Purpose: Intraoperative activation sequence mapping during atrial fibrillation (AF) is difficult because of the complexity of the data. The data analysis is time consuming, and picking activation times can be ambiguous. The purpose of this study was to determine whether mapping in the frequency domain during AF can be used to rapidly locate the region and assess the stability of the dominant frequency.
Methods: In 33 patients, epicardial bipolar electrograms were intraoperatively recorded from 250 sites during AF. For each electrogram, a power spectrum was calculated using a fast Fourier transform. The peak frequency below 11 Hz was determined from the power spectrum for each electrogram.
Results: Isofrequency mapping demonstrated that 91% of the patients exhibited a distinct region of maximum (dominant) frequency at least once during the recording period. Nine percent had no distinct region of dominant frequency. A distinct region of stable dominant frequency was located in the left atrium 30% of the time and the right atrium 12% of the time for the entire recording period. The location of dominant frequency changed during the recording period in 48% of the patients. The dominant frequency was highest in patients with chronic AF (8.29 +/- 1.0 Hz) compared to those with paroxysmal AF (PAF) (6.54 +/- 0.62 Hz, P = .001). The dispersion of frequency was higher in the patients with persistent AF (1.03 +/- 0.4 Hz) than in those with PAF (0.6 +/- 0.3 Hz, P < .001).
Conclusion: Frequency mapping rapidly and accurately identifies the region of dominant activation frequency. The frequency is faster and more variable in persistent AF than in PAF. The location of the dominant frequency was unstable, changing during the recording period, in half the patients. The location of the dominant frequency was independent of the type of AF.
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http://dx.doi.org/10.1016/j.jelectrocard.2006.04.009 | DOI Listing |
Cardiovasc Revasc Med
January 2025
Weatherhead PET Imaging Center, Division of Cardiology, Department of Medicine, McGovern Medical School at UTHealth and Memorial Hermann Hospital, Houston, TX, United States of America.
Patients with angina but without obstructive epicardial coronary disease still require a specific mechanistic diagnosis to enable targeted treatment. The overarching term "coronary microvascular dysfunction" (CMD) has been applied broadly - but is it correct? We present a series of case examples culminating a systematic exploration of our large clinical database to distinguish among four categories of coronary pathophysiology. First, by far the largest group of "no stenosis angina" patients exhibits subendocardial ischemia during intact flow through diffuse epicardial disease during dipyridamole vasodilator stress.
View Article and Find Full Text PDFCancer Genet
January 2025
Cincinnati Children's Hospital Medical Center, Division of Oncology, Cincinnati, OH, USA; University of Cincinnati College of Medicine, Cincinnati, OH, USA. Electronic address:
Introduction: POT1 tumor predisposition (POT1-TPD) is an autosomal dominant disorder characterized by increased lifetime malignancy risk. Melanoma, angiosarcoma, and chronic lymphocytic leukemia are the most frequently reported malignancies [1]. Protection of telomeres protein 1 (POT1) is part of the shelterin protein complex to maintain/protect telomeres [2].
View Article and Find Full Text PDFMethods Cell Biol
January 2025
State University of Minas Gerais, Department of Biomedical Sciences and Health, Passos, MG, Brazil. Electronic address:
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder characterized by a repeat of the cytosine-adenine-guanine trinucleotide (CAG) in the huntingtin gene (HTT). This results in the translation of a mutant huntingtin (mHTT) protein with an abnormally long polyglutamine (polyQ) repeat. The pathology of HD leads to neuronal cell loss, motor abnormalities, and dementia.
View Article and Find Full Text PDFHum Immunol
January 2025
The Second Affiliated Hospital of Guangxi Medical University, Department of Nephrology, Nanning, Guangxi 530021, China. Electronic address:
Background: Microscopic polyangiitis (MPA) is a severe multisystem autoimmune disease featured by small-vessel vasculitis with few or no immune complex, also has a significant genetic predisposition. Growing evidence has confirmed that STAT4 gene is tightly associated with multiple autoimmune diseases, but its contribution to MPA onset is still elusive.
Objective: The aim was to investigated the association between STAT4 gene polymorphisms (rs7572482, rs7574865 and rs12991409) and MPA susceptibility in a Guangxi population of China.
Viruses
January 2025
Global Health Program, Washington State University Global Health-Kenya, Nairobi 00200, Kenya.
Human outbreaks of Middle East respiratory syndrome coronavirus (MERS-CoV) are more common in Middle Eastern and Asian human populations, associated with clades A and B. In Africa, where clade C is dominant in camels, human cases are minimal. We reviewed 16 studies (n = 6198) published across seven African countries between 2012 and 2024 to assess human MERS-CoV cases.
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