scholarly journals Reference value of left and right atrial size and phasic function by SSFP CMR at 3.0 T in healthy Chinese adults

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Weihao Li ◽  
Ke Wan ◽  
Yuchi Han ◽  
Hong Liu ◽  
Wei Cheng ◽  
...  
2021 ◽  
Author(s):  
Yiyuan Gao ◽  
Zhen Zhang ◽  
Shanshan Zhou ◽  
Gengxiao Li ◽  
Mingwu Lou ◽  
...  

Abstract The left and right atrial (LA and RA) volumes and function are tightly linked to the morbidity and mortality of multiple cardiovascular diseases. We aimed to establish cardiovascular magnetic resonance (CMR) reference values for LA and RA volumes and phasic function based on a large sample of healthy Chinese adults. 408 validated healthy Chinese adults (54% men; aged 21–70 years) were included. The atrial volumes: maximum, minimum, and pre-atrial contraction (Vmax, Vmin, and Vpac); atrial phasic emptying fractions: total, passive, and booster (EF total, EF passive, and EF booster); atrial phasic emptying volumes: total, passive, and active (TEV, PEV, and AEV); and atrial expansion index (EI) were measured. Normal reference values were calculated and were stratified by sex (men and women) and age decades. The absolute LA and RA volumes and the indexed RA volumes were all greater in men. Women demonstrated higher LAEF total, LAEF booster, LAEI, RAEF total, RAEF passive, RAEF booster, and RAEI, while men had greater RATEV and RAAEV. Aging was positively correlated with the absolute and indexed LA and RA volumes, except for LA Vmax. LA and RA reservoir and conduit function including EF total, EI, EF passive, and PEV increased with age, while the atrial booster function (EF booster and AEV) decreased. We systematically provide age- and sex-specific CMR reference values for LA, RA volumes and phasic function based on a large sample of healthy Chinese adults with a wide age range. Both age and sex are closely associated with atrial volumes and function.


2008 ◽  
Vol 130 (1) ◽  
pp. 69-71 ◽  
Author(s):  
Qiqiong Cui ◽  
Wei Zhang ◽  
Hu Wang ◽  
Xin Sun ◽  
Huanyi Yang ◽  
...  

1993 ◽  
Vol 22 (6) ◽  
pp. 1666-1672 ◽  
Author(s):  
A.T.Marcel Gosselink ◽  
Harry J.G.M. Crijns ◽  
Hans P.M. Hamer ◽  
Hans Hillege ◽  
Kong I. Lie

Author(s):  
M Medvedev, M.V. Kubrina, O.S. Zarubina et all

Two cases of prenatal ultrasound diagnosis of left atrial isomerism in the second trimester of gestation is presented. These two cases were in combination with pulmonary atresia and right aortic arch. Left atrial isomerism was identify by the digit-like shape of the left and right atrial appendages. The pulmonary atresia was identified on the basis of reverse flow in small pulmonary artery. A right aortic was identified by “U”-shaped confluence of aorta and ductus arteriosus in view of three vessels and trachea. The trachea was located between the vessels. The pregnancies were terminated and prenatal diagnosis was conformed at autopsy


2021 ◽  
Author(s):  
Alexandra S Mighiu ◽  
Alice Recalde ◽  
Klemen Ziberna ◽  
Ricardo Carnicer ◽  
Jakub Tomek ◽  
...  

Abstract Aims Gp91-containing NADPH oxidases (NOX2) are a significant source of myocardial superoxide production. An increase in NOX2 activity accompanies atrial fibrillation (AF) induction and electrical remodelling in animal models and predicts incident AF in humans; however, a direct causal role for NOX2 in AF has not been demonstrated. Accordingly, we investigated whether myocardial NOX2 overexpression in mice (NOX2-Tg) is sufficient to generate a favourable substrate for AF and further assessed the effects of atorvastatin, an inhibitor of NOX2, on atrial superoxide production and AF susceptibility. Methods and results NOX2-Tg mice showed a 2- to 2.5-fold higher atrial protein content of NOX2 compared with wild-type (WT) controls, which was associated with a significant (twofold) increase in NADPH-stimulated superoxide production (2-hydroxyethidium by HPLC) in left and right atrial tissue homogenates (P = 0.004 and P = 0.019, respectively). AF susceptibility assessed in vivo by transoesophageal atrial burst stimulation was modestly increased in NOX2-Tg compared with WT (probability of AF induction: 88% vs. 69%, respectively; P = 0.037), in the absence of significant alterations in AF duration, surface ECG parameters, and LV mass or function. Mechanistic studies did not support a role for NOX2 in promoting electrical or structural remodelling, as high-resolution optical mapping of atrial tissues showed no differences in action potential duration and conduction velocity between genotypes. In addition, we did not observe any genotype difference in markers of fibrosis and inflammation, including atrial collagen content and Col1a1, Il-1β, Il-6, and Mcp-1 mRNA. Similarly, NOX2 overexpression did not have consistent effects on RyR2 Ca2+ leak nor did it affect PKA or CaMKII-mediated RyR2 phosphorylation. Finally, treatment with atorvastatin significantly inhibited atrial superoxide production in NOX2-Tg but had no effect on AF induction in either genotype. Conclusion Together, these data indicate that while atrial NOX2 overexpression may contribute to atrial arrhythmogenesis, NOX2-derived superoxide production does not affect the electrical and structural properties of the atrial myocardium.


1999 ◽  
Vol 6 (8) ◽  
pp. 481-486 ◽  
Author(s):  
Matthew J. Budoff ◽  
Songshou Mao ◽  
ShaoJung Wang ◽  
Hamid Bakhsheshi ◽  
Bruce H. Brundage

1982 ◽  
Vol 10 (8) ◽  
pp. 385-390 ◽  
Author(s):  
Gregory P. Fontana ◽  
Jason H. Kirkman ◽  
Thomas G. Disessa ◽  
Arthur D. Hagan ◽  
Satoshi Hiriashi ◽  
...  

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