Anna Punga
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Professor of clinical Neurophysiology
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About
Professor Anna Punga is a faculty member in the Department of Clinical Neurophysiology at Uppsala Universitet, Sweden. Her research focuses on myasthenia gravis, including blood biomarkers, treatment guidelines, and pregnancy outcomes for affected women. She has published several articles addressing autoimmune encephalitis, neuronal antibody testing, and innovative approaches to physical therapy for patients with myasthenia gravis.
Recent Grants
Grant: Close
Elucidation of miRNAs in model diseases of autoimmune etiology and neuromuscular transmission
Open Date: 2015-03-01
Close Date: 2018-02-01
Grant: Close
miRNA som nya potentiella biomarkörer hos patienter med den kroniska neuromuskulära sjukdomen myasthenia gravis (MG)
Open Date: 2014-05-01
Close Date: 2016-05-01
Grant: Close
miRNA som nya potentiella biomarkörer hos patienter med den kroniska neuromuskulära sjukdomen myasthenia gravis (MG).
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Articles (14)
Year:
2025
Background Generalized myasthenia gravis (MG) with antibodies against the acetylcholine receptor is a chronic disease causing muscle weakness. Access to novel treatments warrants authoritative treatment recommendations. The Nordic countries have similar, comprehensive health systems, mandatory health registers, and extensive MG research. Methods MG experts and patient representatives from the five Nordic countries formed a working group to prepare treatment guidance for MG based on a systematic literature search and consensus meetings. Results Pyridostigmine represents the first‐line symptomatic treatment, while ambenonium and beta adrenergic agonists are second‐line options. Early thymectomy should be undertaken if a thymoma, and in non‐thymoma patients up to the age of 50–65 years if not obtaining remission on symptomatic treatment. Most patients need immunosuppressive drug treatment. Combining corticosteroids at the lowest possible dose with azathioprine is recommended, rituximab being an alternative first‐line option. Mycophenolate, methotrexate, and tacrolimus represent second‐line immunosuppression. Plasma exchange and intravenous immunoglobulin are used for myasthenic crises and acute exacerbations. Novel complement inhibitors and FcRn blockers are effective and fast‐acting treatments with promising safety profiles. Their use depends on local availability, refunding policies, and cost–benefit analyses. Adapted physical training is recommended. Planning of pregnancies with optimal treatment, information, and awareness of neonatal MG is necessary. Social support and adaptation of work and daily life activities are recommended. Conclusions Successful treatment of MG rests on timely combination of different interventions. Due to spontaneous disease fluctuations, comorbidities, and changes in life conditions, regular long‐term specialized follow‐up is needed. Most patients do reasonably well but there is room for further improvement. Novel treatments are promising, though subject to restricted access due to costs.
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2024
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2024
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2024
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2023
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2023
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2023
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2023
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2023
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2022
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2022
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2021
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2020
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2020
Collaborators (10)
Joachim Burman
Uppsala University
Christoffer Ehrstedt
department of pediatrics king fahad hospital of university
Fredrik Piehl
Karolinska Institutet
Andreas Meisel
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Amol K. Bhandage
Researcher/Docent/Associate Professor
Uppsala University
Tanel Punga
Uppsala University
John Vissing
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David Beeson
University of Oxford
Jee Woong Lee
Seoul National University
Sidsel Madsen
Aarhus University
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