Oberhänsli I, Mermillod B, Favre H, Friedli B, Girardin E, Paunier L
Clinique de Pédiatrie, Centre d'Informatique Hospitalière, Geneva, Switzerland.
J Am Coll Cardiol. 1990 May;15(6):1438-45. doi: 10.1016/s0735-1097(10)80036-1.
To investigate the alpha-atrial natriuretic factor in congenital cardiac malformations, three groups of children, aged 7 months to 16 years, with different hemodynamic situations were studied during routine cardiac catheterization. Twenty-one (group I) had tetralogy of Fallot, 24 (group II) had a left to right shunt with pulmonary hypertension and 12 (control group) had a minor cardiac lesion. Alpha-atrial natriuretic factor levels were determined by a radioimmunoassay on blood samples from the inferior vena cava, right atrium, pulmonary artery, left atrium and aorta. To evaluate the effect of an acute volume load, measurements of hormone and pressures were repeated after right ventriculography. Alpha-atrial natriuretic factor levels varied over a wide range in all groups and in all chambers investigated. Nevertheless, children with pulmonary hypertension had significantly higher levels of the hormone (p less than 0.01) and were well separated from the control group, but less well from those with tetralogy of Fallot. A 50% increase of alpha-atrial natriuretic factor from the inferior vena cava to the right atrium occurred in patients with shunt lesions with pulmonary hypertension and in patients with tetralogy of Fallot (p less than 0.001) and a further 30% increase from the right atrium to the pulmonary artery (p less than 0.05). After right ventriculography, a 100% to 200% increase of alpha-atrial natriuretic factor was observed in the total sample (p less than 0.001). A positive correlation was observed between right atrial mean pressure and right atrial alpha-atrial natriuretic factor (r = 0.63) and between pulmonary artery mean pressure and pulmonary artery alpha-atrial natriuretic factor (r = 0.61).(ABSTRACT TRUNCATED AT 250 WORDS)
为研究先天性心脏畸形患儿体内的α-心房利钠因子,在常规心导管检查期间,对三组年龄在7个月至16岁、具有不同血流动力学状况的儿童进行了研究。21例(第一组)患有法洛四联症,24例(第二组)有左向右分流伴肺动脉高压,12例(对照组)有轻度心脏病变。通过放射免疫分析法测定下腔静脉、右心房、肺动脉、左心房和主动脉血样中的α-心房利钠因子水平。为评估急性容量负荷的影响,在右心室造影后重复测量激素和压力。在所有研究组和所有腔室中,α-心房利钠因子水平在很宽范围内变化。然而,肺动脉高压患儿的该激素水平显著更高(p<0.01),与对照组有明显区分,但与法洛四联症患儿区分度较小。患有肺动脉高压的分流性病变患儿及法洛四联症患儿,其α-心房利钠因子从下腔静脉到右心房增加50%(p<0.001),从右心房到肺动脉再增加30%(p<0.05)。右心室造影后,整个样本中α-心房利钠因子增加了100%至200%(p<0.001)。观察到右心房平均压与右心房α-心房利钠因子之间呈正相关(r=0.63),肺动脉平均压与肺动脉α-心房利钠因子之间呈正相关(r=0.61)。(摘要截选至250词)