Evidence map›Paper›PMID 42528948›Full record

ArticleFrontiers in aging neuroscience2026

Clinical heterogeneity of Pisa syndrome across Lewy body disorders: a multicenter comparison of Parkinson's disease and dementia with Lewy bodies.

Zhou Su, Mengran Liu, Jun Kuai, Xinran Bao, Xia Guo, Meimei Zuo, Hao Wu, Jinghuan Gan, Shuai Liu, Yong Ji

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Article in Frontiers in aging neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zhou Su *Department of Neurology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Mengran Liu *School of Education, University of Bristol, Bristol, United Kingdom.
Jun KuaiDepartment of Gastroenterology, The First Affiliated Hospital of Henan Medical University, Xinxiang, Henan, China.
Xinran BaoDepartment of Neurology, First Hospital of Qinhuangdao, Hebei, China.
Xia GuoDepartment of Neurology, The First Affiliated Hospital of Baotou Medical College, Baotou, China.
Meimei ZuoDepartment of Neurology, Cangzhou People's Hospital, Cangzhou, China.
Hao WuTianjin Key Laboratory of Cerebrovascular and of Neurodegenerative Diseases, Department of Neurology, Tianjin Huanhu Hospital, Tianjin Dementia Institute, Tianjin, China.
Jinghuan GanDepartment of Neurology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Shuai LiuTianjin Key Laboratory of Cerebrovascular and of Neurodegenerative Diseases, Department of Neurology, Tianjin Huanhu Hospital, Tianjin Dementia Institute, Tianjin, China.
Yong JiTianjin Key Laboratory of Cerebrovascular and of Neurodegenerative Diseases, Department of Neurology, Tianjin Huanhu Hospital, Tianjin Dementia Institute, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pisa syndrome (PS) is well recognized in Parkinson's disease (PD) but has been less studied in dementia with Lewy bodies (DLB), and direct comparisons are scarce. The aim of this study is to compare the clinical expression of PS across PD and DLB. Methods: In this multicenter cross-sectional study, patients were classified as PD without PS ( Results: In both disorders, PS was associated with longer disease duration, worse daily functioning, and more recurrent falls. Significant disease × PS interactions were observed across cognitive, neuropsychiatric, gait, and fall outcomes. DLB-PS carried the heaviest cognitive and neuropsychiatric burden, whereas PD-PS showed the greatest motor and gait impairment. In PD, PS was independently associated with disease duration, MDS-UPDRS-III score, gait symmetry, and stride length. In DLB, PS was independently associated with lower attention and visuospatial/executive scores, greater hallucination severity, and a higher CDR stage. Attention/visuospatial dysfunction partly mediated the association between PS and recurrent falls in DLB, whereas gait asymmetry/stride impairment partly mediated the same association in PD. Conclusion: PS is not a uniform phenotype across Lewy body disorders. Our findings suggest that it behaves relatively more like a cognition-neuropsychiatry-associated axial syndrome in DLB, whereas in PD, it shows stronger associations with motor and gait features. The effect sizes are modest, indicating that PS is a multifactorial clinical sign rather than a strong predictor of any single domain.

Indexed as

dementia with Lewy bodiesgaitneuropsychiatric symptomsParkinson’s diseasePisa syndrome

Identifiers

PMID42528948
PMCPMC13416345

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