Evidence map›Paper›PMID 38886675›Full record

Observational studyBMC cardiovascular disorders2024

Combined effect of inflammation and malnutrition for long-term prognosis in patients with acute coronary syndrome undergoing percutaneous coronary intervention: a cohort study.

Yang Yuxiu, Xiaoteng Ma, Fei Gao, Tao Liu, Jianping Deng, Zhijian Wang

Abstract readObservational Study
In one paragraph

Observational study in BMC cardiovascular disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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

  1. Pooled it
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Article
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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

6 authors.

Yang Yuxiu *Department of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, 2 Anzhen Road, Chaoyang District, Beijing, 100037, China.
Xiaoteng Ma *Department of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, 2 Anzhen Road, Chaoyang District, Beijing, 100037, China.
Fei GaoDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, 2 Anzhen Road, Chaoyang District, Beijing, 100037, China.
Tao LiuDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, Nanchong, Sichuan, 637000, China.
Jianping DengDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, Nanchong, Sichuan, 637000, China. Djpdby@163.com.
Zhijian WangDepartment of Cardiology, Center for Coronary Artery Disease, Beijing Anzhen Nanchong Hospital, Capital Medical University, 2 Anzhen Road, Chaoyang District, Beijing, 100037, China. zjwang1975@hotmail.com.

Funding

Beijing Municipal Natural Science Foundation, the General Program 7232039Capital Health Research and Development of Special 2022-2-1052
6 · The paper itself

Abstract

backgroundInflammation is a key driver of atherosclerotic diseases and is often accompanied by disease-related malnutrition. However, the long-term burden of dysregulated inflammation with superimposed undernutrition in patients with acute coronary syndrome (ACS) remains unclear. This study sought to investigate the double burden and interplay of inflammation and malnutrition in patients with ACS undergoing percutaneous Coronary Intervention (PCI).

methodsWe retrospectively included 1,743 ACS patients undergoing PCI from June 2016 through November 2017 and grouped them according to their baseline nutritional and inflammatory status. Malnutrition was determined using the nutritional risk index (NRI) with a score lower than 100 and a high-inflamed condition defined as hs-CRP over 2 mg/L. The primary outcome was major adverse cardiovascular events (MACEs), compositing of cardiac mortality, non-fatal myocardial infarction, non-fatal stroke, and unplanned revascularization. Long-term outcomes were examined using the Kaplan-Meier method and compared with the log-rank test. Multivariable Cox proportional hazards regression analysis was applied to adjust for confounding. The reclassification index (NRI)/integrated discrimination index (IDI) statistics estimated the incremental prognostic impact of NRI and hs-CRP in addition to the Global Registry of Acute Coronary Events (GRACE) risk score.

resultsDuring a median follow-up of 30 months (ranges 30-36 months), 351 (20.1%) MACEs occurred. Compared with the nourished and uninflamed group, the malnourished and high-inflamed group displayed a significantly increased risk of MACEs with an adjusted hazard ratio of 2.446 (95% CI: 1.464-4.089; P < 0.001). The prognostic implications of NRI were influenced by patients' baseline inflammatory status, as it was only associated with MACEs among those high-inflamed (P for interaction = 0.005). Incorporating NRI and hs-CRP into the GRACE risk score significantly improved its predictive ability for MACEs (NRI: 0.210, P < 0.001; integrated discrimination index; IDI: 0.010, P < 0.001) and cardiac death (NRI: 0.666, P < 0.001; IDI: 0.023, P = 0.002).

conclusionsAmong patients with ACS undergoing PCI, the double burden of inflammation and malnutrition signifies poorer outcomes. Their prognostic implications may be amplified by each other and jointly improve the GRACE risk score's risk prediction performance.

Indexed as

Acute Coronary SyndromeInflammationMalnutritionNutritional StatusPercutaneous Coronary InterventionAgedBiomarkersFemaleHumansInflammation MediatorsMaleMiddle AgedNutrition AssessmentRetrospective StudiesRisk AssessmentRisk FactorsBiomarkersInflammation MediatorsAcute coronary syndromeInflammationMalnutritionNutritional risk index

Identifiers

PMID38886675
PMCPMC11181542

What OpenQuestion holds

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LicenceCC BY
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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.