Literature DB >> 1479606

Causes of death in patients with Huntington's disease and in unaffected first degree relatives.

S A Sørensen1, K Fenger.   

Abstract

Causes of death were examined from death certificates for 395 Danish subjects with Huntington's disease (HD) and for 282 unaffected sibs and compared with the causes of death in the general Danish population. For both the HD subjects and the sibs, pneumonia and cardiovascular diseases were the most frequent primary causes of death. Suicides accounted for 5.6% of all deaths among the HD subjects and, unexpectedly, for 5.3% among the sibs, some of whom may have been carriers of the HD gene. Both were significantly higher than the corresponding frequency of 2.7% in the general Danish population, but there was no evidence of differences in the age specific proportions for the HD subjects and for the sibs compared to the general population. Some accidents leading to death in the sibs may have been hidden suicides. The rate of cancer was low for the HD patients, being only 5.3% compared with 31.2% for the sibs. Neurological diseases were reported with an increased frequency in the HD patients compared to the general population, 6% v 1%.

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Year:  1992        PMID: 1479606      PMCID: PMC1016212          DOI: 10.1136/jmg.29.12.911

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  9 in total

1.  [Length of illness and life expectancy in Huntington's chorea].

Authors:  G G WENDT; I LANDZETTEL; K SOLTH
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1960

2.  Huntington's chorea in Michigan. I. Demography and genetics.

Authors:  T E REED; J H CHANDLER
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

3.  Conditions associated with Huntington's disease at death. A case-control study.

Authors:  D J Lanska; M J Lanska; L Lavine; B S Schoenberg
Journal:  Arch Neurol       Date:  1988-08

4.  Causes of death in Huntington's disease.

Authors:  E Chiu; L Alexander
Journal:  Med J Aust       Date:  1982-02-20       Impact factor: 7.738

5.  Social perspectives in Huntington's chorea.

Authors:  M R Hayden; R Ehrlich; H Parker; S J Ferera
Journal:  S Afr Med J       Date:  1980-08-02

Review 6.  Huntington disease: genetics and epidemiology.

Authors:  P M Conneally
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

7.  Increased rate of suicide among patients with Huntington's disease.

Authors:  M Schoenfeld; R H Myers; L A Cupples; B Berkman; D S Sax; E Clark
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-12       Impact factor: 10.154

8.  Causes of death in Huntington disease as reported on death certificates.

Authors:  J L Haines; P M Conneally
Journal:  Genet Epidemiol       Date:  1986       Impact factor: 2.135

9.  Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk.

Authors:  L A Farrer
Journal:  Am J Med Genet       Date:  1986-06
  9 in total
  56 in total

1.  A Case of Previously Unsuspected Huntington Disease Diagnosed at Autopsy.

Authors:  Catherine R Miller; Nobby C Mambo; Jianli Dong; Gerald A Campbell
Journal:  Acad Forensic Pathol       Date:  2017-03-01

Review 2.  Shaping the role of mitochondria in the pathogenesis of Huntington's disease.

Authors:  Veronica Costa; Luca Scorrano
Journal:  EMBO J       Date:  2012-03-23       Impact factor: 11.598

3.  Aberrant heart rate and brainstem brain-derived neurotrophic factor (BDNF) signaling in a mouse model of Huntington's disease.

Authors:  Kathleen J Griffioen; Ruiqian Wan; Tashalee R Brown; Eitan Okun; Simonetta Camandola; Mohamed R Mughal; Terry M Phillips; Mark P Mattson
Journal:  Neurobiol Aging       Date:  2011-12-31       Impact factor: 4.673

4.  A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease.

Authors:  E W Almqvist; M Bloch; R Brinkman; D Craufurd; M R Hayden
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

5.  Drp1/Fis1-mediated mitochondrial fragmentation leads to lysosomal dysfunction in cardiac models of Huntington's disease.

Authors:  A U Joshi; A E Ebert; B Haileselassie; D Mochly-Rosen
Journal:  J Mol Cell Cardiol       Date:  2018-12-11       Impact factor: 5.000

Review 6.  Therapeutic perspectives for the treatment of Huntington's disease: treating the whole body.

Authors:  Bronwen Martin; Erin Golden; Alex Keselman; Matthew Stone; Mark P Mattson; Josephine M Egan; Stuart Maudsley
Journal:  Histol Histopathol       Date:  2008-02       Impact factor: 2.303

7.  Upper gastrointestinal findings in Huntington's disease: patients suffer but do not complain.

Authors:  Jürgen E Andrich; Michael Wobben; Peter Klotz; Oliver Goetze; Carsten Saft
Journal:  J Neural Transm (Vienna)       Date:  2009-09-22       Impact factor: 3.575

8.  Huntingtin N17 domain is a reactive oxygen species sensor regulating huntingtin phosphorylation and localization.

Authors:  Laura F DiGiovanni; Andrew J Mocle; Jianrun Xia; Ray Truant
Journal:  Hum Mol Genet       Date:  2016-07-27       Impact factor: 6.150

Review 9.  Therapeutic approaches to preventing cell death in Huntington disease.

Authors:  Anna Kaplan; Brent R Stockwell
Journal:  Prog Neurobiol       Date:  2012-08-28       Impact factor: 11.685

10.  Formation of polyglutamine inclusions in a wide range of non-CNS tissues in the HdhQ150 knock-in mouse model of Huntington's disease.

Authors:  Hilary Moffitt; Graham D McPhail; Ben Woodman; Carl Hobbs; Gillian P Bates
Journal:  PLoS One       Date:  2009-11-30       Impact factor: 3.240

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