Patients with moderate chronic kidney disease without heart disease have reduced coronary flow velocity reserve

Autor: Gregor Guron, Cecilia Wallentin Guron, Pavlos Kashioulis, Ola Hammarsten, Maria Svensson, Aso Saeed
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Cardio-renal syndrome
medicine.medical_specialty
Heart disease
Heart Diseases
030204 cardiovascular system & hematology
Doppler echocardiography
Left ventricular hypertrophy
Ventricular Function
Left

03 medical and health sciences
Ventricular Dysfunction
Left

0302 clinical medicine
Cardio-Renal Syndrome
Internal medicine
Chronic kidney disease
medicine
Diseases of the circulatory (Cardiovascular) system
Humans
Left atrial volume
Cardiac and Cardiovascular Systems
030212 general & internal medicine
Renal Insufficiency
Chronic

Isovolumetric contraction
Ejection fraction
Kardiologi
medicine.diagnostic_test
business.industry
medicine.disease
Coronary flow velocity reserve
Cross-Sectional Studies
Heart failure
RC666-701
Cardiology
Diastolic dysfunction
Cardio‐renal syndrome
Cardiology and Cardiovascular Medicine
business
Kidney disease
Zdroj: ESC Heart Failure, Vol 7, Iss 5, Pp 2797-2806 (2020)
Popis: AIMS: The overall aim was to identify sub-clinical cardiac abnormalities by echocardiography in patients with chronic kidney disease (CKD) stages 3 and 4 and to investigate underlying mechanisms. METHODS AND RESULTS: Ninety-one patients with CKD stages 3 and 4, without a diagnosis of heart disease, and 41 healthy matched controls were included in this cross-sectional study. Cardiac morphology and function were analysed with Doppler echocardiography and coronary flow velocity reserve (CFVR) in response to adenosine was measured in the left anterior descendent artery to detect coronary microvascular dysfunction (CMD). All study subjects had a left ventricular (LV) ejection fraction > 50%. Patients with CKD showed statistically significant increases in left atrial volume index and transmitral and pulmonary vein flow velocities during atrial contraction and prolonged LV isovolumetric relaxation time. Patients with CKD had significantly reduced CFVR vs. controls (2.74 ± 0.86 vs. 3.40 ± 0.89, P < 0.001), and 43% of patients were classified as having CMD compared with 9% of controls (P = 0.001). CONCLUSIONS: Patients with CKD stages 3 and 4, without a diagnosis of heart disease, showed early abnormalities in LV diastolic function that did not fulfil the criteria for LV dysfunction according to current guidelines. A large proportion of CKD patients had CMD, suggesting that microvascular abnormalities may have a pathogenic role in the development of heart failure in this patient group.
Databáze: OpenAIRE