Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/176
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dc.contributor.authorKarunanayake, A.
dc.contributor.authorRajindrajith, S.en
dc.contributor.authorDevanarayana, N.M.en
dc.date.accessioned2017-07-12T09:36:43Z
dc.date.available2017-07-12T09:36:43Z
dc.date.issued2017
dc.identifier.citationANMA & JSNM Joint Meeting, Osaka International Convention Center (OICC) Japanen_US
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/176
dc.descriptionAbstract, 5th Biennial Congress of the Asian Neurogastroenterology and Motility Association,& 19th Annual Meeting of Japanese Society of Neurogastroenterology and Motility, March 23-25, 2017, Osaka, Japanen_US
dc.description.abstractINTRODUCTION The pathophysiology of AP-FGIDs in children are poorly understood. Animal and human studies have suggested that adverse ELE such as pain or stress can induce long-term changes in the neurons. Apart from the abuse other aspects in early life have not been well investigated. METHODS ELE were evaluated in 182 school children with AP-FGIDs (62.1% girls, mean age 8.5, SD 2.1) and 571 children without AP-FGIDs recruited as controls (51.1% girls, mean age 8.8 SD 1.9 ) using a translated and pretested parental questionnaire. AP- FGIDs were diagnosed by Rome III criteria. RESULTS Compared to controls AP-FGIDs patients were low in birth order (1.7 vs. 1.9 p=0.01). Birth order of the parents, maternal and paternal age of marriage and number of members in the house were not associated with AP-FGIDs (p >0.05, Independent sample T test.). Prenatal complications (14.8% vs. 7.4% p= 0.002) and post-natal complications and receiving PBU care (7.7% vs. 3.1% p=0.008) were significantly higher in AP-FGIDs. Gestational period, mode of delivery, duration of hospital stay, period of exclusive breast feeding and duration of breast feeding were not significantly different (p>0.05). Presence of a family member with abdominal pain lasting more than 2 months and the presence of a family member with chronic pain (other than abdominal pain) in the family is also significantly higher in AP-FGIDs families (p<0.0001, Chi-square test). CONCLUSION ELEs occurring during pre and post-natal periods, which is a vulnerable period for developing neurons may be an important contributory factor for the development of AP-FGIDs. Familial predisposition for development of AP-FGIDs highlight the possible genetic basis for pathogenesis of AP-FGIDs. Breast feeding does not protective against the development of AP-FGIDs.en_US
dc.language.isoen_USen_US
dc.publisherJapanese Society of Neurogastroenterology and Motility (JSNM), Asian Neurogastroenterology and Motility Association(ANMA)en_US
dc.subjectGastrointestinal Disordersen_US
dc.titleImpact of early life events (ELE) and family dynamics for developments of abdominal pain predominate functional gastrointestinal disorders (AP-FGIDs) in 5-12 age groupen_US
dc.typeConference Abstracten_US
Appears in Collections:Conference Papers

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