Loading…

Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients

Background Sex difference is related to specific clinical features in PD patients over the disease course. Objectives To investigate the potential sex‐difference effect on the spontaneous neuronal activity within the most reported resting‐state networks in early untreated PD patients and its correla...

Full description

Saved in:
Bibliographic Details
Published in:Movement disorders 2019-07, Vol.34 (7), p.997-1005
Main Authors: De Micco, Rosa, Esposito, Fabrizio, Nardo, Federica, Caiazzo, Giuseppina, Siciliano, Mattia, Russo, Antonio, Cirillo, Mario, Tedeschi, Gioacchino, Tessitore, Alessandro
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43
cites cdi_FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43
container_end_page 1005
container_issue 7
container_start_page 997
container_title Movement disorders
container_volume 34
creator De Micco, Rosa
Esposito, Fabrizio
Nardo, Federica
Caiazzo, Giuseppina
Siciliano, Mattia
Russo, Antonio
Cirillo, Mario
Tedeschi, Gioacchino
Tessitore, Alessandro
description Background Sex difference is related to specific clinical features in PD patients over the disease course. Objectives To investigate the potential sex‐difference effect on the spontaneous neuronal activity within the most reported resting‐state networks in early untreated PD patients and its correlation with baseline and longitudinal clinical features. Methods Fifty‐six drug‐naïve PD patients (30/26 male/female) and 30 (15/15 male/female) matched controls were enrolled in the study. Topological and spectral resting‐state functional MRI features of the sensorimotor, dorsal and ventral attention, frontoparietal, and default‐mode networks were analyzed for possible sex‐difference effects in both PD patients and controls groups. Additionally, a region‐of‐interest analysis was performed to test for a sex effect on basal ganglia connectivity. Multivariate ordinal regression was used to investigate whether connectivity findings at baseline were predictors of motor impairment over a 2‐year follow‐up period. Results Compared to female PD patients and controls, male PD patients showed an abnormal spectral composition of the sensorimotor and dorsal attention networks in the slow‐5 band. The region‐of‐interest analysis showed an increased connectivity within the basal ganglia in female PD patients compared to males. Functional sensorimotor connectivity changes at baseline showed to be an independent predictor of disease severity at 2‐year follow‐up. Conclusions Our findings revealed the presence of a disease‐related, sex‐specific cortical and subcortical connectivity pattern within the sensorimotor network, in the early stage of PD. We hypothesize that these findings may be related to the presence of different sex‐specific nigrostriatal dopaminergic pathways and might predict PD progression. © 2019 International Parkinson and Movement Disorder Society
doi_str_mv 10.1002/mds.27725
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2261278316</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2261278316</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43</originalsourceid><addsrcrecordid>eNp1kMFO3DAQhq2qiN0uHPoCVaQegEPAE8eJfURAaaVFRQLOkeOMK0PibO1kYW99hL4JD9E34UnqZYFDpZ7mMN__aeYn5CPQQ6A0O-qacJiVZcbfkSlwBqnIePmeTKkQPGUg-IR8COGWUgAOxTaZMABBuRRToq_w4enXb4-tGrBJFmoY0LukN4l1g7cuWJ3UXlmX6N451INd2mEVl0njxx8x6dSfxyUml8rfRbp3eyFpbEAVcC2z6IawQ7aMagPuvswZuflydn3yNZ1_P_92cjxPNeOMp5Ibzsomr6VWuaxRA5XIDNSqBAk5o4yB0WBY3uQCeGG00QLj31pIiBE2I_sb78L3P0cMQ9XZoLFtlcN-DFWWFZCVgkER0c__oLf96F28LlJcSsqzci082FDa9yF4NNXC2075VQW0Wjdfxear5-Yj--nFONYdNm_ka9URONoA97bF1f9N1cXp1Ub5F1nWkBM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2259905274</pqid></control><display><type>article</type><title>Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>De Micco, Rosa ; Esposito, Fabrizio ; Nardo, Federica ; Caiazzo, Giuseppina ; Siciliano, Mattia ; Russo, Antonio ; Cirillo, Mario ; Tedeschi, Gioacchino ; Tessitore, Alessandro</creator><creatorcontrib>De Micco, Rosa ; Esposito, Fabrizio ; Nardo, Federica ; Caiazzo, Giuseppina ; Siciliano, Mattia ; Russo, Antonio ; Cirillo, Mario ; Tedeschi, Gioacchino ; Tessitore, Alessandro</creatorcontrib><description>Background Sex difference is related to specific clinical features in PD patients over the disease course. Objectives To investigate the potential sex‐difference effect on the spontaneous neuronal activity within the most reported resting‐state networks in early untreated PD patients and its correlation with baseline and longitudinal clinical features. Methods Fifty‐six drug‐naïve PD patients (30/26 male/female) and 30 (15/15 male/female) matched controls were enrolled in the study. Topological and spectral resting‐state functional MRI features of the sensorimotor, dorsal and ventral attention, frontoparietal, and default‐mode networks were analyzed for possible sex‐difference effects in both PD patients and controls groups. Additionally, a region‐of‐interest analysis was performed to test for a sex effect on basal ganglia connectivity. Multivariate ordinal regression was used to investigate whether connectivity findings at baseline were predictors of motor impairment over a 2‐year follow‐up period. Results Compared to female PD patients and controls, male PD patients showed an abnormal spectral composition of the sensorimotor and dorsal attention networks in the slow‐5 band. The region‐of‐interest