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16 June 2017

Neuropsychiatric Burden in Huntington’s Disease

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1
Department of Psychiatry, Università degli Studi di Milano, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan 20122, Italy
2
Department of Neuro-Oncology, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan 20133, Italy
3
Department of Neurology-Stroke Unit and Laboratory of Neuroscience, IRCCS Istituto Auxologico Italiano, Milan 20149, Italy
4
Department of Pathophysiology and Transplantation, “Dino Ferrari” Center, Università degli Studi di Milano, Milan 20122, Italy
Brain Sci.2017, 7(6), 67;https://doi.org/10.3390/brainsci7060067
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Abstract

Huntington’s disease is a disorder that results in motor, cognitive, and psychiatric problems. The symptoms often take different forms and the presence of disturbances of the psychic sphere reduces patients’ autonomy and quality of life, also impacting patients’ social life. It is estimated that a prevalence between 33% and 76% of the main psychiatric syndromes may arise in different phases of the disease, often in atypical form, even 20 years before the onset of chorea and dementia. We present a narrative review of the literature describing the main psychopathological patterns that may be found in Huntington’s disease, searching for a related article in the main database sources (Medline, ISI Web of Knowledge, Scopus, and Medscape). Psychiatric conditions were classified into two main categories: affective and nonaffective disorders/symptoms; and anxiety and neuropsychiatric features such as apathy and irritability. Though the literature is extensive, it is not always convergent, probably due to the high heterogeneity of methods used. We summarize main papers for pathology and sample size, in order to present a synoptic vision of the argument. Since the association between Huntington’s disease and psychiatric symptoms was demonstrated, we argue that the prevalent and more invalidating psychiatric components should be recognized as early as possible during the disease course in order to best address psychopharmacological therapy, improve quality of life, and also reduce burden on caregivers.

1. Introduction

Huntington’s disease (HD) is a neurodegenerative disease inherited in an autosomal dominant fashion, characterized by progressive movement disorders associated with cognitive and psychiatric symptoms [1,2]. The first clinical picture of the illness was provided in 1842 by Waters. Not until 1872 did George Huntington name the disease Huntington’s chorea, after a complete description of the symptoms and clinical course. By the 1980s, the name of the disease became known as Huntington’s disease, with the recognition of its motor and non-motor signs and symptoms [3]. Following the introduction of molecular biology techniques, a linkage was found on chromosome 4 in 1983, and 10 years later the gene for HD was discovered [2]. The underlying genetic defect is an unstable CAG trinucleotide repeat expansion in exon 1 of the HD gene, formerly called IT-15, on the short arm of chromosome 4. A repeat CAG length of 36 and longer is pathogenic and results in the synthesis of an abnormal polyglutamic tract in Huntington’s, a widely expressed protein of uncertain function [4,5] causing accumulation of intracellular protein aggregates, neurotrophic factor deprivation, impairment of energetic metabolism, transcriptional deregulation and, finally, hyperactivation of programmed cell-death mechanisms. Progressive dysfunction and neuronal loss, mainly in the caudate nucleus and in the putamen, start several years before the onset of motor symptoms. Along with basal ganglia pathology, neurodegeneration occurs in a large cortical region, in the thalamus, hypothalamus, and cerebellum [6,7].
Dopamine, glutamate, and γ-aminobutyric acid are thought to be the most affected neurotransmitters in HD and are currently the focus of pharmacotherapy [8]. The age of HD onset is inversely correlated with the length of the expansion in people with 40 or more CAG repeats, who will inevitably manifest the disease if they live a normal lifespan. In fact, when a number of CAG repeats between 36 and 39 presents, the penetrance is variable. In addition, it has been suggested that there may be subtle abnormalities, possibly constituting an endophenotype, in the rare individuals who have repeat lengths in the 27–35 range [1,2,6]. A recent systematic review by Wexler et al. [9] estimated a general incidence rate of 7.2 million people/years.
A meta-regression made by Pringssheim et al. [10] confirmed a significantly lower prevalence of HD in Asia compared to Europe, North America, and Australia. In particular, recent studies in a different part of the world reported that the prevalence should be updated with respect to older studies before the advent of the molecular diagnosis of Huntington disease (HTT) studies. For instance, Fisher et al [11] reported a prevalence in Canada of 17.2 in the Caucasian population per 100.00 and of 13.7 per 100.000 in the general population, while an Italian study reported a prevalence of 10.85 per 100.000 [12]. A lower prevalence is registered in Japan [13,14].
In most cases, the age of onset of HD is between 35 and 45 years, whereas the mean duration of the disease is 16 years [15,16]. Different stages of the disease may be described (premanifest, with soft signs, phenoconversion, and manifest), each being characterized by decreasing independence and the need for help caused by a deterioration of motor and cognitive performance and the presence of psychiatric symptoms [13].
Currently, symptomatic treatment is available for motor and psychiatric symptoms, but there is still no evidence that therapy can slow the evolution of brain degeneration.

2. Methods

Searches were conducted through Medline, ISI Web of Knowledge, Scopus, and Medscape. The following keywords or combinations were used: “apathy”, “behavioral”, “depression”, “irritability”, “neuropsychiatric symptoms”, “psychiatric”, “psychotic”, “sexuality”, and “suicidal”. We did not consider other terms that might impact psychiatric manifestations such as sleep, aggression, and impulsive, in order to focus the search on the main psychiatric symptoms. In so doing, some studies about specific psychiatric manifestations might have been excluded.
A total of 3055 papers were initially identified. A screening of the articles’ abstracts was then performed in order to consider only those articles that concerned with the topic of the review and removing duplicates.
Additional papers were identified during the reading (also during the revision process) and analyzed to be assessed as a potential data source.
The initial search identified 3055 articles. One thousand eight hundred and twenty-nine papers matched with term “psychiatric”, 495 “depression”, 137 “psychotic”, 43 “suicidal”, 35 “sexuality”, 62 “apathy”, 245 “behavioral”, 135 “neuropsychiatric symptoms”, and 74 “irritability”. An initial review of the titles and abstracts of these articles by three of the authors identified 238 articles that were potentially relevant to the current review. The abstracts of these articles were then evaluated against the inclusion criteria by the authors, resulting in 82 articles being identified as eligible for inclusion, with an additional six articles identified during manuscript preparation, for a total of 88 articles. This review provides a narrative synthesis of the findings from previous key reviews and empirical studies identified in the literature search.
Inclusion and exclusion criteria:
We included articles assessing the prevalence, incidence, and phenomenology of neuropsychiatric and psychiatric symptoms in patients with HD. We included only articles reporting data about patients with a genetic diagnosis. This suggested a lower time limit to the search that started from 1983. We also included articles reporting data about the preclinical presentation of psychiatric and neuropsychiatric symptoms. We didn’t posit limits to the sample size of the studies considered.
We excluded reviews, editorials, opinion papers, letters, surveys, and articles not clearly reporting the methodology used, the sample size, and/or not written in English.

