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Antibody-mediated encephalitis: a treatable cause of schizophrenia

Published online by Cambridge University Press:  02 January 2018

Belinda R. Lennox*
Affiliation:
Cambridgeshire and Peterborough NHS Foundation Trust, and Department of Psychiatry, University of Cambridge, Addenbrooke's Hospital, Cambridge
Alasdair J. Coles
Affiliation:
Neurology Unit, Addenbrooke's Hospital, Cambridge
Angela Vincent
Affiliation:
Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK
*
Belinda R. Lennox, DM, MRCPsych, Department of Psychiatry, University of Cambridge, Herchel Smith Building, Cambridge Biomedical Campus, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK. Email: [email protected]
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Summary

Psychiatrists need to be vigilant for the newly recognised and treatable disorder of antibody-mediated encephalitis. Psychiatric symptoms are common, and individuals with the disorder often present initially to psychiatric services. We describe the clinical features of the disorder and make recommendations for further investigations.

Type
Editorials
Copyright
Copyright © 2012 The Royal College of Psychiatrists 

Psychiatry has been progressively demedicalised in the UK. The speciality has separated from the rest of medicine and there has been discussion about the relevance of biological models of psychiatric illness among some psychiatrists. Reference Bullmore, Fletcher and Jones1 This dangerous position is now exposed as new brain disorders have been described that are affecting patients currently under our management, which require medical investigation and management.

N-methyl-d-aspartate receptor antibody enchephalopathy

The most relevant disease is that associated with antibodies to the N-methyl-d-aspartate (NMDA) receptor. This was first described in young women who presented with a rapidly progressive neurological illness characterised by prolonged psychosis or disturbed behaviour, followed by a life-threatening state of autonomic instability, coma and dystonic movement disorder and with an underlying ovarian teratoma. Reference Dalmau, Tüzün, Wu, Masjuan, Rossi and Voloschin2 The antibodies are highly specific, demonstrably absent in large numbers of healthy and disease controls, Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3,Reference Dalmau, Lancaster, Martinez-Hernandez, Rosenfeld and Balice-Gordon4 and there is in vitro and in vivo evidence for their pathogenicity. Reference Dalmau, Lancaster, Martinez-Hernandez, Rosenfeld and Balice-Gordon4 Since 2007 there has been a large case series from a tertiary neurooncology centre in the USA Reference Dalmau, Gleichman, Hughes, Rossi, Peng and Lai5 and the first 44 cases from a neuroimmunology service in the UK, Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3 as well as many individual case reports. Reference Vincent, Bien, Irani and Waters6 These studies have broadened the clinical picture to include a wider age (5–80) and gender distribution (66–80% female) of patients, and showed that only a percentage (20–50%) of individuals had a detectable underlying paraneoplastic cause (usually an ovarian teratoma). The disorder has caused a high level of interest because of the severity of the clinical picture at nadir and the encouraging response to treatments if offered early in the course of the illness. In those with teratomas the removal of the tumour is essential, and even in the absence of tumour the disorder is usually substantially improved with immunotherapy. In both cases treatment is time critical – the sooner treatment is started the better the prognosis; Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3 thus early diagnosis is the key.

Even in the first case series, seizures and cognitive dysfunction were usually present but were dominated by the psychiatric features. The most common initial presentation (68–80%) was with symptoms of psychosis, with hallucinations, delusions, social withdrawal and thought disorder. Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3,Reference Dalmau, Gleichman, Hughes, Rossi, Peng and Lai5 There was then an inevitable progression, usually within a month, onto the second stage of more overt neurological features with movement disorder, characteristically of orofacial and choreoathetoid dyskinesias, epilepsy, autonomic disturbance and impaired consciousness often requiring admission to intensive care.

Subsequently, individuals with less severe progression have been identified and the clinical phenotype associated with these antibodies has expanded further. Individuals who were initially diagnosed as having encephalitis lethargic, neuroleptic malignant syndrome, catatonia or Hashimoto encephalopathy have had NMDA receptor antibodies. Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3

Voltage-gated potassium channel antibody enchephalopathy

The other condition that is of relevance is associated with antibodies against components of the voltage-gated potassium channel complex. These individuals usually present with amnesia and seizures, but they may also first present to psychiatric services with symptoms of agitation, hallucinations or behaviour change. Reference Vincent, Buckley, Schott, Baker, Dewar and Detert7 In a few cases, these individuals have been diagnosed initially as having a primary psychotic illness with the voltage-gated potassium channel complex antibodies only discovered following the development of hyponatraemia or seizures. Reference Parthasarathi, Harrower, Tempest, Hodges, Walsh and McKenna8 An increasing number of patients with these antibodies also have brief, dystonic faciobrachial dystonic seizures that can be misinterpreted as myclonic jerks. Reference Vincent, Bien, Irani and Waters6

Antibodies in cases of schizophrenia

In addition, we have described four cases of individuals with a DSM-IV diagnosis of schizophrenia with serum NMDA receptor or voltage-gated potassium channel complex antibodies, without a history of seizures, movement disorder or dysautonomia, even over 2 years of follow up. Reference Zandi, Irani, Lang, Waters, Jones and McKenna9 On this basis 6.5% (1.9–18.9% with 95% confidence intervals) of those with first-episode psychosis may have a psychiatric disorder associated with specific antibodies that are amenable to immunotherapy. In a review of all requests for NMDA receptor and voltage-gated potassium channel complex antibodies over the last 12 months through one tertiary neurological centre (Addenbrookes Hospital Cambridge, UK), the strongest predictor of a positive test result was a history of psychosis. Furthermore, 8 of the 16 individuals who were detected to be antibody-positive over this time have been under the management of psychiatric services. They had received diagnoses of schizophrenia (n = 6) and first-episode psychosis (n = 2). In addition, a novel but less common antibody directed against α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptors has been associated with atypical forms of psychosis and, in some cases, an underlying tumour. Reference Vincent, Bien, Irani and Waters6 The individuals with neurological conditions described in the literature to date could therefore represent the tip of the iceberg, although further work is needed to replicate findings and the clinical relevance of their cases.

