TY - JOUR
T1 - Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study
AU - The REGISTRY investigators of the European Huntington's Disease Network
AU - McNulty, Paul
AU - Pilcher, Richard
AU - Ramesh, Raviram
AU - Necuiniate, Renata
AU - Hughes, Alis
AU - Farewell, Daniel
AU - Holmans, Peter
AU - Jones, Lesley
AU - Bonelli, Raphael M.
AU - Hecht, Karen
AU - Herranhof, Brigitte
AU - Holl, Anna
AU - Kapfhammer, Hans Peter
AU - Koppitz, Michael
AU - Lilek, Sabine
AU - Magnet, Markus
AU - Müller, Nicole
AU - Otti, Daniela
AU - Painold, Annamaria
AU - Reisinger, Karin
AU - Scheibl, Monika
AU - Schöggl, Helmut
AU - Ullah, Jasmin
AU - Braunwarth, Eva Maria
AU - Brugger, Florian
AU - Buratti, Lisa
AU - Hametner, Eva Maria
AU - Hepperger, Caroline
AU - Holas, Christiane
AU - Hotter, Anna
AU - Hussl, Anna
AU - Larcher, Barbara
AU - Mahlknecht, Philipp
AU - Müller, Christoph
AU - Pinter, Bernadette
AU - Poewe, Werner
AU - Reiter, Eva Magdalena
AU - Seppi, Klaus
AU - Sprenger, Fabienne
AU - Wenning, Gregor
AU - Ladurner, Gunther
AU - Lilek, Stefan
AU - Sinadinosa, Daniela
AU - Staffen, Wolfgang
AU - Walleczek, Anna Maria
AU - Constant, Eric
AU - Reetz, Kathrin
AU - Capetian, Philipp
AU - Goerendt, Ines
AU - Münchau, Alexander
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Background: People with Huntington's disease (HD) have been observed to have lower rates of cancers. Objective: To investigate the relationship between age of onset of HD, CAG repeat length, and cancer diagnosis. Methods: Data were obtained from the European Huntington's disease network REGISTRY study for 6540 subjects. Population cancer incidence was ascertained from the GLOBOCAN database to obtain standardised incidence ratios of cancers in the REGISTRY subjects. Results: 173/6528 HD REGISTRY subjects had had a cancer diagnosis. The age-standardised incidence rate of all cancers in the REGISTRY HD population was 0.26 (CI 0.22-0.30). Individual cancers showed a lower age-standardised incidence rate compared with the control population with prostate and colorectal cancers showing the lowest rates. There was no effect of CAG length on the likelihood of cancer, but a cancer diagnosis within the last year was associated with a greatly increased rate of HD onset (Hazard Ratio 18.94, p < 0.001). Conclusions: Cancer is less common than expected in the HD population, confirming previous reports. However, this does not appear to be related to CAG length in HTT. A recent diagnosis of cancer increases the risk of HD onset at any age, likely due to increased investigation following a cancer diagnosis.
AB - Background: People with Huntington's disease (HD) have been observed to have lower rates of cancers. Objective: To investigate the relationship between age of onset of HD, CAG repeat length, and cancer diagnosis. Methods: Data were obtained from the European Huntington's disease network REGISTRY study for 6540 subjects. Population cancer incidence was ascertained from the GLOBOCAN database to obtain standardised incidence ratios of cancers in the REGISTRY subjects. Results: 173/6528 HD REGISTRY subjects had had a cancer diagnosis. The age-standardised incidence rate of all cancers in the REGISTRY HD population was 0.26 (CI 0.22-0.30). Individual cancers showed a lower age-standardised incidence rate compared with the control population with prostate and colorectal cancers showing the lowest rates. There was no effect of CAG length on the likelihood of cancer, but a cancer diagnosis within the last year was associated with a greatly increased rate of HD onset (Hazard Ratio 18.94, p < 0.001). Conclusions: Cancer is less common than expected in the HD population, confirming previous reports. However, this does not appear to be related to CAG length in HTT. A recent diagnosis of cancer increases the risk of HD onset at any age, likely due to increased investigation following a cancer diagnosis.
UR - http://www.scopus.com/inward/record.url?scp=85051366290&partnerID=8YFLogxK
U2 - 10.3233/JHD-170263
DO - 10.3233/JHD-170263
M3 - Journal articles
C2 - 30103338
AN - SCOPUS:85051366290
SN - 1879-6397
VL - 7
SP - 209
EP - 222
JO - Journal of Huntington's Disease
JF - Journal of Huntington's Disease
IS - 3
ER -