Cardiac repolarization evolves differently during the course of benign and disabling multiple sclerosis

被引:3
作者
Mikkola, Alma [1 ,2 ]
Ojanen, Aku [3 ,9 ]
Hartikainen, Juha E. K. [4 ,5 ]
Remes, Anne M. [1 ,2 ,6 ,7 ,10 ,11 ]
Simula, Sakari [8 ,9 ]
机构
[1] Kuopio Univ Hosp, Dept Neurol, Kuopio, Finland
[2] Univ Eastern Finland, Inst Clin Med Neurol, Canthia Bldg,POB 1627, Kuopio 70211, Finland
[3] Mikkeli Cent Hosp, Dept Clin Physiol & Nucl Med, Mikkeli, Finland
[4] Kuopio Univ Hosp, Heart Ctr, POB 100, Kuopio 70029, Finland
[5] Univ Eastern Finland, Inst Clin Med Med, Kuopio, Finland
[6] Oulu Univ Hosp, Med Res Ctr, Oulu, Finland
[7] Univ Oulu, Res Unit Clin Neurosci, Neurol, Oulu, Finland
[8] Mikkeli Cent Hosp, Dept Neurol, Mikkeli, Finland
[9] Porrassalmenkatu 35-37, Mikkeli 50100, Finland
[10] OUH, POB 20, Oulu 90029, Finland
[11] OU, POB 5000, Oulu 90014, Finland
关键词
Relapsing-remitting multiple sclerosis; RRMS; Cardiac repolarization; QTc; Heart rate; Autonomic nervous system; AUTONOMIC NERVOUS-SYSTEM; QT INTERVAL; DEATH; DISABILITY; MORTALITY; SURVIVAL; ATROPHY;
D O I
10.1016/j.msard.2018.01.029
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Cardiac repolarization is modulated by the autonomic nervous system. Even though multiple sclerosis associates with prolonged cardiac repolarization the physiology responsible for the phenomenon remains unknown. Objective: To study in longitudinal setting whether the patients with confirmed benign and disabling outcome of relapsing-remitting multiple sclerosis (RRMS) differ in regard to changes of cardiac repolarization. Methods: Total of 43 patients, 26% with benign (EDSS <= 2 at least 10y after onset symptom) and 74% with disabling (EDSS > 2 at least 10y after onset symptom) RRMS, having 12-lead electrocardiogram (ECG) recorded at the time of onset symptom (ECG1) and for follow-up (ECG2), were studied. Heart rate (HR) corrected QT intervals (QTc) reflecting cardiac repolarization were assessed. Results: The time interval between ECG1 and ECG2 showed no statistical difference between benign (7.8 +/- 4.8y) and disabling (10.2 +/- 5.6y; p=. 211) RRMS. Patients with benign and disabling RRMS showed similar values of HR (66 +/- 9 bpm vs 73 +/- 15 bpm; p=.146) and QTc (403 +/- 13 ms vs 408 +/- 19 ms; p=.450) at the time of ECG1. However, at the time of ECG2, HR was higher (79 +/- 14 bpm vs 65 +/- 10 bpm; p=.004) and QTc was longer (420 +/- 24 ms vs 400 +/- 15 ms; p=.012) in patients with disabling than benign RRMS. Correspondingly, HR increased (p=.063) and QTc prolonged (p=.014) during the disease course only in patients with disabling RRMS. Conclusions: Deterioration of cardiac autonomic regulation during the disease course associates with disabling but not with benign RRMS. Our findings suggest that assessment of cardiac autonomic regulation should be included in the evaluation of RRMS disease course. In addition, patients with disabling RRMS might be prone to unfavorable cardiovascular outcome also due to deterioration of autonomic nervous system.
引用
收藏
页码:205 / 209
页数:5
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