This study aims to analyse hyperechoic substantia nigra (HSN) characteristics and the correlation of HSN with clinical features and blood biomarkers in patients with Parkinson's disease (PD). Transcranial sonography (TCS) evaluations of the substantia nigra (SN) were performed in 40 healthy controls and 71 patients with PD, including patients with SN hyperechogenicity (SN+) and those with normal SN echogenicity (SN-). Evaluation of motor and non-motor symptoms was assessed by a series of rating scales. The uricase method was used to determine serum uric acid (UA) levels, and enzyme-linked immunosorbent assay (ELISA) was used to measure plasma interleukin (IL)-1 beta levels. TCS showed 92.50% specificity and 61.97% sensitivity in differentiating PD patients from controls. The area of SN+ contralateral to the side of initial motor symptoms (SNcontra) was larger than that ipsilateral to the side of initial motor symptoms (SNipsi). The PDSN+ group had lower Argentine Hyposmia Rating Scale (AHRS) scores and UA levels than the PDSN- group. Binary logistic regression analysis revealed that AHRS scores and UA levels could be independent predictors for HSN. The larger SN echogenic area (SNL) sizes positively correlated with plasma IL-1 beta levels in PD patients with SN+. The present study provides further evidence of the potential of SN echogenicity as an imaging biomarker for PD diagnosis. PD patients with HSN have more severe non-motor symptoms of hyposmia. HSN in PD patients is related to the mechanism of abnormal iron metabolism and microglial activation. Transcranial sonography (TCS) has potential as a tool for Parkinson's disease (PD) diagnosis. Hyperechoic substantia nigra (HSN) is a stable marker during the course of PD and does not reflect disease progression. PD patients with HSN have severer non-motor symptoms of hyposmia. HSN in PD patients is related to the mechanism of abnormal iron metabolism and microglial activation. image
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil
Bar-Seng-Shu, Edson
Almeida, Kelson James
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil
Almeida, Kelson James
de Andrade, Daniel Ciampi
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil
de Andrade, Daniel Ciampi
Fonoff, Erich Talamoni
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil
Fonoff, Erich Talamoni
Teixeira, Manoel Jacobsen
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil
Teixeira, Manoel Jacobsen
Barbosa, Egberto Reis
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Univ Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, BrazilUniv Sao Paulo, Hosp Clin, Div Cirurgia Neurol, Sch Med FMUSP, BR-05403000 Sao Paulo, Brazil