3. Clinical Features in HD and Psychiatric Disorders

Clinical pictures of HD comprise motor abnormalities (chorea, dystonia, bradykinesia, oculomotor dysfunction), cognitive impairment, behavioral problems, and psychiatric disorders. The latter are major constituents of the clinical spectrum of HD and have a substantial impact on daily functioning, constituting the most distressing aspect (for both patient and relatives) and often the reason for hospitalization [17,18]. In the early descriptions of HD, more attention was given to its cognitive features and dementia. Starting in the literature published in the 1990s, many facets of HD have been described including specific psychiatric aspects. Behavioral and psychiatric symptoms (also called prodromal) often precede the manifestation of motor abnormalities of HD [19]. Historical description estimated rates for lifetime prevalence of psychiatric disorders among HD patients vary widely between 33% and 76% [20,21].
Several recent studies have described neuropsychiatric symptoms including depressed mood, mania, irritability, anxiety, apathy, obsessions-compulsions, and psychosis. Prevalence variation depends on the different methods used to detect and evaluate (e.g., interview, rating scales, self-report questionnaires) (Table 1) [1,22,23,24,25].
Table 1. Neuropsychiatric disturbances in mutation carriers.
This result contrasts with incidence rates found in other neurodegenerative diseases (e.g., Parkinson’s disease, in which an incidence rate of major depressive disorder (MDD) of 2% per year is reported) [26,27]. Furthermore, switching to a different psychiatric disorder is not rare. Many factors, including rigid diagnostic criteria, presence of physical symptoms, cognitive impairment, and patient medical history collected by informal caregiver interviews are considered confounding factors [22].

3.1. Affective Disorders

The most frequent psychiatric sign occurring in HD patients consists of a depressive symptomatology (DS) [28]. The diagnosis is sometimes difficult because somatic expression of depressed mood (i.e., apathy, inactivity, and weight loss) also occurs in HD patients without psychiatric problems [13]. Estimated prevalence of depression in HD varies widely, ranging from 9% to 63%, with several studies suggesting rates between 40% and 50% (Table 2) [29,30,31,32,33,34,35,36,37,38,39,40]. Kirkwood et al. (2001) suggested that sadness and depression were two of the earliest symptoms at HD onset detected by first-degree relatives’ reports [37].
Table 2. Depression in mutations carriers.
The development of DS in HD could be a direct result of cerebral degeneration, for which several neuropathological mechanisms have been proposed [41,42] linked to an early neuronal loss in the medial caudate, which has connections to limbic structures [43,44,45]. However, depression might equally well be a consequence of other factors, such as a psychological reaction to being at risk for Huntington’s disease, having experienced an insecure and harmful environment, and/or awareness of the disease’s onset. From a physiological point of view, only a few studies investigated the presynaptic dopaminergic function and no data are yet available on associations with affective symptoms [46,47].
Many studies have found that depressive symptoms precede the onset of motor symptoms but no relation between the occurrence of depressive symptoms and disease duration has so far been reported [48,49]. However, depression may negatively correlate to cognitive decline, which is possibly the result of concurrent decreasing illness awareness [38] and worsened cognitive performance. This is an important point because, if recognized, depression may be properly treated with potential positive consequences on emotional, cognitive, and physical well-being [50]. Paulsen et al. analyzed the relationship between depressive symptoms and disease stage [36] and found the highest rates in the first stages of the disease and lower rates in last stages.
Van Duijn et al. [1,29] described depression as a common characteristic of the disease course, that tends to correlate with the proximity to the clinical onset. Depression seems to increase during the disease course but it is not relevant in the last stage. Furthermore, authors reported that depression is not related to CAG length.
However, in an observational study (the PREDICT protocol study), Epping et al. [30] found that the prevalence of symptoms in prodromal HD patients is not different than the general population. Julien et al. [34] suggested that depression in this early phase cannot be attributed to a general psychological condition linked to being at risk, since it occurs only in a fraction of mutation carriers. No gender effect was found to be significant. This is in contrast with data on the general population, but in other neurodegenerative diseases a similar pattern is observed.
Although depression is the most common specific psychiatric diagnosis in HD, a smaller number of patients become manic, displaying elevated or irritable mood, impulsiveness, hyperactivity, decreased need for sleep, and grandiosity. Some authors have estimated an average rate of mania (with variable definitions of “mania”) of 4.8%, and others have found hypomania and manic episodes in up to 10% of HD patients [51]. Particular attention should be paid to suicide risk. In his original description of the disease, George Huntington stated that there was “a tendency to insanity and suicide”. The suicide rate estimate for HD patients is traditionally 4–6 times higher than in the general population. However, recent studies have confirmed the need to distinguish suicide ideation from attempted suicide, as well as considering differently several groups with different characteristics in order not to introduce confounding data. In particular, depressive symptoms, anxiety, and benzodiazepine consumption are considered risk factors (Table 3) [32,35,52,53,54]. A history of suicide attempts and the presence of depression are strongly predictive of suicidal behavior in prodromal HD. Suicide risk increases in individuals who are closer to motor diagnosis [41].
Table 3. Suicidality in mutation carriers.

3.2. Anxiety

Anxiety has often been reported in HD patients, independent of gender (17%–61%), both due to the course of the disease and from the neurodegenerative process itself. There are contrasting data regarding the critical stage for anxiety and depression to arise, with some studies identifying stage 2 as the most critical and others suggesting stages 4–5. Moreover, some studies have reported that the stage of illness in HD patients does not influence anxiety levels, contrary to depression symptoms [56]. As stated above, assuming benzodiazepine seems to be an independent risk factor for suicide (Table 4) [22,23,24,34,36,38,52].
Table 4. Anxiety in mutations carriers.

