The effect of angiotensin-converting enzyme polymorphism on hemodynamic response to endotracheal intubation in hypertensive patients

• Published in: Scandinavian journal of clinical and laboratory investigation Vol. 76; no. 5; pp. 368 - 372
• Main Authors: Wang, Jun, Wang, Zhi-Ping, Wang, Hao-Xing, Shao, Mu-Qing, Mu, Hui-Jun
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis 03.07.2016
• Subjects: Aged; Anesthesia; Angiotensin converting enzyme gene; Blood Pressure; Catecholamines - blood; Female; Hemodynamics; Humans; hypertension; Hypertension - blood; Hypertension - enzymology; Hypertension - physiopathology; intratracheal complications; intubation; Intubation, Intratracheal - adverse effects; Male; Middle Aged; Myocardial Ischemia - etiology; Myocardial Ischemia - genetics; Peptidyl-Dipeptidase A - blood; Peptidyl-Dipeptidase A - genetics; Polymorphism, Genetic; intubation; Angiotensin converting enzyme gene; hypertension; intratracheal complications
• ISSN: 0036-5513; 1502-7686
• DOI: 10.1080/00365513.2016.1183259

Endotracheal intubation elicits a hemodynamic response associated with increased heart rate and blood pressure that is influenced by the angiotensin-converting enzyme (ACE) insertion (I)/deletion (D) genetic polymorphism which may be of importance also for the pressure response to anesthesia. A total of 337 patients underwent abdominal surgery in general anesthesia and 16% were D/D-homozygotes, 45% were I/D heterozygotes and 39% of the patients were I/I homozygotes. Before surgery most patients were in treatment for arterial hypertension. Systolic and diastolic pressure, heart rate and concentrations of catecholamines in blood were determined before and after induction of anesthesia and for up to 10 minutes following endotracheal intubation. Anesthesia decreased blood pressure and for patients presenting ID and DD, blood pressure and heart rate reached similar levels but compared to II-homozygotes, D-carriers demonstrated significantly higher levels for systolic pressure and heart rate before and after intubation (p < 0.05). The blood levels of catercholamines were similar in the three genotype groups. The incidence of ECG-determined myocardial ischemia was higher in D-allele carriers compared to I-allele homozygotes (DD 22%, ID 25% vs. II 5%). In response to anesthesia and intubation and independent of sympathetic nervous activity, D-allele carriers for ACE polymorphism increased blood pressure response and higher risk for development of cardiovascular complications compared to patients homozygous for the I-allele.