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The Autonomic Nervous System Activity and Aging in Patients with Schizophrenia Mami FUJIBAYASHI 1 , Ikuko KISHIDA 2 , Tetsuya KIMURA 1 , Yosuke YAMADA 1 , Seitaro TANAKA 1 , Chie ISHII 2 , Norio ISHII 2 , Toshio MORITANI 1 1Graduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan 2Seishinkai, Fujisawa Hospital Keyword: Schizophrenia , Autonomic nervous system activity , Heart rate variability , Power spectral analysis , Aging pp.315-323
Published Date 2009/4/15
DOI https://doi.org/10.11477/mf.1405101396
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 Schizophrenia is associated with several chronic physical illnesses and patients with schizophrenia have a shorter life expectancy. These risks may be attributable to altered neural regulation of cardiac autonomic activity. The autonomic nervous system (ANS) modulates the internal environment of human beings, and its activity is known to decrease with age in healthy adults. However, whether or not the activity of the ANS is altered with age in schizophrenia patients remains to be elucidated. The aim of our study is to examine whether heart rate variability (HRV), which is considered to bean indicator of the ANS activity, is altered with aging in schizophrenic patients. A total of 47 schizophrenic patients and 51 healthy controls volunteered to participate in this study. The schizophrenic and healthy individuals were divided into 4 groups according to their ages:people under 40 years, those in their 40s, those in their 50s, and those over 60. The ANS activity was assessed under resting conditions by means of HRV power spectral analysis. In the schizophrenia group, the Global Assessment of Functioning scale was used to evaluate the psychiatric severity, and daily doses of antipsychotics were converted to approximate chlorpromazine equivalents using published guidelines. Significant interactions of age and subject group with respect to the activity of the sympathetic nervous system, parasympathetic nervous system, and the ANS as assessed using two-way ANOVA. The ANS activity was significantly lower in the schizophrenia group (p<0.01) than in the control group. Even the youngest subjects in the schizophrenia group showed significantly lower ANS activity than the oldest subjects in the control group. Several theories have been proposed to explain the underlying mechanisms of schizophrenia and its complex web of biopsychosocial factors. Although the causes and consequences of schizophrenia remain to be elucidated, our findings suggest the possibility that altered function of the ANS in patients with schizophrenia could be associated with not only diverse psychosomatic and behavioral symptoms but also antipsychotic drugs.


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電子版ISSN 1882-126X 印刷版ISSN 0488-1281 医学書院

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