3.3. Irritability and Aggression

Irritability (Irr) is a common clinical problem in patients with neuropsychiatric disorders. It has been described in HD, traumatic brain injury [57,58], dementias [59], and Parkinson’s disease [60].
Studies have linked irritability and hostility to other aspects of morbidity, including treatment non-adherence [61], suicide attempts [62,63], and violence. While the term “irritability” is widely used in descriptions of patient behavior, but it remains poorly defined. This lack of consensus prompted a definition of Irr, in addition to arguing that irritable mood is separate from other mood disorders such as depression.
Irritation may be defined as a temporary psychological state characterized by impatience, intolerance, and poorly controlled anger. It includes elements of anger, aggression, and reduced impulse control and can occur independently of depression. Prevalence of Irr among HD patients varies between 35% and 73% (Table 5) [23,24,29,38,63,64,65].
Table 5. Irritability in mutation carriers.
Irr without a prior history of similar symptoms occurs in most HD patients and seems to precede motor symptoms in gene carriers [23,66]. Often Irr is described as the first sign of the disease in pre-symptomatic patients with HD [1] but it may occur during all stages of the disease, more frequently in patients whose neurological symptoms have been present for 6 to 11 years [50].
The prevalence of moderate to severe irritability/aggression increased during the disease course [29,67].
Increasing degeneration of the striatum and the orbitofrontal-subcortical circuit contributes to the development of socially inappropriate behaviors that initially may be manifested as subtle irritability and, in late-stage disease, as aggressive behavior [68]. Nevertheless, it is established that some patients may show paradoxical “aggressive” behavior or behavioral disinhibition following benzodiazepine consumption [63]. Taken together, Irr, depression, and anxiety are three salient clinical features of pre-symptomatic HD.

3.4. Obsessivity

The presence of obsessive and compulsive symptoms (OCs) has been previously documented in patients with HD as less common than other psychiatric symptoms [65,69,70,71,72]. However, a study by Marder et al. reported that 22.3% had obsessive and compulsive symptoms at their first clinical visit, suggesting that these symptoms may be more common than previously recognized in this population. This symptom shows an increase with disease progression with a trend similar to the one of depression and anxiety in the end stage of the disease. Anderson et al. reported that patients with severe OCs have higher psychiatric co-morbidity (e.g., depression, aggression, and delusions) and neuropsychological deficits.
OCs prevalence varies from 7% to 50% and this association is not surprising, as dysfunction of cortico-striatal connections is also a characteristic of primary disease [67,73,74]. The prevalence of moderate to severe OCs increased progressively [29]. van Duijn et al. also reported a higher than normal prevalence of OCs in preclinical mutation carriers [1].
Many HD gene-carriers show personality changes with mental inflexibility in early stages, possibly signaling future OCs (Table 6) [23,29,33,38,65,75].
Table 6. OCs in mutation carriers.

3.5. Psychosis

Prevalence of psychotic symptoms (PS), including paranoia and delusional and psychotic states resembling various types of schizophrenia-like psychosis, varies between 3% and 11% [1]. The association of PS with HD is a consequence of a relative hyperdopaminergic state (Table 7) [23,24,29,38,40,48,76,77].
Table 7. Psychosis in mutation carriers.
Until the first half of the twentieth century, HD patients were often misdiagnosed with dementia praecox or schizophrenia. Now, the low prevalence of PS may be explained by the relatively high use of antipsychotics. PS do not have a specific presentation and must be carefully distinguished from non-organic mental diseases. Some of the patients have a peculiar presentation, as reported by some case reports.
A lack of clinical fluctuation course is typical of a delirium state. PS are usually associated with increasing cognitive impairment and tend to become less overt as the disease progresses. They were found to be particularly important in an advanced stage of the disease. Those patients with an early age at onset of HD seem to be at an increased risk of psychoses [71]. A very low prevalence should be explained by a frequently use of neuroleptics [29].

3.6. Apathy and Neuropsychological Deficits

Apathy (AP) has been described both as a symptom (i.e., of mood disorder, altered level of consciousness, or cognitive impairment) and as a syndrome [78,79]. It is defined as a disorder of motivation, with the loss of or diminished goal-directed behavior, cognitive activity, and/or emotion, as well as functional impairments that are attributable to apathy [80,81]. Clinically, it is associated with a decline of daily living activities causing a great burden of disease and distress in caregivers, [82] also after adjusting for the presence of motor and cognitive deficits. Sometimes it is hard to discriminate apathy from depression core symptoms [21]. Prevalence of AP is a common neuropsychiatric feature of HD and varies from 52% to 76% (Table 8) [24,29,38] and, once present, tends to persist or worsen, with highest rate in the late stage of disease [29].
Table 8. Apathy symptoms in mutation carriers.
Damage to anterior cingulate-subcortical circuit structures has in particular been related with motivational disorders, including apathy, which may also be the case in HD [49,82]. AP has also been correlated with other symptoms of HD, particularly with cognitive impairments, including problems with working memory, planning, problem solving, and executive function deficits [83].
Psychomotor abilities (e.g., hand-eye coordination tasks such as throwing a ball or typing) are significantly impaired, showing a consistent decline across disease progression, while difficulties in visuospatial and memory abilities occur later in HD [82]. In patients with dementia and apathy, a faster cognitive and functional decline has been found compared to patients without apathy. One final example of frontal behaviors that might be relevant in HD is decreased awareness or loss of insight. Although anecdotal evidence of decreased awareness of symptoms has been reported in HD, few studies have investigated this area. Neuropsychological deficits seem to be particularly relevant among patients with early HD onset.
Many motor and non-motor symptoms in HD have been attributed to subcortical dysfunction (e.g., striatum) and the connecting circuitry with the frontal lobes [84]. For example, executive dysfunction on cognitive tasks (i.e., set shifting, response inhibition) has been linked with the dorsolateral subcortical circuit and dorsolateral prefrontal cortex deficits [85].
On the other hand, neuroleptic sensitivity may also impact apathy, in particular increasing sedation and emotional blunting [86].

3.7. Disinhibition, Impulsivity, and Sexual Disorders

Fewer studies have examined disinhibition, which includes impulsivity, hyperactivity, emotional lability and “acting out”, in HD and they have not found this symptom to be particularly prominent in these patients [83]. Changes in sexuality have been well documented in HD. Disorders of sexual functioning, such as hypoactive sexual desire and inhibited orgasm have been reported in men, with rates of 63% and 56%, respectively [87]. In female patients, 75% had hypoactive sexual desire, and 42% had inhibited orgasm. Also, sexual aberrations, such as sexual assault, promiscuity, incest, indecent exposure, and voyeurism, have all been described in HD [64]. The etiology of these abnormalities may be related to specific psychiatric syndromes prevalent in HD, such as mania, to the underlying neurotransmitter deficits of HD, or to medication effects. There is some evidence that male HD patients with both inhibited orgasm and increased sexual interest are at higher risk of developing paraphilias [88].
Hypersexual behavior is more prevalent in men, ranging from 3.9%–30% vs. 2.1%–25% in women [72,87,88]. In a pioneer study, Dewhurst et al. [72] reported in their article some social consequences of these symptoms. In 30 out of 102 patients studied, the authors found abnormal sexual behaviors, with 18.6% showing hypersexuality. In another study, Bolt [88] found that only 20 (6%) out of 334 patients had increased libido or sexual deviation, and Oliver [89] also reported 6% of patients displaying similar behavior.
Craufurd et al. interviewed 134 patients attending an HD management clinic using the Problem Behaviors Assessment for HD (PBA-HD) [36]. Uninhibited sexual behavior was reported by 6% of the patients, while demanding or persistent sexual behavior was described in 5% (Table 9) [38,88].
Table 9. Sexual dysfunction in mutation carriers.

