Lyme disease (LD), caused by , is a tick-borne illness that can lead to Lyme carditis, which most commonly presents as a high-degree atrioventricular (AV) block. While conduction abnormalities are well-documented, LD has also been implicated in non-ischemic cardiomyopathy, though this manifestation remains rare and under-recognized. We present the case of a 57-year-old female with newly diagnosed heart failure with reduced ejection fraction (HFrEF) and first-degree AV block, who initially presented with nausea, dizziness, fatigue, and gastrointestinal symptoms. Her history included multiple tick bites, subacute joint pain, and intermittent nonspecific rashes. Initial transthoracic echocardiography (TTE) demonstrated severe global hypokinesis with a left ventricular ejection fraction (LVEF) of 10-15%. Extensive ischemic and inflammatory workups, including coronary angiography and cardiac MRI, were unremarkable. However, Lyme serology was positive, and the patient was started on a 21-day course of doxycycline alongside guideline-directed heart failure therapy. A follow-up TTE months later demonstrated remarkable recovery, with LVEF improving to 55-59% and resolution of wall motion abnormalities. This case highlights the importance of considering LD as a reversible cause of non-ischemic cardiomyopathy, particularly in patients with risk factors such as tick exposure and relevant clinical symptoms. Early recognition and appropriate antimicrobial treatment can lead to significant cardiac recovery, underscoring the need for a high index of suspicion when evaluating new-onset systolic dysfunction with an otherwise negative ischemic workup.
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http://dx.doi.org/10.7759/cureus.78770 | DOI Listing |
Cureus
February 2025
Internal Medicine, University of Florida College of Medicine, Gainesville, USA.
Lyme disease (LD), caused by , is a tick-borne illness that can lead to Lyme carditis, which most commonly presents as a high-degree atrioventricular (AV) block. While conduction abnormalities are well-documented, LD has also been implicated in non-ischemic cardiomyopathy, though this manifestation remains rare and under-recognized. We present the case of a 57-year-old female with newly diagnosed heart failure with reduced ejection fraction (HFrEF) and first-degree AV block, who initially presented with nausea, dizziness, fatigue, and gastrointestinal symptoms.
View Article and Find Full Text PDFEur J Hum Genet
March 2025
Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.
Pathogenic variants in the EMD gene cause X-linked Emery-Dreifuss muscular dystrophy type 1 (EDMD1), typically presenting with joint contractures and skeletal muscle atrophy, followed by atrial arrhythmias, cardiac conduction defects, and atrial dilatation. Although an association with isolated dilated cardiomyopathy (DCM) has been suggested, evidence is currently insufficient to verify the gene-disease association. We investigated the causality of a missense variant, c.
View Article and Find Full Text PDFAnn Cardiol Angeiol (Paris)
March 2025
Cardiologie, Centre Hospitalier de Mouscron, Avenue de Fécamp 49, 7700 Mouscron, Belgique.
Left ventricular thrombus (LVT) is a serious complication of both ischemic and non-ischemic cardiomyopathies, with a high risk of morbidity and mortality due to systemic embolism. We present the case of a 73-year-old man with a history of myocardial infarction who subsequently developed an apical thrombus. Seven years after the initial event, this thrombus caused a splenic infarction complicated by an abscessed hematoma.
View Article and Find Full Text PDFJ Interv Card Electrophysiol
March 2025
Division of Cardiology, University of Washington, 1959 NE Pacific St, Seattle, WA, 98195, USA.
Background: Cardiomyopathy (CM) is associated with atrial remodeling and atrial fibrillation (AF), often complicating rhythm management. Ventricular dysfunction contributes to AF through pressure and volume overload, while AF worsens ventricular function via tachycardia and irregular activation. Evidence suggests catheter ablation improves outcomes in CM patients, though success is influenced by the extent of atrial and ventricular remodeling.
View Article and Find Full Text PDFCardiol Res
April 2025
Division of Cardiology, Department of Internal Medicine, St. Louis University Hospital, St. Louis, MO, USA.
Background: We sought to compare the long-term outcomes in patients with transthyretin cardiac amyloidosis (CA) compared to those with non-ischemic cardiomyopathy (NICM) from a large healthcare system database.
Methods: Patients with CA or NICM were identified from SSM Healthcare System's data warehouse using ICD codes. Inclusion criteria included at least 6 months of follow-up.
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