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CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY
BACKGROUND: The aetiology of juvenile idiopathic arthritis (JIA) is largely unknown. We have established a JIA biobank in Melbourne, Australia called CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY, with the broad aim of identifying genomic and environmental disease risk factors. We p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551677/ https://www.ncbi.nlm.nih.gov/pubmed/23153063 http://dx.doi.org/10.1186/1546-0096-10-37 |
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author | Ellis, Justine A Ponsonby, Anne-Louise Pezic, Angela Chavez, Raul A Allen, Roger C Akikusa, Jonathan D Munro, Jane E |
author_facet | Ellis, Justine A Ponsonby, Anne-Louise Pezic, Angela Chavez, Raul A Allen, Roger C Akikusa, Jonathan D Munro, Jane E |
author_sort | Ellis, Justine A |
collection | PubMed |
description | BACKGROUND: The aetiology of juvenile idiopathic arthritis (JIA) is largely unknown. We have established a JIA biobank in Melbourne, Australia called CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY, with the broad aim of identifying genomic and environmental disease risk factors. We present here study protocols, and a comparison of socio-demographic, pregnancy, birth and early life characteristics of cases and controls collected over the first 3 years of the study. METHODS: Cases are children aged ≤18 years with a diagnosis of JIA by 16 years. Controls are healthy children aged ≤18 years, born in the state of Victoria, undergoing a minor elective surgical procedure. Participant families provide clinical, epidemiological and environmental data via questionnaire, and a blood sample is collected. RESULTS: Clinical characteristics of cases (n = 262) are similar to those previously reported. Demographically, cases were from families of higher socio-economic status. After taking this into account, the residual pregnancy and perinatal profiles of cases were similar to control children. No case-control differences in breastfeeding commencement or duration were detected, nor was there evidence of increased case exposure to tobacco smoke in utero. At interview, cases were less likely to be exposed to active parental smoking, but disease-related changes to parent behaviour may partly underlie this. CONCLUSIONS: We show that, after taking into account socio-economic status, CLARITY cases and controls are well matched on basic epidemiological characteristics. CLARITY represents a new study platform with which to generate new knowledge as to the environmental and biological risk factors for JIA. |
format | Online Article Text |
id | pubmed-3551677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35516772013-01-24 CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY Ellis, Justine A Ponsonby, Anne-Louise Pezic, Angela Chavez, Raul A Allen, Roger C Akikusa, Jonathan D Munro, Jane E Pediatr Rheumatol Online J Research BACKGROUND: The aetiology of juvenile idiopathic arthritis (JIA) is largely unknown. We have established a JIA biobank in Melbourne, Australia called CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY, with the broad aim of identifying genomic and environmental disease risk factors. We present here study protocols, and a comparison of socio-demographic, pregnancy, birth and early life characteristics of cases and controls collected over the first 3 years of the study. METHODS: Cases are children aged ≤18 years with a diagnosis of JIA by 16 years. Controls are healthy children aged ≤18 years, born in the state of Victoria, undergoing a minor elective surgical procedure. Participant families provide clinical, epidemiological and environmental data via questionnaire, and a blood sample is collected. RESULTS: Clinical characteristics of cases (n = 262) are similar to those previously reported. Demographically, cases were from families of higher socio-economic status. After taking this into account, the residual pregnancy and perinatal profiles of cases were similar to control children. No case-control differences in breastfeeding commencement or duration were detected, nor was there evidence of increased case exposure to tobacco smoke in utero. At interview, cases were less likely to be exposed to active parental smoking, but disease-related changes to parent behaviour may partly underlie this. CONCLUSIONS: We show that, after taking into account socio-economic status, CLARITY cases and controls are well matched on basic epidemiological characteristics. CLARITY represents a new study platform with which to generate new knowledge as to the environmental and biological risk factors for JIA. BioMed Central 2012-11-15 /pmc/articles/PMC3551677/ /pubmed/23153063 http://dx.doi.org/10.1186/1546-0096-10-37 Text en Copyright ©2012 Ellis et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ellis, Justine A Ponsonby, Anne-Louise Pezic, Angela Chavez, Raul A Allen, Roger C Akikusa, Jonathan D Munro, Jane E CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title | CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title_full | CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title_fullStr | CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title_full_unstemmed | CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title_short | CLARITY – ChiLdhood Arthritis Risk factor Identification sTudY |
title_sort | clarity – childhood arthritis risk factor identification study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551677/ https://www.ncbi.nlm.nih.gov/pubmed/23153063 http://dx.doi.org/10.1186/1546-0096-10-37 |
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