Evidence map›Paper›PMID 40240329›Full record

ArticleNPJ Parkinson's disease2025

Spatial variations and precise location of substantia nigra hyperechogenicity in Parkinson's disease using TCS-MR fusion imaging.

Chao Hou, Wei Zhang, Hong-Bing Li, Shuo Li, Fang Nie, Xue-Mei Wang, Wen He

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Chao Hou *Department of Ultrasound, the Affiliated Hospital, Southwest Medical University, No. 25 Taiping Street, Jiangyang District, Luzhou, 646000, Sichuan, China.ORCID http://orcid.org/0000-0003-1234-8744
Wei Zhang *Department of Ultrasound, Beijing Tiantan Hospital, Capital Medical University, No.119, South Forth Ring Road West, Fengtai District, 100070, Beijing, China.
Hong-Bing LiDepartment of Ultrasound, Beijing Tiantan Hospital, Capital Medical University, No.119, South Forth Ring Road West, Fengtai District, 100070, Beijing, China.
Shuo LiDepartment of Ultrasound, Beijing Tiantan Hospital, Capital Medical University, No.119, South Forth Ring Road West, Fengtai District, 100070, Beijing, China.
Fang NieDepartment of Ultrasound, Lanzhou University Second Hospital, No.82 Cuiyingmen, Chengguan District, Lanzhou, 730030, Gansu, China.
Xue-Mei WangDepartment of Dyskinesia, Beijing Tiantan Hospital, Capital Medical University, No.119, South Forth Ring Road West, Fengtai District, 100070, Beijing, China. minnie02@sina.com.
Wen HeDepartment of Ultrasound, Lanzhou University Second Hospital, No.82 Cuiyingmen, Chengguan District, Lanzhou, 730030, Gansu, China. ttyyus_hewen@163.com.ORCID http://orcid.org/0000-0002-8427-971X

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82271995
6 · The paper itself

Abstract

Substantia nigra hyperechogenicity (SNH) assessed by transcranial sonography (TCS) is a neuroimaging biomarker of Parkinson's disease (PD), but its actual location and spatial changes are poorly understood. We aimed to evaluate the location and spatial progression of SNH in PD utilizing TCS-MR fusion imaging. This prospective study enrolled eighty-four PD patients and sixty-two controls. The plane with the largest area of red nucleus, the plane with the largest area of SNH, and the plane where the red nucleus is just out of view were selected and segmented, respectively, and echogenicity indices were calculated. SNH could present in SN, dorsal band of SN, red nucleus, and ventral tegmental area, and had two orientations. In the left midbrain, the anterior-posterior orientation had longer disease duration, larger SNH area, and higher Hoehn-Yahr stage than medial-lateral orientation. The anterior-posterior orientation and accumulation in various nuclei of SNH may serve as promising neuroimaging markers for PD progression.

Identifiers

PMID40240329
PMCPMC12003750

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.