Evidence map›Paper›PMID 24711674›Full record

ArticleDisease markers2014

Calcium channel autoantibodies predicted sudden cardiac death and all-cause mortality in patients with ischemic and nonischemic chronic heart failure.

Haiyun Yu, Juanhui Pei, Xiaoyan Liu, Jingzhou Chen, Xian Li, Yinhui Zhang, Ning Li, Zengwu Wang, Ping Zhang, Kejiang Cao and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Frontiers in cardiovascular medicine · 2021
    Article
  3. Review
  4. Review
  5. Review
  6. 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

11 authors at 3 institutions in 1 country.

Haiyun YuState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Juanhui PeiState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Xiaoyan LiuState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Jingzhou ChenState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Xian LiState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Yinhui ZhangState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Ning LiState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Zengwu WangState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.
Ping ZhangPeople's Hospital, Peking University, Beijing 100044, China.
Kejiang CaoFirst People's Hospital of Jiangsu Province, Nanjing 210029, China.
Jielin PuState Key Laboratory of Cardiovascular Disease, Physiology and Pathophysiology Laboratory, Fu wai Cardiovascular Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, No. 167 Bei-Li-Shi Road, Xi-Cheng District, Beijing 100037, China.ORCID 0000-0003-0746-955X
Chinese Academy of Medical Sciences & Peking Union Medical College · CNJiangsu Province Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to evaluate whether CC-AAbs levels could predict prognosis in CHF patients. A total of 2096 patients with CHF (841 DCM patients and 1255 ICM patients) and 834 control subjects were recruited. CC-AAbs were detected and the relationship between CC-AAbs and patient prognosis was analyzed. During a median follow-up time of 52 months, there were 578 deaths. Of these, sudden cardiac death (SCD) occurred in 102 cases of DCM and 121 cases of ICM. The presence of CC-AAbs in patients was significantly higher than that of controls (both P < 0.001). Multivariate analysis revealed that positive CC-AAbs could predict SCD (HR 3.191, 95% CI 1.598-6.369 for DCM; HR 2.805, 95% CI 1.488-5.288 for ICM) and all-cause mortality (HR 1.733, 95% CI 1.042-2.883 for DCM; HR 2.219, 95% CI 1.461-3.371 for ICM) in CHF patients. A significant association between CC-AAbs and non-SCD (NSCD) was found in ICM patients (HR = 1.887, 95% CI 1.081-3.293). Our results demonstrated that the presence of CC-AAbs was higher in CHF patients versus controls and corresponds to a higher incidence of all-cause death and SCD. Positive CC-AAbs may serve as an independent predictor for SCD and all-cause death in these patients.

Indexed as

Death, Sudden, CardiacAdultAgedAutoantibodiesBiomarkersCalcium Channels, L-TypeCase-Control StudiesChronic DiseaseFemaleHeart FailureHumansKaplan-Meier EstimateMaleMiddle AgedMyocardial IschemiaPrognosisAutoantibodiesBiomarkersCalcium Channels, L-Type

Identifiers

PMID24711674
PMCPMC3966345
OpenAlexW2008571699

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.