Prognostic Value of Plasma Immunoglobulin G N-Glycome Traits in Pulmonary Arterial Hypertension.

2024-09
Journal of the American College of Cardiology 84(12)
- Ze-Jian Zhang
- Chao Liu
- Jie-Ling Ma
- Jing-Si Ma
- Jia Wang
- Ruo-Nan Li
- Dan Lu
- Yu-Ping Zhou
- Tian-Yu Lian
- Si-Jin Zhang
- Jing-Hui Li
- Lan Wang
- Kai Sun
- Chun-Yan Cheng
- Wen-Hui Wu
- Xin Jiang
- Zhi-Cheng Jing

PubMed: 39260931
DOI: 10.1016/j.jacc.2024.05.077

Study Design

Type: Observational
Sample size: n = 349
Population: 622 PAH patients from 2 national centers (Beijing [discovery] cohort: n = 273; Shanghai [validation] cohort: n = 349)
Methods: Cohort study; plasma IgG N-glycomes profiled by robust mass spectrometry-based method; Cox regression and Kaplan-Meier survival analyses; Harrell C-indexes

Background

B-type natriuretic peptide or N-terminal pro-B-type natriuretic peptide is the only blood biomarker in established risk calculators for pulmonary arterial hypertension (PAH). Profiling systemic-originated plasma immunoglobulin G (IgG) N-glycans, which reflect different components of the pathophysiology of PAH including immune dysregulation and inflammation, may improve PAH risk assessment.

Objectives

This study sought to identify plasma IgG N-glycan biomarkers that predict survival in PAH to improve risk assessment.

Methods

This cohort study examined 622 PAH patients from 2 national centers (Beijing [discovery] cohort: n = 273; Shanghai [validation] cohort: n = 349). Plasma IgG N-glycomes were profiled by a robust mass spectrometry-based method. Prognostic IgG N-glycan traits were identified and validated in the 2 cohorts using Cox regression and Kaplan-Meier survival analyses. The added value of IgG N-glycan traits to previously established risk models was assessed using Harrell C-indexes and survival analysis.

Results

Plasma IgG fucosylation was found to predict survival independent of age and sex in the discovery cohort (HR: 0.377; 95% CI: 0.168-0.845; P = 0.018) with confirmation in the validation cohort (HR: 0.445; 95% CI: 0.264-0.751; P = 0.005). IgG fucosylation remained a robust predictor of mortality in combined cohorts after full adjustment and in subgroup analyses. Integrating IgG fucosylation into previously established risk models improved their predictive capacity, marked by an overall elevation in Harrell C-indexes. IgG fucosylation was useful in further stratifying the intermediate-risk patients classified by a previously established model.

Conclusions

Plasma IgG fucosylation informs PAH prognosis independent of established factors, offering additional value for predicting PAH outcomes.