pull-through procedure. The mechanism is presumed to be down-regulated small-conductance calcium-activated potassium channel 3 (SK3) expression in the HSCR ganglionic intestines. We aimed to investigate the SK3 expression's impact in HSCR patients after a properly performed pull-through surgery in an Indonesian population, a genetically distinct group within Asia.

Methods: We assessed SK3 gene expression in both the ganglionic and aganglionic colon of HSCR patients and controls colon by quantitative real-time polymerase chain reaction (RT-PCR).

Results: We ascertained fourteen sporadic HSCR patients and six anorectal malformation patients as controls. Quantitative RT-PCR showed that the SK3 expression was significantly lower (23-fold) in the ganglionic colon group compared to the control group (9.9 ± 4.6 vs. 5.4 ± 3.4; p = 0.044). The expression of SK3 in the aganglionic colon group was also significantly lower (43-fold) compared to the control group (10.8 ± 4.4 vs. 5.4 ± 3.4; p = 0.015).

Conclusion: Our study shows that the down-regulated SK3 expression in ganglionic intestines might contribute to the persistent bowel symptoms following a properly performed pull-through surgery in Indonesian HSCR patients. Furthermore, this study is the first report of SK3 expression in a sample population of Asian ancestry.

Keywords: Appropriate pull-through; Hirschsprung disease; Indonesia; Persistent bowel symptoms; SK3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anorectal Malformations / diagnosis
  • Anorectal Malformations / genetics
  • Asian People / genetics
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Colon / metabolism
  • Down-Regulation*
  • Follow-Up Studies
  • Genotyping Techniques
  • Hirschsprung Disease / diagnosis
  • Hirschsprung Disease / genetics*
  • Humans
  • Indonesia
  • Infant
  • Real-Time Polymerase Chain Reaction
  • Small-Conductance Calcium-Activated Potassium Channels / genetics*
  • Small-Conductance Calcium-Activated Potassium Channels / metabolism

Substances

  • KCNN3 protein, human
  • Small-Conductance Calcium-Activated Potassium Channels