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A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome.

Publication ,  Journal Article
Bradley, MS; Burke, EE; Grenier, C; Amundsen, CL; Murphy, SK; Siddiqui, NY
Published in: Neurourol Urodyn
April 2018

AIMS: To assess the feasibility of using voided urine samples to perform a DNA methylation study in females with interstitial cystitis/bladder pain syndrome (IC/BPS) as compared to age- and race-matched controls. A unique methylation profile could lead to a non-invasive, reproducible, and objective biomarker that would aid clinicians in the diagnosis of IC/BPS. METHODS: Nineteen IC/BPS patients and 17 controls were included. IC/BPS patients had an Interstitial Cystitis Symptom Index score of >8; controls had no bladder symptoms. DNA was extracted from pelleted urine sediment. Samples with >500 ng of genomic DNA underwent quantitative DNA methylation assessment using the Illumina Infinium MethylationEPIC BeadChip. Age- and race-matching was applied prior to analysis. Linear regression models were used to compare average methylation between IC/BPS cases and controls at each cytosine guanine dinucleotide site (loci where methylation can occur). RESULTS: Sixteen participants (eight IC/BPS age- and race-matched to eight controls) had adequate DNA for methylation analysis. The median age was 43.5 years (interquartile range 33.8, 65.0), the median BMI was 27.1 (IQR 22.7, 31.4), and 14 were Caucasian (87.5%). A total of 688 417 CpG sites were analyzed. In exploratory pathway analysis utilizing the top 1000 differentially methylated CpG sites, the mitogen-activated protein kinase (MAPK) pathway was overrepresented by member genes. CONCLUSIONS: The results demonstrate the feasibility of using voided urine specimens from women with IC/BPS to perform DNA methylation assessments. Additionally, the data suggest genes within or downstream of the MAPK pathway exhibit altered methylation in IC/BPS.

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Published In

Neurourol Urodyn

DOI

EISSN

1520-6777

Publication Date

April 2018

Volume

37

Issue

4

Start / End Page

1485 / 1493

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Pelvic Pain
  • Middle Aged
  • Humans
  • Female
  • Feasibility Studies
  • DNA Methylation
  • Cystitis, Interstitial
  • Biomarkers
  • Aged
 

Citation

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Bradley, M. S., Burke, E. E., Grenier, C., Amundsen, C. L., Murphy, S. K., & Siddiqui, N. Y. (2018). A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome. Neurourol Urodyn, 37(4), 1485–1493. https://doi.org/10.1002/nau.23489
Bradley, Megan S., Emily E. Burke, Carole Grenier, Cindy L. Amundsen, Susan K. Murphy, and Nazema Y. Siddiqui. “A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome.Neurourol Urodyn 37, no. 4 (April 2018): 1485–93. https://doi.org/10.1002/nau.23489.
Bradley MS, Burke EE, Grenier C, Amundsen CL, Murphy SK, Siddiqui NY. A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome. Neurourol Urodyn. 2018 Apr;37(4):1485–93.
Bradley, Megan S., et al. “A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome.Neurourol Urodyn, vol. 37, no. 4, Apr. 2018, pp. 1485–93. Pubmed, doi:10.1002/nau.23489.
Bradley MS, Burke EE, Grenier C, Amundsen CL, Murphy SK, Siddiqui NY. A genome-scale DNA methylation study in women with interstitial cystitis/bladder pain syndrome. Neurourol Urodyn. 2018 Apr;37(4):1485–1493.
Journal cover image

Published In

Neurourol Urodyn

DOI

EISSN

1520-6777

Publication Date

April 2018

Volume

37

Issue

4

Start / End Page

1485 / 1493

Location

United States

Related Subject Headings

  • Urology & Nephrology
  • Pelvic Pain
  • Middle Aged
  • Humans
  • Female
  • Feasibility Studies
  • DNA Methylation
  • Cystitis, Interstitial
  • Biomarkers
  • Aged