Impact of family history of coronary artery disease on clinical outcomes in Takotsubo cardiomyopathy

Author:

Li Pengyang1,Jin Chengyue2,Cui Can3,Cai Peng4,Manohar Shamita Alisa1,Jin Ling5,Wei Xin1,Pan Su6,Dixon Richard A F6,Liu Qi6ORCID

Affiliation:

1. Division of Cardiology, Pauley Heart Center, Virginia Commonwealth University, Richmond, Virginia, USA

2. Department of Medicine, Westchester Medical Center, Valhalla, New York, USA

3. Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA

4. Department of Mathematical Sciences, Worcester Polytechnic Institute, Worcester, Massachusetts, USA

5. Department of Medicine, Metrowest Medical Center, Framingham, Massachusetts, USA

6. Wafic Said Molecular Cardiology Research Laboratory, Texas Heart Institute, Houston, Texas, USA

Abstract

Family history of coronary artery disease (FHxCAD) is a critical risk factor for CAD, underscoring the contribution of genetic factors to disease pathogenesis and susceptibility. Takotsubo cardiomyopathy (TCM) simulates the clinical features of and frequently coexists with CAD. However, the association between FHxCAD and TCM is unclear. Here, we retrospectively examined the impact of FHxCAD on in-hospital outcomes of patients with TCM. Using the National Inpatient Sample database (2016–2018), we identified 4733 patients admitted to hospital with a primary diagnosis of TCM. We compared in-hospital outcomes and complications between TCM patients with (n=646, 13.7%) and without FHxCAD (n=646) in the unmatched and in a propensity-score matched cohort (1:1 ratio). TCM with FHxCAD patients had a reduced incidence of cardiogenic shock, acute kidney injury (AKI), and acute respiratory failure (ARF); lower mortality rates; shorter length of stay (LOS); and decreased total charge compared with TCM without FHxCAD patients (p<0.05). In the matched cohort, TCM with FHxCAD patients (vs TCM without FHxCAD patients) had a lower incidence of cardiogenic shock (2.2% vs 6.3%, p<0.001; OR 0.33, 95% CI 0.18 to 0.61), AKI (5.1% vs 8.7%, p=0.016; OR 0.57, 95% CI 0.36 to 0.88), and ARF (5.7% vs 12.7%, p<0.001; OR 0.42, 95% CI 0.28 to 0.63); decreased in-hospital mortality (<11% vs 3.1%, p=0.002; OR 0.2, 95% CI 0.07 to 0.57); shorter LOS (2.66±1.96 days vs 3.40±3.05 days, p<0.001); and a reduced total charge (p=0.001), respectively. FHxCAD was associated with favorable outcomes in both unmatched and propensity-matched cohorts.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

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