Groaning in Progressive Supranuclear Palsy: Insights From a Large Asian Cohort
BACKGROUND: Although regularly encountered, the groaning phenomenon in progressive supranuclear palsy (PSP) currently lacks systematic investigation. OBJECTIVES: We investigated the frequency and clinical phenomenology of groaning in PSP. METHODS: We assessed 180 patients with PSP, identifying groaning through examination and history. A specially designed questionnaire captured groaning characteristics (intensity, frequency, and triggers). Scores for the PSP Clinical Deficits Scale (PSP-CDS), Barthel Index (BI), Short Cognitive and Neuropsychiatric Assessment (ShoCo) Scale, and modified Zarit Burden Interview (ZBI), and whole exome sequencing (WES) data, were extracted from our research database. RESULTS: Thirty-six (20.0%) patients exhibited groaning, most of whom (77.8%) had Richardson's syndrome (PSP-RS), which predicted groaning with an odds ratio (OR) of 4.1 (95% CI = 1.7-10.3, P = 0.002). Worse disease severity (PSP-CDS) was also a predictive factor (OR = 1.2, 95% CI = 1.1-1.3, P = 0.002). Additionally, patients with groaning demonstrated worse longitudinal disease trajectory, alongside significantly greater functional disability (BI), cognitive-behavioral impairment (ShoCo), and caregiver burden (ZBI). Groaning was typically moderate in intensity or loud, considered troublesome by caregivers and/or patients, and triggers or reasons were commonly identified (in 76.0%). WES showed several patients carrying pathogenic/likely pathogenic variants in genes potentially relevant to PSP (MAPT, GBA1, and SMPD1), but none carried the rare NEFH variant previously linked to familial moaning (p.Ile245Met). CONCLUSIONS: Our study provides insights into a poorly understood feature of PSP and highlights a troublesome symptom that is associated with substantial patient and caregiver burden. Further work is needed to investigate the pathophysiological basis of groaning and to develop effective therapies for it.
Authors
- Yi Jayne Tan (ORCID: https://orcid.org/0000-0003-1486-4734)
- Chin‐Hsien Lin (ORCID: https://orcid.org/0000-0001-8566-7573)
- Tzi Shin Toh (ORCID: https://orcid.org/0000-0003-2434-2147)
- Adeline Su Lyn Ng (ORCID: https://orcid.org/0000-0001-8822-8496)
- Yuan Ye Beh (ORCID: https://orcid.org/0000-0002-7875-3163)
- Eng‐King Tan (ORCID: https://orcid.org/0000-0003-2977-9743)
- Shen‐Yang Lim (ORCID: https://orcid.org/0000-0002-6942-2522)
- Yi Wen Tay (ORCID: https://orcid.org/0000-0002-9319-0768)
- Ai Huey Tan (ORCID: https://orcid.org/0000-0002-2979-3839)
- Kah Hui Yap (ORCID: https://orcid.org/0000-0002-7877-2997)
- Azlina Ahmad‐Annuar (ORCID: https://orcid.org/0000-0001-6329-4366)
- Andrew Leslie Lee
- Kai Shi Lim
- Anis Nadhirah Khairul Anuar (ORCID: https://orcid.org/0000-0001-8077-4265)
- Yi Zhe Lim
- Jeremy Christopher Fernandiz
- Jeffrey Wei Yang Tee
- Emilie Sing Yee Wong
- Darren Wan Pin Lim
- Ting Qing Lim
- Yi Xuan Tee
- Kelly Kher Nie Chen
- Jun Ping Chua (ORCID: https://orcid.org/0009-0006-4799-6118)
- Pin‐Shiuan Chen (ORCID: https://orcid.org/0000-0003-3992-1942)
- Christos Ganos
- Lu Yian Tan (ORCID: https://orcid.org/0009-0009-6762-0064)
Institutions
- University of Nottingham (GB)
- National Taiwan University (TW)
- Toronto Western Hospital (CA)
- Nottingham General Hospital (GB)
- Nottingham City Hospital (GB)
- University of Malaya (MY)
- Duke-NUS Medical School (SG)
- National Neuroscience Institute (SG)
- National Taiwan University Hospital (TW)
- Ontario Brain Institute (CA)
- Krembil Brain Institute
Publication Details
- Journal
- Movement Disorders Clinical Practice
- Published
- 2026-09-06
- DOI
- https://doi.org/10.1002/mdc3.70785
- Primary Topic
- Parkinson's Disease Mechanisms and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00