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Correlation between the parameters of contingent negative variation and characteristics of variational pulsometry in Parkinsonian patients
In patients suffering from Parkinson's disease (PD), we analyzed correlations between the parameters of contingent negative variation (CNV) and data of variational pulsometry (according to the measurements of R-R ECG intervals). Studies were carried out on 35 patients (group PD), 49 to 74 years...
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Published in: | Neurophysiology (New York) 2008-05, Vol.40 (3), p.204-214 |
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description | In patients suffering from Parkinson's disease (PD), we analyzed correlations between the parameters of contingent negative variation (CNV) and data of variational pulsometry (according to the measurements of R-R ECG intervals). Studies were carried out on 35 patients (group PD), 49 to 74 years old, with the stage of disease of 1.5 to 3.0 according to the Hoehn-Yahr international classification. In the course of CNV recording (i.e., in the state of a certain functional loading), we observed significant negative correlations between the integral magnitude (area) of this potential and indices of variational pulsometry (RMSSD, SDNN, C. var, and HF) that characterize the intensity of parasympathetic (respiratory) influences on the cardiovascular system. In the control group, such correlations were absent. We found significant correlations between the autonomic balance, CNV magnitude, and stage of PD reflecting the level of generalization of the pathological process. In the subgroup of patients with the PD stage 1.5 to 2.0, significant changes in the mean values of indices of parasympathetic influences during recording of the CNV were not observed, while in another subgroup (the PD stage 2.5 to 3.0), these values increased significantly (
P
< 0.05 and
P
< 0.01). If the estimates of the PD stage were low, the CNV area demonstrated greater values (
P
< 0.01). The disturbance of coordination of muscle-to-muscle interactions in the PD group is, probably, an important factor responsible for parasympathetic dysregulation and suppression of the CNV generation. We found positive correlation between the intensity of parasympathetic influences in the course of CNV recording and the level of postural disorders (
r
= 0.37,
P
< 0.05). On the contrary, the CNV magnitude demonstrated a negative correlation with the intensity of these disorders (
r
= −0.36,
P
< 0.05), as well as with the level of postural instability (
r
= −0.55,
P
< 0.001). We hypothesize that alterations of the autonomic balance and the activity of those cerebral structures, which are responsible for the motor readiness, result, to a significant extent, from weakening of the activity of the noradrenergic system due to degenerative processes developing in cells of the
locus coeruleus
. The impairment of the latter structure, together with degeneration of neurons of the
substantia nigra
and a decrease in the level of nigro-striatal dopamine, underlies the pathomorphological pattern of PD. |
doi_str_mv | 10.1007/s11062-008-9038-z |
format | article |
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P
< 0.05 and
P
< 0.01). If the estimates of the PD stage were low, the CNV area demonstrated greater values (
P
< 0.01). The disturbance of coordination of muscle-to-muscle interactions in the PD group is, probably, an important factor responsible for parasympathetic dysregulation and suppression of the CNV generation. We found positive correlation between the intensity of parasympathetic influences in the course of CNV recording and the level of postural disorders (
r
= 0.37,
P
< 0.05). On the contrary, the CNV magnitude demonstrated a negative correlation with the intensity of these disorders (
r
= −0.36,
P
< 0.05), as well as with the level of postural instability (
r
= −0.55,
P
< 0.001). We hypothesize that alterations of the autonomic balance and the activity of those cerebral structures, which are responsible for the motor readiness, result, to a significant extent, from weakening of the activity of the noradrenergic system due to degenerative processes developing in cells of the
locus coeruleus
. The impairment of the latter structure, together with degeneration of neurons of the
substantia nigra
