Cargando…
Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls
BACKGROUND: Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly for patients over 60ys. We hypothesised that indiv...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891994/ https://www.ncbi.nlm.nih.gov/pubmed/24354965 http://dx.doi.org/10.1186/1750-1172-8-195 |
_version_ | 1782299441034690560 |
---|---|
author | Hosman, Anna E Devlin, Hannah L Silva, B Maneesha Shovlin, Claire L |
author_facet | Hosman, Anna E Devlin, Hannah L Silva, B Maneesha Shovlin, Claire L |
author_sort | Hosman, Anna E |
collection | PubMed |
description | BACKGROUND: Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly for patients over 60ys. We hypothesised that individuals with HHT may be protected against life-limiting cancers. METHODS: To compare specific cancer rates in HHT patients and controls, we developed a questionnaire capturing data on multiple relatives per respondent, powered to detect differences in the four most common solid non skin cancers (breast, colorectal, lung and prostate), each associated with significant mortality. Blinded to cancer responses, reports of HHT-specific features allowed assignment of participants and relatives as HHT-subjects, unknowns, or controls. Logistic and quadratic regressions were used to compare rates of specific cancer types between HHT subjects and controls. RESULTS: 1,307 participants completed the questionnaire including 1,007 HHT-subjects and 142 controls. The rigorous HHT diagnostic algorithm meant that 158 (12%) completed datasets were not assignable either to HHT or control status. For cancers predominantly recognised as primary cancers, the rates in the controls generally matched age-standardised rates for the general population. HHT subjects recruited through the survey had similar demographics to controls, although the HHT group reported a significantly greater smoking habit. Combining data of participants and uniquely-reported relatives resulted in an HHT-arm of 2,161 (58% female), and control-arm of 2,817 (52% female), with median ages of 66ys [IQR 53–77] and 77ys [IQR 65–82] respectively. In both crude and age-adjusted regression, lung cancers were significantly less frequent in the HHT arm than controls (age-adjusted odds ratio 0.48 [0.30, 0.70], p = 0.0012). Breast cancer prevalence was higher in HHT than controls (age-adjusted OR 1.52 [1.07, 2.14], p = 0.018). Overall, prostate and colorectal cancer rates were equivalent, but the pattern of colorectal cancer was modified, with a higher prevalence in younger HHT patients than controls. CONCLUSIONS: These preliminary survey data suggest clinically significant differences in the rates of lung, breast and colorectal cancer in HHT patients compared to controls. For rare diseases in which longitudinal studies take decades to recruit equivalent datasets, this type of methodology provides a good first-step method for data collection. |
format | Online Article Text |
id | pubmed-3891994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38919942014-01-15 Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls Hosman, Anna E Devlin, Hannah L Silva, B Maneesha Shovlin, Claire L Orphanet J Rare Dis Research BACKGROUND: Hereditary haemorrhagic telangiectasia (HHT) is inherited as an autosomal dominant trait, affects ~1 in 5,000, and causes multi-systemic vascular lesions and life-limiting complications. Life expectancy is surprisingly good, particularly for patients over 60ys. We hypothesised that individuals with HHT may be protected against life-limiting cancers. METHODS: To compare specific cancer rates in HHT patients and controls, we developed a questionnaire capturing data on multiple relatives per respondent, powered to detect differences in the four most common solid non skin cancers (breast, colorectal, lung and prostate), each associated with significant mortality. Blinded to cancer responses, reports of HHT-specific features allowed assignment of participants and relatives as HHT-subjects, unknowns, or controls. Logistic and quadratic regressions were used to compare rates of specific cancer types between HHT subjects and controls. RESULTS: 1,307 participants completed the questionnaire including 1,007 HHT-subjects and 142 controls. The rigorous HHT diagnostic algorithm meant that 158 (12%) completed datasets were not assignable either to HHT or control status. For cancers predominantly recognised as primary cancers, the rates in the controls generally matched age-standardised rates for the general population. HHT subjects recruited through the survey had similar demographics to controls, although the HHT group reported a significantly greater smoking habit. Combining data of participants and uniquely-reported relatives resulted in an HHT-arm of 2,161 (58% female), and control-arm of 2,817 (52% female), with median ages of 66ys [IQR 53–77] and 77ys [IQR 65–82] respectively. In both crude and age-adjusted regression, lung cancers were significantly less frequent in the HHT arm than controls (age-adjusted odds ratio 0.48 [0.30, 0.70], p = 0.0012). Breast cancer prevalence was higher in HHT than controls (age-adjusted OR 1.52 [1.07, 2.14], p = 0.018). Overall, prostate and colorectal cancer rates were equivalent, but the pattern of colorectal cancer was modified, with a higher prevalence in younger HHT patients than controls. CONCLUSIONS: These preliminary survey data suggest clinically significant differences in the rates of lung, breast and colorectal cancer in HHT patients compared to controls. For rare diseases in which longitudinal studies take decades to recruit equivalent datasets, this type of methodology provides a good first-step method for data collection. BioMed Central 2013-12-20 /pmc/articles/PMC3891994/ /pubmed/24354965 http://dx.doi.org/10.1186/1750-1172-8-195 Text en Copyright © 2013 Hosman 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hosman, Anna E Devlin, Hannah L Silva, B Maneesha Shovlin, Claire L Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title | Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title_full | Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title_fullStr | Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title_full_unstemmed | Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title_short | Specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
title_sort | specific cancer rates may differ in patients with hereditary haemorrhagic telangiectasia compared to controls |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3891994/ https://www.ncbi.nlm.nih.gov/pubmed/24354965 http://dx.doi.org/10.1186/1750-1172-8-195 |
work_keys_str_mv | AT hosmanannae specificcancerratesmaydifferinpatientswithhereditaryhaemorrhagictelangiectasiacomparedtocontrols AT devlinhannahl specificcancerratesmaydifferinpatientswithhereditaryhaemorrhagictelangiectasiacomparedtocontrols AT silvabmaneesha specificcancerratesmaydifferinpatientswithhereditaryhaemorrhagictelangiectasiacomparedtocontrols AT shovlinclairel specificcancerratesmaydifferinpatientswithhereditaryhaemorrhagictelangiectasiacomparedtocontrols |