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1.
Ned Tijdschr Geneeskd ; 160: A9359, 2016.
Article in Dutch | MEDLINE | ID: mdl-26732226

ABSTRACT

Impulse control disorders (ICD) in Parkinson's disease (PD) pose a therapeutic challenge. This article provides a description of the symptoms and management strategies of ICD in PD. We present two men aged 52 and 69 with ICD, especially hypersexuality, in response to dopaminergic medication. In the first case the symptoms of hypersexuality and gambling decreased after reducing the dose of the dopamine-agonist. In the second case the hypersexuality symptoms decreased after addition of naltrexon. It is important to recognize the symptoms of ICD in PD because of the large impact on social and relational functioning. It is of great importance to repeatedly ask the patient and their partner about these symptoms, since feelings of shame and guild hamper spontaneous report. The first step of treatment consists of reducing the dose of dopaminergic medication and/or to switch from dopamine-agonist to levodopa. Although the research on effective treatment options has been limited so far, treatment alternatives from the addiction field seem promising.


Subject(s)
Antiparkinson Agents/adverse effects , Disruptive, Impulse Control, and Conduct Disorders/chemically induced , Dopamine Agonists/adverse effects , Naltrexone/adverse effects , Parkinson Disease/complications , Sexual Dysfunction, Physiological/chemically induced , Aged , Antiparkinson Agents/therapeutic use , Disruptive, Impulse Control, and Conduct Disorders/prevention & control , Dopamine Agonists/therapeutic use , Humans , Male , Middle Aged , Naltrexone/therapeutic use , Narcotic Antagonists/adverse effects , Narcotic Antagonists/therapeutic use , Parkinson Disease/drug therapy , Sexual Dysfunction, Physiological/prevention & control , Treatment Outcome
2.
BMC Psychiatry ; 13: 277, 2013 Oct 31.
Article in English | MEDLINE | ID: mdl-24175936

ABSTRACT

Anorexia nervosa (AN) is a severe psychiatric disorder with high rates of morbidity, comorbidity and mortality, which in a subset of patients (21%) takes on a chronic course. Since an evidence based treatment for AN is scarce, it is crucial to investigate new treatment options, preferably focused on influencing the underlying neurobiological mechanisms of AN. The objective of the present paper was to review the evidence for possible neurobiological correlates of AN, and to hypothesize about potential targets for Deep brain stimulation (DBS) as a treatment for chronic, therapy-refractory AN. One avenue for exploring new treatment options based on the neurobiological correlates of AN, is the search for symptomatologic and neurobiologic parallels between AN and other compulsivity- or reward-related disorders. As in other compulsive disorders, the fronto-striatal circuitry, in particular the insula, the ventral striatum (VS) and the prefrontal, orbitofrontal, temporal, parietal and anterior cingulate cortices, are likely to be implicated in the neuropathogenesis of AN. In this paper we will review the few available cases in which DBS has been performed in patients with AN (either as primary diagnosis or as comorbid condition). Given the overlap in symptomatology and neurocircuitry between reward-related disorders such as obsessive compulsive disorder (OCD) and AN, and the established efficacy of accumbal DBS in OCD, we hypothesize that DBS of the nucleus accumbens (NAc) and other areas associated with reward, e.g. the anterior cingulated cortex (ACC), might be an effective treatment for patients with chronic, treatment refractory AN, providing not only weight restoration, but also significant and sustained improvement in AN core symptoms and associated comorbidities and complications. Possible targets for DBS in AN are the ACC, the ventral anterior limb of the capsula interna (vALIC) and the VS. We suggest conducting larger efficacy studies that also explore the functional effects of DBS in AN.


Subject(s)
Anorexia Nervosa/therapy , Deep Brain Stimulation , Anorexia Nervosa/physiopathology , Cerebral Cortex/physiopathology , Humans , Internal Capsule/physiopathology , Treatment Outcome , Ventral Striatum/physiopathology
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