A novel association between COMT and BDNF gene polymorphisms and likelihood of symptomatic dysphagia in older people. Issue 9 (14th June 2015)
- Record Type:
- Journal Article
- Title:
- A novel association between COMT and BDNF gene polymorphisms and likelihood of symptomatic dysphagia in older people. Issue 9 (14th June 2015)
- Main Title:
- A novel association between COMT and BDNF gene polymorphisms and likelihood of symptomatic dysphagia in older people
- Authors:
- Nimmons, D.
Pendleton, N.
Payton, A.
Ollier, W.
Horan, M.
Wilkinson, J.
Hamdy, S. - Abstract:
- <abstract abstract-type="main" id="nmo12609-abs-0001"> <title>Abstract</title> <sec id="nmo12609-sec-0001" sec-type="section"> <title>Background</title> <p>Catechol‐O‐methyl transferase (COMT) and brain‐derived neurotrophic factor (BDNF) are neuro‐modulatory proteins that have been demonstrated to affect cortical plasticity, which in turn has been shown to affect age‐related changes and neuronal functioning in humans. Here, we tested the hypothesis that single nucleotide polymorphisms (SNP) within COMT and BDNF genes are associated with dysphagia in older adults.</p> </sec> <sec id="nmo12609-sec-0002" sec-type="section"> <title>Methods</title> <p>A total of 800 community‐dwelling older individuals were sent the Sydney Oropharyngeal Dysphagia Questionnaire to identify swallowing difficulties. DNA from this population was available for study and used to genotype 18 COMT and 12 BDNF polymorphisms. Logistic regression statistical models were used to identify potential associations between dysphagia and the genotypes.</p> </sec> <sec id="nmo12609-sec-0003" sec-type="section"> <title>Key Results</title> <p>A total of 638 individuals completed the questionnaire, giving an 80% response rate. Of these, 538 were genotyped for COMT and BDNF polymorphisms. Age was found to predict dysphagia (<italic>p</italic> = 0.018, OR = 1.08, CI = 1.01–1.14). The COMT polymorphism <italic><bold>rs165599</bold></italic> and the BDNF polymorphism <italic><bold>rs10835211</bold></italic> were found to<abstract abstract-type="main" id="nmo12609-abs-0001"> <title>Abstract</title> <sec id="nmo12609-sec-0001" sec-type="section"> <title>Background</title> <p>Catechol‐O‐methyl transferase (COMT) and brain‐derived neurotrophic factor (BDNF) are neuro‐modulatory proteins that have been demonstrated to affect cortical plasticity, which in turn has been shown to affect age‐related changes and neuronal functioning in humans. Here, we tested the hypothesis that single nucleotide polymorphisms (SNP) within COMT and BDNF genes are associated with dysphagia in older adults.</p> </sec> <sec id="nmo12609-sec-0002" sec-type="section"> <title>Methods</title> <p>A total of 800 community‐dwelling older individuals were sent the Sydney Oropharyngeal Dysphagia Questionnaire to identify swallowing difficulties. DNA from this population was available for study and used to genotype 18 COMT and 12 BDNF polymorphisms. Logistic regression statistical models were used to identify potential associations between dysphagia and the genotypes.</p> </sec> <sec id="nmo12609-sec-0003" sec-type="section"> <title>Key Results</title> <p>A total of 638 individuals completed the questionnaire, giving an 80% response rate. Of these, 538 were genotyped for COMT and BDNF polymorphisms. Age was found to predict dysphagia (<italic>p</italic> = 0.018, OR = 1.08, CI = 1.01–1.14). The COMT polymorphism <italic><bold>rs165599</bold></italic> and the BDNF polymorphism <italic><bold>rs10835211</bold></italic> were found to predict dysphagia and have an interactive effect (<italic>p</italic> = 0.028), which varied according to the carrier status of the other. In the case of SNP <italic><bold>rs10835211</bold></italic>, the effect of heterozygosity was protective or harmful dependent on the respective status of <italic><bold>rs165599</bold></italic>.</p> </sec> <sec id="nmo12609-sec-0004" sec-type="section"> <title>Conclusions &amp; Inferences</title> <p>These results suggest that certain interactions between plasticity genes contribute to the development of dysphagia with increasing age. This highlights a possible role for genetic factors in future monitoring and treating individuals affected by dysphagia.</p> </sec> </abstract> … (more)
- Is Part Of:
- Neurogastroenterology & motility. Volume 27:Issue 9(2015:Sep.)
- Journal:
- Neurogastroenterology & motility
- Issue:
- Volume 27:Issue 9(2015:Sep.)
- Issue Display:
- Volume 27, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 27
- Issue:
- 9
- Issue Sort Value:
- 2015-0027-0009-0000
- Page Start:
- 1223
- Page End:
- 1231
- Publication Date:
- 2015-06-14
- Subjects:
- Gastrointestinal system -- Motility -- Periodicals
Gastrointestinal system -- Innervation -- Periodicals
616.33 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=nmo ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2982 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/nmo.12609 ↗
- Languages:
- English
- ISSNs:
- 1350-1925
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.371450
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3768.xml