3.8. Pre-Symptomatic HD and Psychiatric Disorders

Previous findings have suggested, although inconclusively, that psychopathology as well as cognitive dysfunction may precede the onset of motor symptoms in many patients [90,91]. Now, with the availability of a genetic test, it is possible to identify individuals who have CAG trinucleotide repeat expansion in the pathological range but are not yet showing sufficient motor signs for the diagnosis of clinical disease (i.e., pre-symptomatic gene carriers/subjects). Thus, it is now possible to study the relationship between genetic data and individuals’ characteristics before disease onset. Indeed, several studies have found subtle motor, cognitive, psychiatric, and neuroimaging abnormalities in HD years before diagnosis [92].
Regarding depressive symptoms, data on pre-symptomatic patients are still controversial, with some studies reporting a greater prevalence of MDD and depressive symptoms in both symptomatic and pre-symptomatic mutation carriers than non-carriers, and others reporting no differences [1,93]. From the existing literature, it is unclear how early behavioral manifestations of frontal dysfunction occur in HD. Duff et al. [19], using a pre-HD cohort, have previously reported on subtly elevated psychiatric symptoms in individuals prior to diagnosis. Some of these symptoms may reflect frontal disturbances (e.g., obsessive-compulsiveness, interpersonal sensitivity, hostility) in pre-HD. The authors hypothesized that pre-HD, expansion-positive individuals would report higher levels of frontal behaviors compared to expansion-negative individuals. Not only are apathy, disinhibition, and executive dysfunction more prevalent in the gene-expanded group, they are also associated with other markers of disease progression in HD.

4. Conclusions

Psychiatric disturbances are a constituent core of HD; this is known by the disease’s first description. The pathways leading to psychopathology in HD are still not completely clear. Indeed, several findings suggest that both neuropathology and environmental stress contribute to the occurrence of neuropsychiatric phenomena [15]. One characteristic feature is continuous change in the clinical presentation of symptoms, complicating nosography and pharmacological treatment.
It is clear that not only depression and anxiety are typical symptoms of HD, but also a number of other psychological, behavioral, and cognitive symptoms that may deeply impair quality of life of patients and relatives. Diagnosing and acknowledging the presence of psychopathology in HD is of major importance and may help patients and their families cope better with the severe symptoms of this progressive disease. It is thus vital to confront these problems from the beginning of the disease journey. First of all, diagnosis communication should be the first step of a long trip in which patients and relatives must know what is going to happen and how to face it [17]. Communication support and psychological counseling should then be guided by the knowledge of the psychiatric course that the disease could take. At the same time, a good communication channel should always be open to patients, relatives, and the medical team in order to enable timely response to the rise of psychiatric or cognitive symptoms. Pharmacological treatment should be properly used in a timely fashion (e.g., avoiding Xenazine in patients with severe depression at high risk of suicidality and preferring anti-impulsive treatment) in order to prevent breakdown and potential social and familial consequences. In addition, drug interactions should be also monitored to prevent adverse or even paradoxical reactions. An adequate symptomatic treatment can improve the quality of life of HD patients and their caregivers [94].
The HD treatment (psychopharmacological and/or psychological support) is based at present on a difficult integration of the still scarce experimental evidence and experience gained in the field, integration that is left to the clinician (or the clinical team), with indisputable and urgent decision-loading. In an attempt to define a good clinical practice in the context of HD, some treatment algorithms have been developed whose initial assumption remains the need for tailored interventions, responding not only to the patient’s overall health condition (co-morbidity and contraindications to treatment) but also to the patient’s needs and preferences.

Acknowledgments

No funds were received for this study.