and a decrease in the level of nigro-striatal dopamine, underlies the pathomorphological pattern of PD.]]></description><identifier>ISSN: 0090-2977</identifier><identifier>EISSN: 1573-9007</identifier><identifier>DOI: 10.1007/s11062-008-9038-z</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Anatomy & physiology ; Biomedical and Life Sciences ; Biomedicine ; Cardiovascular system ; Neurobiology ; Neurons ; Neurosciences ; Parkinson's disease</subject><ispartof>Neurophysiology (New York), 2008-05, Vol.40 (3), p.204-214</ispartof><rights>Springer Science+Business Media, Inc. 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c298t-b02b30442260520faf56ecac143b6c692b86bfdd503e576b21547950dbaa3d123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Lukhanina, E. P.</creatorcontrib><creatorcontrib>Karaban’, I. N.</creatorcontrib><creatorcontrib>Mel’nik, N. A.</creatorcontrib><creatorcontrib>Berezetskaya, N. M.</creatorcontrib><title>Correlation between the parameters of contingent negative variation and characteristics of variational pulsometry in Parkinsonian patients</title><title>Neurophysiology (New York)</title><addtitle>Neurophysiology</addtitle><description><![CDATA[In patients suffering from Parkinson's disease (PD), we analyzed correlations between the parameters of contingent negative variation (CNV) and data of variational pulsometry (according to the measurements of R-R ECG intervals). Studies were carried out on 35 patients (group PD), 49 to 74 years old, with the stage of disease of 1.5 to 3.0 according to the Hoehn-Yahr international classification. In the course of CNV recording (i.e., in the state of a certain functional loading), we observed significant negative correlations between the integral magnitude (area) of this potential and indices of variational pulsometry (RMSSD, SDNN, C. var, and HF) that characterize the intensity of parasympathetic (respiratory) influences on the cardiovascular system. In the control group, such correlations were absent. We found significant correlations between the autonomic balance, CNV magnitude, and stage of PD reflecting the level of generalization of the pathological process. In the subgroup of patients with the PD stage 1.5 to 2.0, significant changes in the mean values of indices of parasympathetic influences during recording of the CNV were not observed, while in another subgroup (the PD stage 2.5 to 3.0), these values increased significantly (
P
< 0.05 and
P
< 0.01). If the estimates of the PD stage were low, the CNV area demonstrated greater values (
P
< 0.01). The disturbance of coordination of muscle-to-muscle interactions in the PD group is, probably, an important factor responsible for parasympathetic dysregulation and suppression of the CNV generation. We found positive correlation between the intensity of parasympathetic influences in the course of CNV recording and the level of postural disorders (
r
= 0.37,
P
< 0.05). On the contrary, the CNV magnitude demonstrated a negative correlation with the intensity of these disorders (
r
= −0.36,
P
< 0.05), as well as with the level of postural instability (
r
= −0.55,
P
< 0.001). We hypothesize that alterations of the autonomic balance and the activity of those cerebral structures, which are responsible for the motor readiness, result, to a significant extent, from weakening of the activity of the noradrenergic system due to degenerative processes developing in cells of the
locus coeruleus
. The impairment of the latter structure, together with degeneration of neurons of the
substantia nigra
and a decrease in the level of nigro-striatal dopamine, underlies the pathomorphological pattern of PD.]]></description><subject>Anatomy & physiology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cardiovascular system</subject><subject>Neurobiology</subject><subject>Neurons</subject><subject>Neurosciences</subject><subject>Parkinson's disease</subject><issn>0090-2977</issn><issn>1573-9007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kctKAzEUhoMoWKsP4C64cDd6kmnmspTiDQRd6DpkMmfa6DSpSaq0j-BTmzqiIJjNIfB9_yH5CTlmcMYAyvPAGBQ8A6iyGvIq2-yQERNlnm5Q7pIRQA0Zr8tynxyE8AwARVWLEfmYOu-xV9E4SxuM74iWxjnSpfJqgRF9oK6j2tlo7AxtpBZniX5D-qa8GTxlW6rnSdCJNyEa_SX9AKqny1UfXMrza2osfVD-xdjgrFE2bYomBYdDstepPuDR9xyTp6vLx-lNdnd_fTu9uMs0r6uYNcCbHCYTzgsQHDrViQK10mySN4Uuat5URdO1rYAcRVk0nIlJWQtoG6XylvF8TE6H3KV3rysMUS5M0Nj3yqJbBclBsDrnZQJP_oDPbuXTaxKTTsWrChLEBkh7F4LHTi69WSi_lgzktho5VCNTNXJbjdwkhw9OSGz6Vf8b_L_0CW4UlYs</recordid><startdate>20080501</startdate><enddate>20080501</enddate><creator>Lukhanina, E. P.