Mechanisms of action

The mechanisms by which these antibodies produce a psychiatric phenotype is not clear but NMDA receptor dysfunction, in particular, has been a plausible explanation as the underlying mechanism for schizophrenia over the last 20 years. Kraepelin in his seminal classification of psychotic illnesses described a fluctuating confusional state and catatonic movement disorder alongside the psychotic symptoms and rapid cognitive deterioration in the disorder that he characterised as the catatonic form of dementia praecox, Reference Kraepelin and Robertson10 mirroring many of the symptoms seen in NMDA receptor antibody encephalitis. Indeed, NMDA-receptor blockade in vivo produces a range of schizophrenia-like symptoms in healthy individuals. Reference Pomarol-Clotet, Honey, Murray, Corlett, Absalom and Lee11 Ion channel disturbance and hyponatraemia have also been described as features of schizophrenia, previously attributed to medication-induced or psychogenic polydipsia.

Implications for clinical practice

There is, therefore, growing evidence that a proportion of schizophrenia may be antibody mediated and psychiatrists need to start to consider this aetiology in each presentation of first-episode psychosis. If positive, these patients should be considered for treatment with immunotherapy and have an underlying tumour excluded. This should be done, initially at least, in a centre that has experience in managing individuals with antibody-mediated disorders. Current recommendations, if paraneoplastic causes are excluded, are that individuals are aggressively treated with intravenous methylprednisolone and early reduction in the antibodies with plasma exchange, intravenous immunoglobulin or both, and combined with longer-term high-dose steroids or another immunosuppressive drug. Reference Dalmau, Tüzün, Wu, Masjuan, Rossi and Voloschin2,Reference Irani, Bera, Waters, Zuliani, Maxwell and Zandi3

Neurologists have already embraced and adopted this new clinical practice. Antibody screening in young people presenting with psychosis, seizures and cognitive disturbance is now part of routine clinical practice in neurological and intensive care settings. In the USA and the UK, antibody-associated encephalitis is now recognised to account for a significant minority of all cases of encephalitis and intensive care admissions. Reference Dalmau, Tüzün, Wu, Masjuan, Rossi and Voloschin2 The recognition of this cause of psychiatric presentations has required a shift in behaviour, with new collaborations with plasma exchange facilities, gynaecologists for ovarian teratoma removal and a challenge to nursing skills to manage the change in profile of patients on neurology wards. These changes have been managed because of the recognition of the treatment responsiveness of the condition, and facilitated by the co-location of these specialties. Psychiatry in contrast has been slow to respond, with current clinical practice being a long way removed from that of neurologists. Individuals with acute psychosis do not always see a psychiatrist for assessment in the UK, let alone have access to investigation. This is an untenable position, when there is the potential for detecting such a treatable disorder in a percentage of our patients. The physical and cultural separation of psychiatry from the rest of medicine makes it difficult for us now to adequately investigate and manage our patients.

Recommendations

We therefore recommend that all individuals with a first presentation of psychosis, or people with psychosis and features of autonomic disturbance, movement disorder, disorientation, seizures, hyponatraemia or rapid deterioration should be assessed with the possibility of antibody-mediated encephalitis in mind. This assessment should include, as a minimum, a neurological and cognitive examination and early serum testing for antibodies against the NMDA receptor and voltage-gated potassium channel. All patients testing positive for these serum antibodies should be referred to neurological centres with expertise in managing these cases. Cerebrospinal fluid is not usually required but the local immunology service should be consulted for advice. While awaiting antibody results, an electroencephalogram can be useful: encephalopathic features should prompt early referral. Magnetic resonance imaging of the brain may well be normal (although the finding of temporal lobe signal change on imaging is very suggestive of an antibody-mediated encephalopathy). The aim of these recommendations is the early identification and improved treatment for patients with this disorder and to bring medical investigation and management back to psychiatric practice.

Acknowledgements

We wish to thank Julia Deakin, Michael Zandi and Sarosh Irani for helpful comments in preparing this manuscript.

Footnotes

Declaration of interest

A.J.C. reports receiving consulting fees, lecture fees and grant support from Genzyme. A.V. and the Nuffield Department of Clinical Neuroscicences/University of Oxford, hold patents, receive royalties from Athena Diagnostics and receive payments for antibody assays.

Belinda R. Lennox (pictured) is HEFCE clinical senior lecturer and honorary consultant psychiatrist. Her research is on the biological basis of psychosis. Alasdair J. Coles is senior lecturer and honorary consultant neurologist. His research is on the immunological basis of brain disorders. Angela Vincent is a professor of neuroimmunology, leading research on autoimmunity in neurological disorders and heading the international referral centre for the diagnosis of immune-mediated neurological diseases.

References

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