Author Contributions

A.B. and R.A.P. designed the study protocol and performed the first search and related analyses; C.P., E.C. and E.Z. supported the second phase of the analysis, reading the article and commenting them with other authors; A.C. and V.S. read all the selected articles in order to figure out the most relevant issues, also comparing the actual literature with the historical pictures of HD. C.L. considered psychological and neuropsychological aspects of articles:, R.A.P., A.B. and LC wrote the first draft of the article and edited following revisions. All authors read, discussed and accepted the final version.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Van Duijn, E.; Kingma, E.M.; Timman, R.; Zitman, F.G.; Tibben, A.; Roos, R.A.; van der Mast, R.C. Cross-sectional study on prevalences of psychiatric disorders in mutation carriers of Huntington’s disease compared with mutation-negative first-degree relatives. J. Clin. Psychiatry 2008, 69, 1804–1810. [Google Scholar] [CrossRef] [PubMed]
  2. MacDonald, M.E.; Ambrose, C.M.; Duyao, M.P.; Myers, R.H.; Lin, C.; Srinidhi, L.; Barnes, G.; Taylor, S.A.; James, M.; Groot, N.; et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell 1993, 72, 971–983. [Google Scholar] [CrossRef]
  3. Bruyn, G.W. Huntington’s chorea: Historical, clinical and laboratory synopsis. In Handbook of Clinical Neurology; Vinken, P.J., Bruyn, G.W., Eds.; Elsevier: Amsterdam, The Netherlands, 1968; Volume 6, pp. 298–378. [Google Scholar]
  4. Gusella, J.F.; Wexler, N.S.; Conneally, P.M.; Naylor, S.L.; Anderson, M.A.; Tanzi, R.E.; Watkins, P.C.; Ottina, K.; Wallace, M.R.; Sakaguchi, A.Y.; et al. A polymorphic DNA marker genetically linked to Huntington’s disease. Nature 1983, 306, 234–238. [Google Scholar] [CrossRef] [PubMed]
  5. Anderson, K.E. Huntington’s disease, and related disorders. Psychiatr. Clin. North Am. 2005, 28, 275–290. [Google Scholar] [CrossRef] [PubMed]
  6. Ross, C.A.; Tabrizi, S.J. Huntington’s disease: From molecular pathogenesis to clinical treatment. Lancet Neurol. 2011, 10, 83–98. [Google Scholar] [CrossRef]
  7. Bano, D.; Zanetti, F.; Mende, Y.; Nicotera, P. Neurodegenerative processes in Huntington’s disease. Cell Death Dis. 2011, 2, e228. [Google Scholar] [CrossRef] [PubMed]
  8. Frank, S. Treatment of Huntington’s disease. Neurotherapeutics 2014, 11, 153–160. [Google Scholar] [CrossRef] [PubMed]
  9. Wexler, N.S.; Collett, L.; Wexler, A.R.; Rawlins, M.D.; Tabrizi, S.J.; Douglas, I.; Smeeth, L.; Evans, S.J. Incidence of adult Huntington’s disease in the UK: A UK-based primary care study and a systematic review. BMJ Open 2016, 6, e009070. [Google Scholar] [CrossRef] [PubMed]
  10. Pringsheim, T.; Wiltshire, K.; Day, L.; Dykeman, J.; Steeves, T.; Jette, N. The incidence and prevalence of Huntington’s disease: A systematic review and meta-analysis. Mov. Disord. 2012, 27, 1083–1091. [Google Scholar] [CrossRef] [PubMed]
  11. Fisher, E.R.; Hayden, M.R. Multisource ascertainment of Huntington disease in Canada: Prevalence and population at risk. Mov. Disord. 2014, 29, 105–114. [Google Scholar] [CrossRef] [PubMed]
  12. Squitieri, F.; Griguoli, A.; Capelli, G.; Porcellini, A.; D’Alessio, B. Epidemiology of Huntington disease: First post-HTT gene analysis of prevalence in Italy. Clin. Genet. 2016, 89, 367–370. [Google Scholar] [CrossRef] [PubMed]
  13. Roos, R.A. Huntington’s disease: A clinical review. Orphanet J. Rare Dis. 2010, 5, 40. [Google Scholar] [CrossRef] [PubMed]
  14. Losekoot, M.; van Belze, M.J.; Seneca, S.; Bauer, P.; Stenhouse, S.A.; Barton, D.E. EMQN/CMGS best practice guidelines for the molecular genetic testing of Huntington disease. Eur. J. Hum. Genet. 2013, 21, 480–486. [Google Scholar] [CrossRef] [PubMed]
  15. van Duijn, E.; Kingma, E.M.; van der Mast, R.C. Psychopathology in verified Huntington’s disease gene carriers. J. Neuropsychiatry Clin. Neurosci. 2007, 19, 441–448. [Google Scholar] [CrossRef] [PubMed]
  16. Bates, G.P.; Harper, P.J.L. Huntington’s Disease; Oxford University Press: Oxford, UK, 2002. [Google Scholar]
  17. Hamilton, J.M.; Salmon, D.P.; Corey-Bloom, J.; Gamst, A.; Paulsen, J.S.; Jerkins, S.; Jacobson, M.W.; Peavy, G. Behavioural abnormalities contribute to functional decline in Huntington’s disease. J. Neurol. Neurosurg. Psychiatry 2003, 74, 120–122. [Google Scholar] [CrossRef] [PubMed]
  18. Wheelock, V.L.; Tempkin, T.; Marder, K.; Nance, M.; Myers, R.H.; Zhao, H.; Kayson, E.; Orme, C.; Shoulson, I.; Huntington Study Group. Predictors of nursing home placement in Huntington disease. Neurology 2003, 60, 998–1001. [Google Scholar] [CrossRef] [PubMed]
  19. Duff, K.; Paulsen, J.S.; Beglinger, L.J.; Nance, M.; Myers, R.H.; Kayson, E.; Orme, C.; Shoulson, I. Psychiatric symptoms in Huntington’s disease before diagnosis: The predict-HD study. Biol. Psychiatry 2007, 62, 1341–1346. [Google Scholar] [CrossRef] [PubMed]
  20. Cummings, J.L. Behavioral and psychiatric symptoms associated with Huntington’s disease. In Behavioral Neurology of Movement Disorders; Weiner, W.J., Lang, A.E., Eds.; Raven Press: New York, NY, USA, 1995; pp. 179–186. [Google Scholar]
  21. Watt, D.C.; Seller, A. A clinico-genetic study of psychiatric disorder in Huntington’s chorea. Psychol. Med. Monogr. Suppl. 1993, 23, 1–46. [Google Scholar] [CrossRef]
  22. Reedeker, W.; van der Mast, R.C.; Giltay, E.J.; Kooistra, T.A.; Roos, R.A.; van Duijn, E. Psychiatric disorders in Huntington’s disease: A 2-year follow-up study. Psychosomatics 2012, 53, 220–229. [Google Scholar] [CrossRef] [PubMed]
