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1.
PLoS One ; 18(5): e0283762, 2023.
Artículo en Inglés | MEDLINE | ID: covidwho-20238524

RESUMEN

The isolating nature of various COVID-19 mandates may have reduced physical activity (PA) and increased mental health symptomology among individuals with amputation. However, an investigation of mental health across PA levels before and after the onset of COVID-19 among this group has not been conducted. Therefore, the objective of this study was to investigate group differences in depression, anxiety, and post-traumatic stress symptomology among individuals with amputation who reported being physically "active," "somewhat active," or "inactivate" before and during the pandemic. Individuals with an amputation at any level (n = 91; 51% female; age = 52.5±15.5) completed an online questionnaire to assess demographic information, PA levels, and mental health throughout the pandemic. Group differences in self-reported PA before and after COVID-19 onset were assessed by the PA Guidelines for Americans recommendations. The Center for Epidemiologic Studies Depression Scale (CES-D), Generalized Anxiety Disorder (GAD-7), and Posttraumatic Stress Disorder Checklist (PCL-5) scales were used to assess group differences in mental health status. Before and after the onset of COVID-19, 33% and 42.9% of respondents reported that they were inactive, respectively. 58.2% of respondents reported decreased PA since the pandemic's onset. Prior to the pandemic, active individuals reported lower CES-D (14.21 vs. 19.07; Cohen's d: -0.414), GAD-7 (3.82 vs. 5.47; Cohen's d: -0.359), and PCL-5 (15.92 vs. 21.03; Cohen's d: -0.319) scores compared to inactive individuals. After the onset of COVID-19, scores remained lower for active respondents CES-D (12.67 vs. 20.03; Cohen's d: 0.-669), GAD-7 (3.17 vs. 5.87; Cohen's d: -0.598), and PCL-5 (13.39 vs. 19.90; Cohen's d: -0.430). Individuals with amputation reported decreased PA after the onset of COVID-19. Individuals reporting that they were "active" exhibited improved depression and anxiety symptomology scores compared to those reporting that they were "inactive."


Asunto(s)
COVID-19 , Salud Mental , Humanos , Femenino , Adulto , Persona de Mediana Edad , Anciano , Masculino , Pandemias , COVID-19/epidemiología , Ejercicio Físico , Ansiedad/epidemiología , Amputación Quirúrgica , Depresión/epidemiología
2.
Am J Hypertens ; 35(11): 948-954, 2022 Nov 02.
Artículo en Inglés | MEDLINE | ID: covidwho-2097304

RESUMEN

BACKGROUND: Although hypertension is a risk factor for severe Coronavirus Disease 2019 (COVID-19) illness, little is known about the effects of COVID-19 on blood pressure (BP). Central BP measures taken over a 24-hour period using ambulatory blood pressure monitoring (ABPM) adds prognostic value in assessing cardiovascular disease (CVD) risk compared with brachial BP measures from a single time point. We assessed CVD risk between adults with and without a history of COVID-19 via appraisal of 24-hour brachial and central hemodynamic load from ABPM. METHODS: Cross-sectional analysis was performed on 32 adults who tested positive for COVID-19 (29 ± 13 years, 22 females) and 43 controls (28 ± 12 years, 26 females). Measures of 24-hour hemodynamic load included brachial and central systolic and diastolic BP, pulse pressure, augmentation index (AIx), pulse wave velocity (PWV), nocturnal BP dipping, the ambulatory arterial stiffness index (AASI), and the blood pressure variability ratio (BPVR). RESULTS: Participants who tested positive for COVID-19 experienced 6 ± 4 COVID-19 symptoms, were studied 122 ± 123 days after testing positive, and had mild-to-moderate COVID-19 illness. The results from independent samples t-tests showed no significant differences in 24-hour, daytime, or nighttime measures of central or peripheral hemodynamic load across those with and without a history of COVID-19 (P > 0.05 for all). CONCLUSIONS: No differences in 24-hour brachial or central ABPM measures were detected between adults recovering from mild-to-moderate COVID-19 and controls without a history of COVID-19. Adults recovering from mild-to-moderate COVID-19 do not have increased 24-hour central hemodynamic load.


