Emotion recognition in Huntington's disease: a systematic review
Susie M D Henley1, Marianne J U Novak, Chris Frost
1Research Department of Clinical, Educational and Health Psychology, University College London, London WC1E 6BT, UK. Susie.Henley@ucl.ac.uk
Neuroscience and Biobehavioral Reviews
|June 25, 2011
Summary
Huntington
Area of Science:
- Neuroscience
- Psychology
- Genetics
Background:
- Huntington's disease (HD) is a neurodegenerative disorder.
- Emotion recognition deficits are a known symptom of HD.
- Previous research shows conflicting results regarding specific emotion recognition impairments.
Purpose of the Study:
- To systematically review and synthesize existing literature on emotion recognition in Huntington's disease.
- To clarify the nature and extent of emotion recognition deficits in both manifest and premanifest HD.
- To identify patterns and inconsistencies in emotion recognition across different emotions and modalities.
Main Methods:
- A systematic review and narrative synthesis approach was employed.
- Searches were conducted across Embase, MEDLINE, PsychINFO, and Pubmed databases (1993-2010).
- Included studies investigating emotion recognition in individuals with HD.
Main Results:
- Manifest HD consistently shows impaired recognition of facial expressions of anger.
- Recognition of all negative emotions (facial and vocal) tends to be impaired in manifest HD.
- Impairments in premanifest HD are inconsistent but observed for facial expressions of negative emotions.
Conclusions:
- Evidence suggests a general impairment in recognizing negative emotions in Huntington's disease, especially facial expressions.
- Inconsistencies in findings may stem from HD's inherent variability or methodological differences between studies.
- Future research should utilize more ecologically valid tests and examine inter-modality differences in emotion recognition.
Related Concept Videos
Huntington Disease l: Introduction
Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show reduced penetrance,...
Neural Regulation
Digestion begins with a cephalic phase that prepares the digestive system to receive food. When our brain processes visual or olfactory information about food, it triggers impulses in the cranial nerves innervating the salivary glands and stomach to prepare for food.
Alzheimer Disease l: Introduction
Alzheimer disease is a chronic, progressive, and irreversible neurodegenerative disorder and the most common cause of dementia in older adults. It leads to gradual neuronal loss, causing cognitive decline, behavioral changes, and loss of functional independence.Risk Factors and EtiologyThe disease is multifactorial. Age is the strongest risk factor, with prevalence doubling every 5 years after age 65. Genetic factors include mutations in genes such as APP, PSEN1, and PSEN2, which are associated...