  23. Murgod, U.A.; Saleem, Q.; Anand, A.; Brahmachari, S.K.; Jain, S.; Muthane, U.B. A clinical study of patients with genetically confirmed Huntington’s disease from India. J. Neurol. Sci. 2001, 190, 73–78. [Google Scholar] [CrossRef]
  24. Paulsen, J.S.; Ready, R.E.; Hamilton, J.M.; Mega, M.S.; Cummings, J.L. Neuropsychiatric aspects of Huntington’s disease. J. Neurol. Neurosurg. Psychiatry 2001, 71, 310–314. [Google Scholar] [CrossRef] [PubMed]
  25. Leroi, I.; O’Hearn, E.; Marsh, L.; Lyketsos, C.G.; Rosenblatt, A.; Ross, C.A.; Brandt, J.; Margolis, R.L. Psychopathology in patients with degenerative cerebellar diseases: A comparison to Huntington’s disease. Am. J. Psychiatry 2002, 159, 1306–1314. [Google Scholar] [CrossRef] [PubMed]
  26. Dooneief, G.; Mirabello, E.; Bell, K.; Marder, K.; Stern, Y.; Mayeux, R. An estimate of the incidence of depression in idiopathic Parkinson’s disease. Arch. Neurol. 1992, 49, 305–307. [Google Scholar] [CrossRef] [PubMed]
  27. Kulkantrakorn, K.; Jirapramukpitak, T. A prospective study in one year cumulative incidence of depression after ischemic stroke and Parkinson’s disease: A preliminary study. J. Neurol. Sci. 2007, 263, 165–168. [Google Scholar] [CrossRef] [PubMed]
  28. Morris, M. Psychiatric aspects of Huntington’s disease. In Huntington’s Disease; Harper, P.S., Ed.; WB Saunders: London, UK, 1991; Volume 22, pp. 81–126. [Google Scholar]
  29. van Duijn, E.; Craufurd, D.; Hubers, A.A.; Giltay, E.J.; Bonelli, R.; Rickards, H.; Anderson, K.E.; van Walsem, M.R.; van der Mast, R.C.; Orth, M.; et al. Neuropsychiatric symptoms in a European Huntington’s disease cohort (REGISTRY). J. Neurol. Neurosurg. Psychiatry 2014, 85, 1411–1418. [Google Scholar] [CrossRef] [PubMed]
  30. Epping, E.A.; Mills, J.A.; Beglinger, L.J.; Fiedorowicz, J.G.; Craufurd, D.; Smith, M.M.; Groves, M.; Bijanki, K.R.; Downing, N.; Williams, J.K.; et al. Characterization of depression in prodromal Huntington disease in the neurobiological predictors of HD (PREDICT-HD) study. J. Psychiatr. Res. 2013, 47, 1423–1431. [Google Scholar] [CrossRef] [PubMed]
  31. Thompson, J.C.; Harris, J.; Sollom, A.C.; Stopford, C.L.; Howard, E.; Snowden, J.S.; Craufurd, D. Longitudinal evaluation of neuropsychiatric symptoms in Huntington’s disease. J. Neuropsychiatry Clin. Neurosci. 2012, 24, 53–60. [Google Scholar] [CrossRef] [PubMed]
  32. Wetzel, H.H.; Gehl, C.R.; Dellefave-Castillo, L.; Schiffman, J.F.; Shannon, K.M.; Paulsen, J.S. Suicidal ideation in Huntington disease: The role of comorbidity. Psychiatry Res. 2011, 188, 372–376. [Google Scholar] [CrossRef] [PubMed]
  33. Anderson, K.E.; Gehl, C.R.; Marder, K.S.; Beglinger, L.J.; Paulsen, J.S.; Huntington’s Study Group. Comorbidities of obsessive and compulsive symptoms in Huntington’s disease. J. Nerv. Ment. Dis. 2010, 198, 334–338. [Google Scholar] [CrossRef] [PubMed]
  34. Julien, C.L.; Thompson, J.C.; Wild, S.; Yardumian, P.; Snowden, J.S.; Turner, G.; Craufurd, D. Psychiatric disorders in preclinical Huntington’s disease. J. Neurol. Neurosurg. Psychiatry 2007, 78, 939–943. [Google Scholar] [CrossRef] [PubMed]
  35. Marshall, J.; White, K.; Weaver, M.S.; Flury Wetherill, L.; Hui, S.; Stout, J.C.; Johnson, S.A.; Beristain, X.; Gray, J.; Wojcieszek, J.; et al. Specific psychiatric manifestations among preclinical Huntington disease mutation carriers. Arch. Neurol. 2007, 64, 116–121. [Google Scholar] [CrossRef] [PubMed]
  36. Paulsen, J.S.; Nehl, C.; Hoth, K.F.; Kanz, J.E.; Benjamin, M.; Conybeare, R.; McDowell, B.; Turner, B. Depression and stages of Huntington’s disease. J. Neuropsychiatry Clin. Neurosci. 2005, 17, 496–502. [Google Scholar] [CrossRef] [PubMed]
  37. Kirkwood, S.C.; Su, J.L.; Conneally, P.M.; Foroud, T. Progression of symptoms in the early and middle stages of Huntington disease. Arch. Neurol. 2001, 58, 273–278. [Google Scholar] [CrossRef] [PubMed]
  38. Craufurd, D.; Thompson, J.C.; Snowden, J.S. Behavioral changes in Huntington disease. Neuropsychiatry Neuropsychol. Behav. Neurol. 2001, 14, 219–226. [Google Scholar] [PubMed]
  39. Kulisevsky, J.; Litvan, I.; Berthier, M.L.; Pascual-Sedano, B.; Paulsen, J.S.; Cummings, J.L. Neuropsychiatric assessment of gilles de la tourette patients: Comparative study with other hyperkinetic and hypokinetic movement disorders. Mov. Disord. 2001, 16, 1098–1104. [Google Scholar] [CrossRef] [PubMed]
  40. Pflanz, S.; Besson, J.A.O.; Ebmeier, K.P.; Simpson, S. The clinical manifestation of mental disorder in Huntington’s disease: A retrospective case record study of disease progression. Acta Psychiatr. Scand. 1991, 83, 53–60. [Google Scholar] [CrossRef] [PubMed]
  41. Slaughter, J.R.; Martens, M.P.; Slaughter, K.A. Depression and Huntington’s disease: Prevalence, clinical manifestations, aetiology, and treatment. CNS Spectr. 2001, 6, 306–326. [Google Scholar] [CrossRef] [PubMed]
  42. Peyser, C.E.; Folstein, S.E. Huntington’s disease as a model for mood disorders. Clues from neuropathology and neurochemistry. Mol. Chem. Neuropathol. 1990, 12, 99–119. [Google Scholar] [CrossRef] [PubMed]
  43. Vonsattel, J.P.; Meyers, R.H.; Stevens, T.J.; Ferrante, R.J.; Bird, E.D.; Richardson, E.P., Jr. Neuropathological classification of Huntington’s disease. J. Neuropathol. Exp. Neurol. 1985, 44, 559–577. [Google Scholar] [CrossRef] [PubMed]
  44. Alexander, G.E.; De Long, M.R.; Strick, P.L. Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Ann. Rev. Neurosci. 1986, 9, 357–381. [Google Scholar] [CrossRef] [PubMed]
  45. Cummings, J.L. Frontal-subcortical circuits and human behavior. Arch. Neurol. 1993, 50, 873–880. [Google Scholar] [CrossRef] [PubMed]