Asunto(s)
COVID-19 , Hipertensión , Rigidez Vascular , Adulto , Femenino , Humanos , Monitoreo Ambulatorio de la Presión Arterial/métodos , Análisis de la Onda del Pulso/métodos , Estudios Transversales , Presión Sanguínea , Rigidez Vascular/fisiología , Hemodinámica
3.
J Cardiopulm Rehabil Prev ; 41(3): 199-201, 2021 05 01.
Artículo en Inglés | MEDLINE | ID: covidwho-1072449

RESUMEN

INTRODUCTION: Both inflammation and cardiorespiratory fitness (CRF) are associated with the risk of respiratory infections. To clarify the hypothesis that CRF attenuates the incident risk of pneumonia due to inflammation, we conducted a prospective study examining the independent and joint associations of inflammation and CRF on the risk of pneumonia in a population sample of 2041 middle-aged men. METHODS: Cardiorespiratory fitness was directly measured as peak oxygen uptake (V˙o2peak) during progressive exercise testing to volitional fatigue, and categorized into tertiles. Inflammation was defined by high-sensitivity C-reactive protein (hsCRP). Pneumonia cases were identified by internal medicine physicians using the International Classification of Diseases codes in clinical practice. RESULTS: During a median follow-up of 27 yr, 432 pneumonia cases were recorded. High hsCRP and CRF were associated with a higher risk (HR = 1.38; 95% CI, 1.02-1.88) and a lower risk of pneumonia (HR = 0.55; CI, 0.39-0.76) after adjusting for potential confounders, respectively. Compared with normal hsCRP-Fit, moderate to high hsCRP-Unfit had an increased risk of pneumonia (HR = 1.63; CI, 1.21-2.20), but moderate to high hsCRP-Fit was not associated with an increased risk of pneumonia (HR = 1.25; CI, 0.93-1.68). CONCLUSIONS: High CRF attenuates the increased risk of pneumonia due to inflammation. These findings have potential implications for the prevention of respiratory infection characterized by systemic inflammation, such as coronavirus disease-2019 (COVID-19).


Asunto(s)
Capacidad Cardiovascular/fisiología , Inflamación/epidemiología , Inflamación/fisiopatología , Neumonía/epidemiología , Neumonía/fisiopatología , Adulto , Proteína C-Reactiva/metabolismo , Causalidad , Estudios de Cohortes , Comorbilidad , Prueba de Esfuerzo , Finlandia/epidemiología , Estudios de Seguimiento , Humanos , Incidencia , Inflamación/sangre , Masculino , Persona de Mediana Edad , Neumonía/sangre , Estudios Prospectivos , Factores de Riesgo
4.
Med Hypotheses ; 143: 110197, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: covidwho-716873

RESUMEN

Coronavirus disease 2019 (COVID-19) may have a metabolic origin given strong links with risk factors such as lipids and glucose and co-morbidities such as obesity and type 2 diabetes mellitus. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein mediates viral cellular entry via the ACE2 receptor. The cytoplasmic tail of this spike protein is heavily palmitoylated. Emerging studies suggest that SARS-CoV-2 alters lipid metabolism in the lung epithelial cells by modulating peroxisome proliferator-activated receptor alpha (PPARα), possibly contributing to lipotoxicity, inflammation and untoward respiratory effects. Disruption of this process may affect palmitoylation of SARS-CoV spike protein and thus infectivity and viral assembly. COVID-19 is also increasingly being recognized as a vascular disease, with several studies noting prominent systemic endothelial dysfunction. The pathogenesis of endothelial dysfunction may also be linked to COVID-19-mediated metabolic and inflammatory effects. Herein, exercise will be compared to fenofibrate as a possible therapeutic strategy to bolster resilience against (and help manage recovery from) COVID-19. This paper will explore the hypothesis that exercise may be a useful adjuvant in a setting of COVID-19 management/rehabilitation due to its effects on PPARα and vascular endothelial function.


Asunto(s)
Infecciones por Coronavirus/terapia , Terapia por Ejercicio/métodos , PPAR alfa/metabolismo , Neumonía Viral/terapia , Glicoproteína de la Espiga del Coronavirus/metabolismo , Betacoronavirus , COVID-19 , Comorbilidad , Infecciones por Coronavirus/tratamiento farmacológico , Citoplasma/metabolismo , Diabetes Mellitus Tipo 2/complicaciones , Ejercicio Físico , Fenofibrato/química , Humanos , Inflamación , Metabolismo de los Lípidos , Lipoilación , Pulmón/metabolismo , Obesidad/complicaciones , Pandemias , SARS-CoV-2 , Tratamiento Farmacológico de COVID-19
5.
JAMA Cardiol ; 5(10): 1198, 2020 10 01.
Artículo en Inglés | MEDLINE | ID: covidwho-636343
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