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Published on: February 26, 2013
Cardio-kidney-metabolic complexity in patients with atrial fibrillation: an analysis from the prospective GLORIA-AF
Giulio Francesco Romiti1,2, Davide Antonio Mei1,3, Bernadette Corica1,3
1Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart & Chest Hospital, Liverpool, UK.
Insights
Cardio-Kidney-Metabolic (CKM) syndrome domains are common in atrial fibrillation (AF) patients. Increased CKM domains correlate with lower oral anticoagulant use and higher risks of death and cardiovascular events.
Area of Science:
- Cardiology
- Nephrology
- Metabolic Disorders
Background:
- Cardio-Kidney-Metabolic (CKM) syndrome involves complex interactions between cardiovascular, renal, and metabolic conditions.
- Limited data exist on the epidemiology and clinical impact of CKM syndrome in atrial fibrillation (AF) patients.
Purpose of the Study:
- To evaluate the prevalence and impact of CKM domains in a real-world cohort of AF patients.
- To analyze the association between CKM domains, oral anticoagulant (OAC) use, and major adverse outcomes.
Main Methods:
- Analysis of 16,070 AF patients from the GLORIA-AF Registry phase III study.
- CKM domains defined by cardiovascular, renal, and metabolic comorbidities in patients with CHA 2 DS 2 -VASc score ≥ 1.
- Multiple-adjusted regression analyses assessed the association of CKM domains with OAC use and primary composite outcome (all-cause death and major adverse cardiovascular events).
Main Results:
- 12.0% of patients presented with all three CKM domains, showing geographical variation.
- OAC use increased with the number of CKM domains.
- The primary composite outcome incidence rose with increasing CKM domains, particularly in patients with three domains (HR: 1.69). The kidney domain was most associated with clinical outcomes.
Conclusions:
- CKM domains are prevalent and geographically diverse in AF patients.
- CKM syndrome negatively impacts OAC use.
- Increased CKM domain burden is associated with detrimental prognostic effects, including higher risks of all-cause death and MACE.
Background:
Cardio-Kidney-Metabolic (CKM) syndrome results from the complex interaction of cardiovascular, renal and metabolic comorbidities. Data on the epidemiology and clinical impact of the CKM syndrome in patients with atrial fibrillation (AF) are limited. We evaluated CKM domains and their impact in a real-world cohort of patients with AF.
Methods:
From the prospective global GLORIA-AF Registry phase III study, we defined CKM domains according to cardiovascular, renal and metabolic comorbidities or conditions in patients with AF and CHA2DS2-VASc score ≥ 1. We analysed the association of the number and groups of CKM domains with use of oral anticoagulant (OAC) and the risk of major outcomes via multiple-adjusted regression analyses. Our primary outcome was a composite of all-cause death and major adverse cardiovascular events.
Results:
16,070 patients (age 70.1 ± 10.4 years, 45.2% females) were included; 1931 (12.0%) presented with all 3 CKM domains, with substantial geographical variation in the distribution of CKM domains. OAC use increased with the number of CKM domains (Odds Ratio [OR] and 95% Confidence Intervals [CI]: 1.40 [1.14-1.72] and 1.38 [1.07-1.78] for 2 vs. 0 and 3 vs. 0 CKM domains, respectively). Over a 3-year follow-up, the incidence of the primary composite outcome increased with the number of CKM domains, with highest hazard observed in patients with 3 domains (Hazard Ratio [HR] and 95%CI: 1.69 [1.20-2.37]). Among groups of CKM domains, those characterized by the kidney domain showed the highest association with the risk of clinical outcomes.
Conclusions:
In patients with AF, CKM domains are commonly found, and their prevalence is heterogeneous across geographical regions. CKM syndrome influences OAC use and had detrimental prognostic effects, with an increasing risk of all-cause death and MACE as the burden of CKM domains increased.
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