  46. Gamez, J.; Lorenzo-Bosquet, C.; Cuberas-Borrós, G.; Carmona, F.; Hernández-Vara, J.; Castilló, J.; Castell-Conesa, J. Does reduced [(123)I]-FP-CIT binding in Huntington’s disease suggest pre-synaptic dopaminergic involvement? Clin. Neurol. Neurosurg. 2010, 112, 870–875. [Google Scholar] [CrossRef] [PubMed]
  47. Gamez, J.; Lorenzo-Bosquet, C.; Cuberas-Borrós, G.; Carmona, F.; Badía, M.; Castilló, J.; Badía, M.; de Fabregues, O.; Hernández-Vara, J.; Castell-Conesa, J. Progressive Presynaptic Dopaminergic Deterioration in Huntington Disease: A [123I]-FP-CIT SPECT Two-Year Follow-Up Study. Clin. Nucl. Med. 2013, 39, e227–e228. [Google Scholar] [CrossRef] [PubMed]
  48. Folstein, S.E.; Franz, M.L.; Jensen, B.A.; Chase, G.A.; Folstein, M.F. Conduct disorder and affective disorder among the offspring of patients with Huntington’s disease. Psychol. Med. 1983, 13, 45–52. [Google Scholar] [CrossRef] [PubMed]
  49. Zappacosta, B.; Monza, D.; Meoni, C.; Austoni, L.; Soliveri, P.; Gellera, C.; Alberti, R.; Mantero, M.; Penati, G.; Caraceni, T.; et al. Psychiatric symptoms do not correlate with cognitive decline, motor symptoms, or CAG repeat length in Huntington’s disease. Arch. Neurol. 1996, 53, 493–497. [Google Scholar] [CrossRef] [PubMed]
  50. Smith, M.M.; Mills, J.A.; Epping, E.A.; Westervelt, H.J.; Paulsen, J.S. Depressive symptom severity is related to poorer cognitive performance in prodromal Huntington disease. Neuropsychology 2012, 26, 664–669. [Google Scholar] [CrossRef] [PubMed]
  51. Mendez, M.F. Huntington’s disease: Update and review of neuropsychiatric aspects. Int. J. Psychiatry Med. 1994, 24, 189–208. [Google Scholar] [CrossRef] [PubMed]
  52. Hubers, A.A.; van Duijn, E.; Roos, R.A.; Craufurd, D.; Rickards, H.; Bernhard Landwehrmeyer, G.; van der Mast, R.C.; Giltay, E.J.; REGISTRY investigators of the European Huntington’s Disease Network. Suicidal ideation in a European Huntington’s disease population. J. Affect. Disord. 2013, 151, 248–258. [Google Scholar] [CrossRef] [PubMed]
  53. Hubers, A.A.; Reedeker, N.; Giltay, E.J.; Roos, R.A.; van Duijn, E.; van der Mast, R.C. Suicidality in Huntington’s disease. J. Affect. Disord. 2012, 136, 550–557. [Google Scholar] [CrossRef] [PubMed]
  54. Fiedorowicz, J.G.; Mills, J.A.; Ruggle, A.; Langbehn, D.; Paulsen, J.S. A Suicidal behavior in prodromal Huntington disease. Neurodegener. Dis. 2011, 8, 483–490. [Google Scholar] [CrossRef] [PubMed]
  55. Paulsen, J.S.; Hoth, K.F.; Nehl, C.; Stierman, L. Critical periods of suicide risk in Huntington’s disease. Am. J. Psychiatry 2005, 162, 725–731. [Google Scholar] [CrossRef] [PubMed]
  56. Berrios, G.E.; Wagle, A.C.; Marková, I.S.; Wagle, S.A.; Rosser, A.; Hodges, J.R. Psychiatric symptoms in neurologically asymptomatic Huntington’s disease gene carriers: A comparison with gene negative at risk subjects. Acta Psychiatr. Scand. 2002, 105, 224–230. [Google Scholar] [CrossRef] [PubMed]
  57. Kim, S.H.; Manes, F.; Kosier, T.; Robinson, R.G. Irritability following traumatic brain injury. J. Nerv. Ment. Dis. 1999, 187, 327–335. [Google Scholar] [CrossRef]
  58. Demark, J.; Gemeinhardt, M. Anger and its management for survivors of acquired brain injury. Brain Inj. 2002, 16, 91–108. [Google Scholar] [CrossRef] [PubMed]
  59. Pugh, R. An association between hostility and poor adherence to treatment in patients suffering from depression. Br. J. Med. Psychol. 1983, 56, 205–208. [Google Scholar] [CrossRef] [PubMed]
  60. Horesh, N.; Rolnick, T.; Iancu Dannon, P.; Lepkifker, E.; Apter, A.; Kotler, M. Anger, impulsivity and suicide risk. Psychother. Psychosom. 1997, 66, 92–96. [Google Scholar] [CrossRef] [PubMed]
  61. Asnis, G.M.; Kaplan, M.L.; van Praag, H.M.; Sanderson, W.C. Homicidal behaviors among psychiatric outpatients. Hosp. Community Psychiatry 1994, 45, 127–132. [Google Scholar] [CrossRef] [PubMed]
  62. Snaith, R.P.; Taylo, C.M. Irritability: Definition, assessment and associated factors. Br. J. Psychiatry 1985, 147, 127–136. [Google Scholar] [CrossRef] [PubMed]
  63. Snaith, R.P.; Constantopoulos, A.A.; Jardine, M.Y.; McGuffin, P. Clinical Scale for the Self-Assessment of Irritability. Br. J. Psychiatry 1978, 132, 164–171. [Google Scholar] [CrossRef] [PubMed]
  64. Reedeker, N.; Bouwens, J.A.; Giltay, E.J.; Le Mair, S.E.; Roos, R.A.; van der Mast, R.C.; van Duijn, E. Irritability in Huntington’s disease. Psychiatry Res. 2012, 200, 813–818. [Google Scholar] [CrossRef] [PubMed]
  65. Orth, M.; Handley, O.J.; Schwenke, C.; Dunnett, S.B.; Craufurd, D.; Ho, A.K.; Wild, E.; Tabrizi, S.J.; Landwehrmeyer, G.B.; The investigators of the European Huntington’s Disease Network. Observing Huntington’s Disease: The European Huntington’s Disease Network’s REGISTRY. PLoS Curr. 2010. [Google Scholar] [CrossRef] [PubMed]
  66. Marder, K.; Zhao, H.; Myers, R.H.; Cudkowicz, M.; Kayson, E.; Kieburtz, K.; Orme, C.; Paulsen, J.; Penney, J.B., Jr.; Siemers, E.; et al. Rate of functional decline in Huntington’s disease. Neurology 2000, 54, 452–458. [Google Scholar] [CrossRef] [PubMed]
  67. Witjes-Ané, M.N.W.; Zwinderman, A.H.; Tibben, A.; van Ommen, G.J.; Roos, R.A. Behavioural complaints in participants who underwent predictive testing for Huntington’s disease. J. Med. Genet. 2002, 39, 857–862. [Google Scholar] [CrossRef] [PubMed]
  68. Salloway, S.; Cummings, J. Subcortical disease and neuropsychiatric illness. J. Neuropsychiatry Clin. Neurosci. 1994, 6, 93–99. [Google Scholar] [PubMed]
  69. Mega, M.S.; Cummings, J.L. Frontal-subcortical circuits and neuropsychiatric disorders. J. Neuropsychiatry Clin. Neurosci. 1994, 6, 358–370. [Google Scholar] [PubMed]
  70. Anderson, K.E.; Louis, E.D.; Stern, Y.; Marder, KS. Cognitive correlates of obsessive and compulsive symptoms in Huntington’s disease. Am. J. Psychiatry 2001, 158, 799–801. [Google Scholar] [CrossRef] [PubMed]
