Elevated fecal M2‐pyruvate kinase in children with cystic fibrosis: A clue to the increased risk of intestinal malignancy in adulthood?. Issue 5 (May 2015)
- Record Type:
- Journal Article
- Title:
- Elevated fecal M2‐pyruvate kinase in children with cystic fibrosis: A clue to the increased risk of intestinal malignancy in adulthood?. Issue 5 (May 2015)
- Main Title:
- Elevated fecal M2‐pyruvate kinase in children with cystic fibrosis: A clue to the increased risk of intestinal malignancy in adulthood?
- Authors:
- Pang, Tamara
Leach, Steven T
Katz, Tamarah
Jaffe, Adam
Day, Andrew S
Ooi, Chee Y - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12842-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Adult patients with cystic fibrosis (CF) have an increased risk of gastrointestinal malignancies. We hypothesized that increased intestinal cell turnover beginning in childhood may explain the increased risk of malignancy in early adulthood. Therefore, we aimed to measure fecal M2‐pyruvate kinase (M2‐PK), a biomarker of intestinal cell turnover, in children with CF. To assess whether the increased cell turnover is secondary to intestinal inflammation, the secondary aims were to measure fecal calprotectin and evaluate its association with fecal M2‐PK.</p> </sec> <sec id="jgh12842-sec-0002" sec-type="section"> <title>Methods</title> <p>Fecal samples, for M2‐PK and calprotectin measurements, were prospectively collected from children with CF and healthy controls (HC).</p> </sec> <sec id="jgh12842-sec-0003" sec-type="section"> <title>Results</title> <p>Thirty‐three children with CF (mean [standard deviation] 7.3 [3.8] years old; 29 pancreatic insufficient [PI]) were enrolled and compared with 33 age‐matched HC. Fecal M2‐PK in CF patients (median [interquartile range, IQR]: 4.7 [1.5–9.7]) was greater than HC (1.0 [1.0–1.0] U/mL; <italic>P</italic> &lt; 0.0001), and higher in PI (median [IQR]: 5.1 [1.8–13.7]) than pancreatic sufficient patients (1.0 [1.0–1.0] U/mL; <italic>P</italic> = 0.002). Fecal calprotectin was significantly elevated in<abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12842-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>Adult patients with cystic fibrosis (CF) have an increased risk of gastrointestinal malignancies. We hypothesized that increased intestinal cell turnover beginning in childhood may explain the increased risk of malignancy in early adulthood. Therefore, we aimed to measure fecal M2‐pyruvate kinase (M2‐PK), a biomarker of intestinal cell turnover, in children with CF. To assess whether the increased cell turnover is secondary to intestinal inflammation, the secondary aims were to measure fecal calprotectin and evaluate its association with fecal M2‐PK.</p> </sec> <sec id="jgh12842-sec-0002" sec-type="section"> <title>Methods</title> <p>Fecal samples, for M2‐PK and calprotectin measurements, were prospectively collected from children with CF and healthy controls (HC).</p> </sec> <sec id="jgh12842-sec-0003" sec-type="section"> <title>Results</title> <p>Thirty‐three children with CF (mean [standard deviation] 7.3 [3.8] years old; 29 pancreatic insufficient [PI]) were enrolled and compared with 33 age‐matched HC. Fecal M2‐PK in CF patients (median [interquartile range, IQR]: 4.7 [1.5–9.7]) was greater than HC (1.0 [1.0–1.0] U/mL; <italic>P</italic> &lt; 0.0001), and higher in PI (median [IQR]: 5.1 [1.8–13.7]) than pancreatic sufficient patients (1.0 [1.0–1.0] U/mL; <italic>P</italic> = 0.002). Fecal calprotectin was significantly elevated in CF than HC (median [IQR] 61.3 [43.8–143.8] <italic>vs</italic> 19.5 [19.5–35.1] mg/kg; <italic>P</italic> &lt; 0.0001). However, there was no correlation between fecal M2‐PK and fecal calprotectin levels among subjects with CF (<italic>r</italic> = 0.29; <italic>P</italic> = 0.1).</p> </sec> <sec id="jgh12842-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Increased intestinal cell turnover is present in children with PI CF. The lack of relationship between fecal M2‐PK and calprotectin suggests that contributing factor(s) other than inflammation may be present.</p> </sec> </abstract> … (more)
- Is Part Of:
- Journal of gastroenterology and hepatology. Volume 30:Issue 5(2015:May)
- Journal:
- Journal of gastroenterology and hepatology
- Issue:
- Volume 30:Issue 5(2015:May)
- Issue Display:
- Volume 30, Issue 5 (2015)
- Year:
- 2015
- Volume:
- 30
- Issue:
- 5
- Issue Sort Value:
- 2015-0030-0005-0000
- Page Start:
- 866
- Page End:
- 871
- Publication Date:
- 2015-05
- Subjects:
- Gastroenterology -- Periodicals
Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
Gastroenterology -- Periodicals
Liver Diseases -- Periodicals
616.33 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1440-1746 ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/loi/jgh ↗ - DOI:
- 10.1111/jgh.12842 ↗
- Languages:
- English
- ISSNs:
- 0815-9319
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4987.615000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3491.xml