</creator><creator>Karaban’, I. N.</creator><creator>Mel’nik, N. A.</creator><creator>Berezetskaya, N. 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P. ; Karaban’, I. N. ; Mel’nik, N. A. ; Berezetskaya, N. M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-b02b30442260520faf56ecac143b6c692b86bfdd503e576b21547950dbaa3d123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Anatomy & physiology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cardiovascular system</topic><topic>Neurobiology</topic><topic>Neurons</topic><topic>Neurosciences</topic><topic>Parkinson's disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lukhanina, E. P.</creatorcontrib><creatorcontrib>Karaban’, I. N.</creatorcontrib><creatorcontrib>Mel’nik, N. A.</creatorcontrib><creatorcontrib>Berezetskaya, N. M.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Neurophysiology (New York)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lukhanina, E. P.</au><au>Karaban’, I. N.</au><au>Mel’nik, N. A.</au><au>Berezetskaya, N. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation between the parameters of contingent negative variation and characteristics of variational pulsometry in Parkinsonian patients</atitle><jtitle>Neurophysiology (New York)</jtitle><stitle>Neurophysiology</stitle><date>2008-05-01</date><risdate>2008</risdate><volume>40</volume><issue>3</issue><spage>204</spage><epage>214</epage><pages>204-214</pages><issn>0090-2977</issn><eissn>1573-9007</eissn><abstract><![CDATA[In patients suffering from Parkinson's disease (PD), we analyzed correlations between the parameters of contingent negative variation (CNV) and data of variational pulsometry (according to the measurements of R-R ECG intervals). Studies were carried out on 35 patients (group PD), 49 to 74 years old, with the stage of disease of 1.5 to 3.0 according to the Hoehn-Yahr international classification. In the course of CNV recording (i.e., in the state of a certain functional loading), we observed significant negative correlations between the integral magnitude (area) of this potential and indices of variational pulsometry (RMSSD, SDNN, C. var, and HF) that characterize the intensity of parasympathetic (respiratory) influences on the cardiovascular system. In the control group, such correlations were absent. We found significant correlations between the autonomic balance, CNV magnitude, and stage of PD reflecting the level of generalization of the pathological process. In the subgroup of patients with the PD stage 1.5 to 2.0, significant changes in the mean values of indices of parasympathetic influences during recording of the CNV were not observed, while in another subgroup (the PD stage 2.5 to 3.0), these values increased significantly (
P
< 0.05 and
P
< 0.01). If the estimates of the PD stage were low, the CNV area demonstrated greater values (
P
< 0.01). The disturbance of coordination of muscle-to-muscle interactions in the PD group is, probably, an important factor responsible for parasympathetic dysregulation and suppression of the CNV generation. We found positive correlation between the intensity of parasympathetic influences in the course of CNV recording and the level of postural disorders (
r
= 0.37,
P
< 0.05). On the contrary, the CNV magnitude demonstrated a negative correlation with the intensity of these disorders (
r
= −0.36,
P
< 0.05), as well as with the level of postural instability (
r
= −0.55,
P
< 0.001). We hypothesize that alterations of the autonomic balance and the activity of those cerebral structures, which are responsible for the motor readiness, result, to a significant extent, from weakening of the activity of the noradrenergic system due to degenerative processes developing in cells of the
locus coeruleus
. The impairment of the latter structure, together with degeneration of neurons of the
substantia nigra
and a decrease in the level of nigro-striatal dopamine, underlies the pathomorphological pattern of PD.]]></abstract><cop>Boston</cop><pub>Springer US</pub><doi>10.1007/s11062-008-9038-z</doi><tpages>11</tpages></addata></record> |
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subjects | Anatomy & physiology Biomedical and Life Sciences Biomedicine Cardiovascular system Neurobiology Neurons Neurosciences Parkinson's disease |
title | Correlation between the parameters of contingent negative variation and characteristics of variational pulsometry in Parkinsonian patients |
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