  71. De Marchi, N.; Morris, M.; Mennella, R.; La Pia, S.; Nestadt, G. Association of obsessive-compulsive disorder and pathological gambling with Huntington’s disease in an Italian pedigree: Possible association with Huntington’s disease mutation. Acta Psychiatr. Scand. 1998, 97, 62–65. [Google Scholar] [CrossRef] [PubMed]
  72. De Marchi, N.; Mennella, R. Huntington’s disease and its association with psychopathology. Harv. Rev. Psychiatry 2000, 7, 278–289. [Google Scholar] [CrossRef] [PubMed]
  73. Dewhurst, K.; Oliver, J.; Trick, K.L.; McKnight, A.L. Neuro-psychiatric aspects of Huntington’s disease. Confin. Neurol. 1969, 31, 258–268. [Google Scholar] [CrossRef] [PubMed]
  74. Joel, D. Open interconnected model of basal ganglia-thalamocortical circuitry and its relevance to the clinical syndrome of Huntington’s disease. Mov. Disord. 2001, 16, 407–423. [Google Scholar] [CrossRef] [PubMed]
  75. Laplane, D.; Levasseur, M.; Pillon, B.; Dubois, B.; Baulac, M.; Mazoyer, B.; Tran Dinh, S.; Sette, G.; Danze, F.; Baron, J.C. Obsessive-compulsive and other behavioural changes with bilateral basal ganglia lesions. A neuropsychological, magnetic resonance imaging and positron tomography study. Brain 1989, 112, 669–725. [Google Scholar] [CrossRef]
  76. Beglinger, L.J.; Langbehn, D.R.; Duff, K.; Stierman, L.; Black, D.W.; Nehl, C.; Anderson, K.; Penziner, E.; Paulsen, J.S. Probability of obsessive and compulsive symptoms in Huntington’s disease. Biol. Psychiatry 2007, 61, 415–418. [Google Scholar] [CrossRef] [PubMed]
  77. Grabski, B.; Siwek, M.; Dudek, D.; Jaeschke, R.; Banaszkiewicz, K. Schizophrenia like psychotic symptoms in a patient with confirmed Huntington’s disease: A case report. Psychiatr. Polska 2012, 46, 665–675. [Google Scholar]
  78. Chuo, Y.P.; Hou, P.H.; Chan, C.H.; Lin, C.C.; Liao, Y.C. Juvenile Huntington’s disease presenting as difficult to treat seizure and the first episode of psychosis. Gen. Hosp. Psychiatry 2012, 34, 436.e9–436.e11. [Google Scholar] [CrossRef] [PubMed]
  79. Marin, R.S. Apathy: A neuropsychiatric syndrome. J. Neuropsychiatry Clin. Neurosci. 1991, 3, 243–254. [Google Scholar] [PubMed]
  80. Van Reekum, R.; Stuss, D.T.; Ostrander, L. Apathy: Why care? J. Neuropsychiatry Clin. Neurosci. 2005, 17, 7–19. [Google Scholar] [CrossRef] [PubMed]
  81. Starkstein, S.E.; Leentjes, A.F. The nosological position of apathy in clinical practice. J. Neurol. Neurosurg. Psychiatry 2008, 79, 1088–1092. [Google Scholar] [CrossRef] [PubMed]
  82. Boyle, P.A.; Malloy, P.F.; Salloway, S.; Cahn-Weiner, D.A.; Cohen, R.; Cummings, J.L. Executive dysfunction and apathy predict functional impairment in Alzheimer disease. Am. J. Geriatr. Psychiatry 2003, 11, 214–221. [Google Scholar] [CrossRef] [PubMed]
  83. Bamford, K.A.; Caine, E.D.; Kido, D.K.; Cox, C.; Shoulson, I. A prospective evaluation of cognitive decline in early Huntington’s disease: Functional and radiographic correlates. Neurology 1995, 45, 1867–1873. [Google Scholar] [CrossRef] [PubMed]
  84. Aylward, E.H.; Sparks, B.F.; Field, K.M.; Yallapragada, V.; Shpritz, B.D.; Rosenblatt, A.; Brandt, J.; Gourley, L.M.; Liang, K.; Zhou, H.; et al. Onset and rate of striatal atrophy in preclinical Huntington disease. Neurology 2004, 63, 66–72. [Google Scholar] [CrossRef] [PubMed]
  85. Bonelli, R.M.; Cummings, J.L. Frontal-subcortical dementias. Neurologist 2008, 14, 100–107. [Google Scholar] [CrossRef] [PubMed]
  86. Rosas, H.D.; Salat, D.H.; Lee, S.Y.; Zaleta, A.K.; Pappu, V.; Fischl, B.; Greve, D.; Hevelone, N.; Hersch, S.M. Cerebral cortex and the clinical expression of Huntington’s disease: Complexity and heterogeneity. Brain 2008, 131, 1057–1068. [Google Scholar] [CrossRef] [PubMed]
  87. Yanofski, J. The dopamine dilemma: Using stimulants and antipsychotics concurrently. Psychiatry (Edgmont) 2010, 7, 18–23. [Google Scholar] [PubMed]
  88. Fedoroff, J.P.; Peyser, C.; Franz, M.L.; Folstein, S.E. Sexual disorders in Huntington’s disease. J. Neuropsychiatry Clin. Neurosci. 1994, 6, 147–153. [Google Scholar] [PubMed]
  89. Bolt, J.M. Huntington’s chorea in the west of Scotland. Br. J. Psychiatry 1970, 116, 259–270. [Google Scholar] [CrossRef] [PubMed]
  90. Oliver, J.E. Huntington’s chorea in Northamptonshire. Br. J. Psychiatry 1970, 116, 241–253. [Google Scholar] [CrossRef] [PubMed]
  91. Di Maio, L.; Squitieri, F.; Napolitano, G.; Campanella, G.; Trofatter, J.A.; Conneally, P.M. Onset symptoms in 510 patients with Huntington’s disease. J. Med. Genet. 1993, 30, 289–292. [Google Scholar] [CrossRef] [PubMed]
  92. Kirkwood, S.C.; Siemers, E.; Hodes, M.E.; Conneally, P.M.; Christian, J.C.; Foroud, T. Subtle changes among presymptomatic carriers of the Huntington’s disease gene. J. Neurol. Neurosurg. Psychiatry 2000, 69, 773–779. [Google Scholar] [CrossRef] [PubMed]
  93. Aylward, E.H.; Codori, A.M.; Barta, P.E.; Pearlson, G.D.; Harris, G.J.; Brandt, J. Basal ganglia volume and proximity to onset in presymptomatic Huntington disease. Arch. Neurol. 1996, 53, 1293–1296. [Google Scholar] [CrossRef] [PubMed]
  94. Jensen, P.; Sørensen, S.A.; Fenger, K.; Bolwig, T.G. A study of psychiatric morbidity in patients with Huntington’s disease, their relatives, and controls. Admissions to psychiatric hospitals in Denmark from 1969 to 1991. Br. J. Psychiatry 1993, 163, 790–797. [Google Scholar] [PubMed]

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Repetitive Behaviours and Restricted Interests in Individuals with Down Syndrome—One Way of Managing Their World?
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