Evidence map›Paper›PMID 36312019›Full record

ArticleFrontiers in neuroscience2022

Altered serum amyloid beta and cerebral perfusion and their associations with cognitive function in patients with subcortical ischemic vascular disease.

Wei Zhang, Mingxu Li, Xia Zhou, Chaojuan Huang, Ke Wan, Chenchen Li, Jiabin Yin, Wenming Zhao, Cun Zhang, Xiaoqun Zhu and 1 more

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Article
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

11 authors.

Wei ZhangDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Mingxu LiDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xia ZhouDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Chaojuan HuangDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Ke WanDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Chenchen LiDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Jiabin YinDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Wenming ZhaoDepartment of Radiology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Cun ZhangDepartment of Radiology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Xiaoqun ZhuDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.
Zhongwu SunDepartment of Neurology, First Affiliated Hospital of Anhui Medical University, Hefei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subcortical ischemic vascular disease (SIVD) is one of the important causes of cognitive dysfunction, altered amyloid-beta (Aβ) and cerebral perfusion may be involved in the pathophysiological mechanism of SIVD and are closely related to cognitive function. We aimed to investigate altered serum Aβ and cerebral perfusion in patients with SIVD and their correlation with cognitive function. Seventy-four healthy controls (HCs) and 74 SIVD patients, including 38 SIVD patients with no cognitive impairment (SIVD-NCI) and 36 SIVD patients with mild cognitive impairment (SIVD-MCI) underwent the measurement of serum Aβ40 and Aβ42 levels, pseudo-continuous arterial spin labeling MRI scanning, and cognitive evaluation. Compared to the healthy controls (HCs), the level of serum Aβ40 and Aβ40/42 ratio increased and Aβ42 decreased in SIVD patients. The serum Aβ40 level and Aβ40/42 ratio in patients with SIVD-MCI were significantly higher than those in the HCs and SIVD-NCI, and the level of Aβ42 in the SIVD-MCI was lower than the HCs. In addition, the serum Aβ40/42 ratio provided high diagnostic accuracy for SIVD and SIVD-MCI, it was further identified as an independent risk factor for cognitive impairment. Patients with SIVD-NCI and SIVD-MCI exhibited both increased and decreased cerebral blood flow (CBF) in regional. The Aβ40/42 ratio was associated with global CBF, while altered global and regional CBF was associated with cognitive deficits. In addition, white matter hyperintensities volume (WMHV) correlated with Aβ40/42 ratio, CBF, and cognition. The relationship between Aβ40/42 ratio and cognition was partially mediated by altered CBF. Based on these results, we conclude that the serum Aβ40/42 ratio may be a potential biomarker that can complement current methods for the prediction and diagnosis of cognitive impairment in SIVD patients. In addition, serum Aβ may play a role in cognitive function by regulating CBF, which provides new insights into the intervention, treatment, and prevention of cognitive impairment in SIVD.

Indexed as

arterial spin labelingbiomarkercognitive impairmentserum amyloid betasubcortical ischemic vascular disease

Identifiers

PMID36312019
PMCPMC9608371

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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.