Evidence map›Paper›PMID 38252229›Full record

ArticleAnnals of nuclear medicine2024

Performance of

Honghui Guo, Sha Wu, Xin Xiang, Shuai Wang, Zhihui Fang, Qianchun Ye, Yao Zou, Yunhua Wang, Daoquan Peng, Xiaowei Ma

Abstract read
PubMed Publisher
In one paragraph

Article in Annals of nuclear medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

10 authors at 2 institutions in 1 country.

Honghui GuoDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
Sha WuDepartment of Cardiovascular Medicine, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.
Xin XiangDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
Shuai WangDepartment of Cardiovascular Medicine, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China.
Zhihui FangDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
Qianchun YeDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
Yao ZouDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
Yunhua WangDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China. wangyunhua0801@csu.edu.cn.
Daoquan PengDepartment of Cardiovascular Medicine, The Second Xiangya Hospital of Central South University, Changsha, 410011, Hunan, China. pengdaoquan@csu.edu.cn.
Xiaowei MaDepartment of Nuclear Medicine, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China. maxiaowei@csu.edu.cn.
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

Natural Science Foundation of Hunan Province 2020JJ4801the Research and Development Program of Hunan Province of China 2019SK2252the Research and Development Program of Hunan Province of China 2022SK2035
6 · The paper itself

Abstract

objectiveMost reported research has primarily investigated wild-type transthyretin cardiac amyloidosis (ATTRwt-CA). However, the application of bone scintigraphy for hereditary transthyretin cardiac amyloidosis (ATTRv-CA) has not been systematically investigated. Therefore, in this study, we aimed to evaluate the diagnostic value of

methodsFifty-four patients were enrolled in a highly suspected cardiac amyloidosis cohort. Transthyretin (TTR) gene characteristics were summarized in the ATTRv-CA group. In

resultsTwenty-eight patients were diagnosed with ATTRv-CA with eight genotypes. The Ala97Ser genotype accounts for 46% (n = 13) with a mean age of disease onset, definite diagnosis, and interval of 61.6 ± 1.9, 66.5 ± 1.3, and 4.0 (3.0, 6.2) years, respectively. Their VGS is Grade 3, and their H/CL ratio is higher than that of the non-Ala97Ser group, but no statistical significance exists (mean H/CL: 1.95 ± 0.06 vs. 1.87 ± 0.02, p = 0.844). Additionally, ATTRv-CA patients showed VGS ≥ 2, and mean H/CL ratio of 2.09 ± 0.06. The sensitivity and specificity of VGS were 100% and 65%, respectively. And the interobserver consistency analysis of VGS showed the intraclass correlation coefficient is 0.522. The best cutoff value of H/CL ratio was 1.51 (AUC = 0.996), and the diagnostic consistency of H/CL (bias: 0.018) was high.

conclusionsAla97Ser is the most common genotype in ATTRv-CA in our cohort, with characteristics of later onset and rapid progression, but delayed diagnosis and extensive

Indexed as

Amyloid Neuropathies, FamilialCardiomyopathiesHeartHumansPrealbuminRadionuclide ImagingTechnetium Tc 99m PyrophosphatePrealbuminTechnetium Tc 99m Pyrophosphate99mTc-PYPAla97Ser gene mutationHereditary transthyretin cardiac amyloidosis (ATTRv-CA)Semiquantitative parameterSingle-photon emission computed tomography

Identifiers

PMID38252229
OpenAlexW4391109690

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.