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Growth differentiation factor-15 as a negative predictor for microvascular obstruction in ST-segment elevation myocardial infarction after primary percutaneous coronary intervention
被引:1
|作者:
Wu, Xiang
[1
]
Bai, Jian
[1
]
Tan, Ying
[1
]
Wei, Zhonghai
[1
]
Dai, Qing
[1
]
Kang, Lina
[1
]
Wang, Lian
[1
]
Chen, Jianzhou
[1
]
Yang, Yining
[2
]
Wang, Kun
[1
]
Wu, Han
[1
]
机构:
[1] Nanjing Univ, Med Sch, Affiliated Hosp, Dept Cardiol,Nanjing Drum Tower Hosp, 321 Zhongshan Rd, Nanjing 210008, Peoples R China
[2] Nanjing Univ, Nanjing Drum Tower Hosp, Dept Echocardiog, Affiliated Hosp,Med Sch, Nanjing, Peoples R China
来源:
关键词:
Growth differentiation factor-15;
Microvascular obstruction;
ST-segment elevation myocardial infarction;
Predictor;
INTEGRIN ACTIVATION;
REPERFUSION INJURY;
GDF-15;
HEART;
D O I:
10.1007/s10554-024-03055-5
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Growth differentiation factor-15 (GDF-15) is an anti-inflammatory cytokine with cardioprotective effects, but circulating GDF-15 concentration predicts adverse cardiovascular outcomes in clinical settings. Microvascular obstruction (MVO) formation contributed to poor prognosis in patients with ST-segment elevation myocardial infarction (STEMI) after primary percutaneous coronary intervention (pPCI). We aimed to investigate GDF-15 concentration in relation to cardiac magnetic resonance (CMR)-derived MVO in STEMI patients after pPCI, which might help better understand the role of GDF-15 in STEMI. GDF-15 levels at 6 h after pPCI and MVO extent at day 5 +/- 2 after pPCI were measured in 74 STEMI patients (mean age 60.3 +/- 12.8 years, 86.5% men). The adjusted association of GDF-15 with MVO was analyzed with MVO treated as a categorized variable (extensive MVO, defined as MVO extent >= 2.6% of left ventricular (LV)) and a continuous variable (MVO mass, % of LV), respectively, in multivariate logistic and linear regression models. 41.9% of the patients developed extensive MVO after pPCI. In multivariate analysis, the odds ratio (95% confidential interval (CI)) of each standard deviation (SD) increase in GDF-15 for developing extensive MVO was 0.46 (0.21, 0.82), p = 0.02). Consistently, when MVO was used a continuous variable, each SD increase in GDF-15 was associated with a substantially lower MVO mass (beta - 0.42, standard error 0.19, p = 0.03). GDF-15 was a negative predictor for MVO in STEMI patients after pPCI. The observation was consistent with results from experiment studies, suggesting a potential protective effect of GDF-15 against cardiac injury.
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页码:863 / 871
页数:9
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