Evidence map›Paper›PMID 25550818›Full record

ArticleInternational journal of clinical and experimental pathology2014

Evidence of the presence of amyloid substance in the blood of familial amyloidotic polyneuropathy patients with ATTR Val30Met mutation.

Jinping Liu, Jie Lan, Peng Zhao, Fang Zheng, Jingjing Song, Peilan Zhang, Xuguo Sun

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 100% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study.Genetics in medicine : official journal of the American College of Medical Genetics · 2022
    Article
  2. 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

7 authors at 2 institutions in 1 country.

Jinping LiuDepartment of Neurology, Tianjin Medical University General Hospital Tianjin 300203, China.
Jie LanSchool of Medical Laboratory, Tianjin Medical University, Tianjin Medical University General Hospital Tianjin 300203, China.
Peng ZhaoDepartment of Neurology, Tianjin Medical University General Hospital Tianjin 300203, China.
Fang ZhengSchool of Medical Laboratory, Tianjin Medical University, Tianjin Medical University General Hospital Tianjin 300203, China.
Jingjing SongSchool of Medical Laboratory, Tianjin Medical University, Tianjin Medical University General Hospital Tianjin 300203, China.
Peilan ZhangDepartment of Neurology, Tianjin Huanhu Hospital Tianjin, China.
Xuguo SunSchool of Medical Laboratory, Tianjin Medical University, Tianjin Medical University General Hospital Tianjin 300203, China.
Tianjin Medical University General Hospital · CNTianjin Huanhu Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transthyretin (TTR) is a major amyloid fibril protein found in patients with familial amyloidotic polynuropathy (FAP) and senile systemic amyloidosis (SSA). Mainly synthesized in the live, TTR is transferred in the form of tetramer bound with thyroxine, retinol-binding protein (RBP) and lipoprotein in the blood. The aim of this study was to demonstrate the presence of amyloid substances in the blood by investigated the hemocoelom amyloid in different tissue sections from autopsies such as brain, kidney, heart and aorta arch tissue. Congo red staining was employed following by application of polarized light examination, to verify the presence of amyloid deposition in the tissues. Immunohistochemical staining was then performed to identify the specific type of amyloid deposition. Matrix-assisted laser desorption-ionization/time of flight mass spectrometry (MALDI-TOF/MS) was also used to analyze TTR mutation in FAP patients. All subjects were FAP ATTR Val30Met patients. In FAP patients, TTR amyloid deposition was found mainly in the tunica intima of the aortic arch. Interestingly, amyloid substance was found in the blood of FAP patient. Our results suggest that amyloid substance was present in the blood of FAP ATTR Val30Met patients.

Indexed as

MutationAdultAmyloidAmyloid Neuropathies, FamilialFemaleHumansMaleMiddle AgedPrealbuminSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAmyloidPrealbuminAmyloidCongo red stainingfamilial amyloidtic polynuropathyimmunohistochemistrytransthyretin

Identifiers

PMID25550818
PMCPMC4270544
OpenAlexW28389422

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.