miR Profile of Chronic Right Ventricular Pacing: a Pilot Study in Children with Congenital Complete Atrioventricular Block

被引:1
作者
Navarre, Brittany M. [1 ]
Clouthier, Katie L. [1 ]
Ji, Xuhuai [2 ,3 ]
Taylor, Anne [1 ]
Weldy, Chad S. [4 ]
Dubin, Anne M. [1 ]
Reddy, Sushma [1 ,5 ]
机构
[1] Stanford Univ, Lucile Packard Childrens Hosp, Dept Pediat Cardiol, 750 Welch Rd,Suite 325, Stanford, CA 94304 USA
[2] Stanford Univ, Human Immune Monitoring Ctr, Stanford, CA 94305 USA
[3] Stanford Univ, Funct Genom Facil, Stanford, CA 94305 USA
[4] Stanford Univ, Stanford Med Ctr, Dept Med Cardiovasc, 300 Pasteur Dr, Stanford, CA 94305 USA
[5] Stanford Univ, Cardiovasc Inst, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
MicroRNA; Pacing; Children; Remodeling; Heart failure; COMPLETE HEART-BLOCK; DILATED CARDIOMYOPATHY; MYOCARDIAL-PERFUSION; FAILURE; EXPRESSION; MICRORNAS; MECHANISMS; DISEASES;
D O I
10.1007/s12265-022-10318-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic ventricular pacing can lead to pacing-induced cardiomyopathy (PICM). Clinical data alone is insufficient to predict who will develop PICM. Our study aimed to evaluate the circulating miR profile associated with chronic right ventricular pacing in children with congenital complete AV block (CCAVB) and to identify candidate miRs for longitudinal monitoring. Clinical data and blood were collected from chronically paced children (N= 9) and compared with non-paced controls (N = 13). miR microarrays from the huffy coat revealed 488 differentially regulated miRs between groups. Pathway analysis predicted both adaptive and maladaptive miR signaling associated with chronic pacing despite preserved ventricular function. Greater profibrotic signaling (miRs-92a, 130, 27, 29) and sodium and calcium channel dysregulation (let-7) were seen in those paced > 10 years with the most dyregulation seen in a patient with sudden death vs. those paced < 10 years. These miRs may help to identify early adverse remodeling in this population.
引用
收藏
页码:287 / 299
页数:13
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