Volume 29, Issue 4 pp. 1232-1237
SHORT COMMUNICATION

Impact of HIV impact on outcomes of deep-brain stimulation of the subthalamic nucleus for Parkinson’s disease

Jeanne Garcia

Jeanne Garcia

Department of Neurology, Rothschild Foundation Hospital, Paris, France

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Cécile Hubsch

Cécile Hubsch

Department of Neurology, Rothschild Foundation Hospital, Paris, France

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Ana Marques

Ana Marques

Department of Neurology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France

Contribution: Data curation (equal), Formal analysis (equal), Supervision (equal), Writing - review & editing (equal)

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Jean-Marc Gurruchaga

Jean-Marc Gurruchaga

Department of Neurosurgery, Henri-Mondor Hospital, Créteil, France

Contribution: Data curation (equal), Validation (equal), Writing - review & editing (equal)

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Cédric Lamirel

Cédric Lamirel

Clinical Research Unit, Rothschild Foundation Hospital, Paris, France

Contribution: Data curation (equal), Formal analysis (equal), Methodology (lead), Writing - review & editing (equal)

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Emmanuel Roze

Emmanuel Roze

Department of Neurology, Pitié–Salpêtrière Hospital, APHP, Sorbonne University, Inserm U 1127, CNRS UMR 7225, and UMR S 1127, Paris Brain Institute, Paris, France

Contribution: Data curation (equal), Methodology (equal), Validation (equal)

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Antoine Moulignier

Corresponding Author

Antoine Moulignier

Department of Neurology, Rothschild Foundation Hospital, Paris, France

Correspondence

Antoine Moulignier, Department of Neurology, Rothschild Foundation Hospital, 29, rue Manin, 75019 Paris, France.

Email: [email protected]

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First published: 30 December 2021

Abstract

Background and purpose

Middle-aged persons living with HIV (PLHIV) have a heightened risk of more concomitant age-related comorbidities that are acknowledged as signs of poorer prognosis after deep-brain stimulation of the subthalamic nucleus (STN-DBS) at younger-than-expected ages. To assess the beneficial and adverse effects of STN-DBS in PLHIV with Parkinson's disease (PD).

Methods

We retrospectively included nine PLHIV with PD who had sustained virological control. Patients were followed up for 7 ± 4 years.

Results

Patients’ mean ages at PD onset and STN-DBS were 45 ± 15 and 53 ± 16 years, respectively. At STN-DBS, mean HIV infection and PD durations were 15 ± 12 and 8 ± 4 years, respectively. STN-DBS significantly improved 1-year Unified Parkinson's Disease Rating Scale (UPDRS)-III scores (71%), daily off-time (63%), motor fluctuations (75%) and daily levodopa-equivalent dose (68%); mean 5-year UPDRS-III score and motor fluctuation improvements remained ~45%. Impulse control disorders (affecting 6/9 patients) fully resolved after STN-DBS. Postoperative course was uneventful. No serious adverse events occurred during follow-up.

Conclusion

Our findings indicate that STN-DBS is a safe and effective treatment for PLHIV with PD.

CONFLICT OF INTEREST

None.

DATA AVAILABILITY STATEMENT

Anonymized data will be shared on request by any qualified investigator provided that data transfer is in agreement with EU legislation on general data-protection regulations.

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