analysis showed an increased connectivity within the basal ganglia in female PD patients compared to males. Functional sensorimotor connectivity changes at baseline showed to be an independent predictor of disease severity at 2‐year follow‐up. Conclusions Our findings revealed the presence of a disease‐related, sex‐specific cortical and subcortical connectivity pattern within the sensorimotor network, in the early stage of PD. We hypothesize that these findings may be related to the presence of different sex‐specific nigrostriatal dopaminergic pathways and might predict PD progression. © 2019 International Parkinson and Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.27725</identifier><identifier>PMID: 31180598</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Aged ; Attention - physiology ; Basal ganglia ; Brain - physiopathology ; Brain Mapping - methods ; Cortex ; Dopamine - metabolism ; Dopamine receptors ; drug‐naïve ; Female ; Functional magnetic resonance imaging ; gender ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Middle Aged ; Movement disorders ; MRI ; Neural networks ; Neural Pathways - physiopathology ; Neurodegenerative diseases ; Parkinson Disease - physiopathology ; Parkinson's disease ; resting‐state connectivity ; Sensorimotor system ; Sex ; Sex Factors</subject><ispartof>Movement disorders, 2019-07, Vol.34 (7), p.997-1005</ispartof><rights>2019 International Parkinson and Movement Disorder Society</rights><rights>2019 International Parkinson and Movement Disorder Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43</citedby><cites>FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43</cites><orcidid>0000-0001-5246-2109</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31180598$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Micco, Rosa</creatorcontrib><creatorcontrib>Esposito, Fabrizio</creatorcontrib><creatorcontrib>Nardo, Federica</creatorcontrib><creatorcontrib>Caiazzo, Giuseppina</creatorcontrib><creatorcontrib>Siciliano, Mattia</creatorcontrib><creatorcontrib>Russo, Antonio</creatorcontrib><creatorcontrib>Cirillo, Mario</creatorcontrib><creatorcontrib>Tedeschi, Gioacchino</creatorcontrib><creatorcontrib>Tessitore, Alessandro</creatorcontrib><title>Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients</title><title>Movement disorders</title><addtitle>Mov Disord</addtitle><description>Background Sex difference is related to specific clinical features in PD patients over the disease course. Objectives To investigate the potential sex‐difference effect on the spontaneous neuronal activity within the most reported resting‐state networks in early untreated PD patients and its correlation with baseline and longitudinal clinical features. Methods Fifty‐six drug‐naïve PD patients (30/26 male/female) and 30 (15/15 male/female) matched controls were enrolled in the study. Topological and spectral resting‐state functional MRI features of the sensorimotor, dorsal and ventral attention, frontoparietal, and default‐mode networks were analyzed for possible sex‐difference effects in both PD patients and controls groups. Additionally, a region‐of‐interest analysis was performed to test for a sex effect on basal ganglia connectivity. Multivariate ordinal regression was used to investigate whether connectivity findings at baseline were predictors of motor impairment over a 2‐year follow‐up period. Results Compared to female PD patients and controls, male PD patients showed an abnormal spectral composition of the sensorimotor and dorsal attention networks in the slow‐5 band. The region‐of‐interest analysis showed an increased connectivity within the basal ganglia in female PD patients compared to males. Functional sensorimotor connectivity changes at baseline showed to be an independent predictor of disease severity at 2‐year follow‐up. Conclusions Our findings revealed the presence of a disease‐related, sex‐specific cortical and subcortical connectivity pattern within the sensorimotor network, in the early stage of PD. We hypothesize that these findings may be related to the presence of different sex‐specific nigrostriatal dopaminergic pathways and might predict PD progression. © 2019 International Parkinson and Movement Disorder Society</description><subject>Aged</subject><subject>Attention - physiology</subject><subject>Basal ganglia</subject><subject>Brain - physiopathology</subject><subject>Brain Mapping - methods</subject><subject>Cortex</subject><subject>Dopamine - metabolism</subject><subject>Dopamine receptors</subject><subject>drug‐naïve</subject><subject>Female</subject><subject>Functional magnetic resonance imaging</subject><subject>gender</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Movement disorders</subject><subject>MRI</subject><subject>Neural networks</subject><subject>Neural Pathways - physiopathology</subject><subject>Neurodegenerative diseases</subject><subject>Parkinson Disease - physiopathology</subject><subject>Parkinson's disease</subject><subject>resting‐state connectivity</subject><subject>Sensorimotor system</subject><subject>Sex</subject><subject>Sex Factors</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kMFO3DAQhq2qiN0uHPoCVaQegEPAE8eJfURAaaVFRQLOkeOMK0PibO1kYW99hL4JD9E34UnqZYFDpZ7mMN__aeYn5CPQQ6A0O-qacJiVZcbfkSlwBqnIePmeTKkQPGUg-IR8COGWUgAOxTaZMABBuRRToq_w4enXb4-tGrBJFmoY0LukN4l1g7cuWJ3UXlmX6N451INd2mEVl0njxx8x6dSfxyUml8rfRbp3eyFpbEAVcC2z6IawQ7aMagPuvswZuflydn3yNZ1_P_92cjxPNeOMp5Ibzsomr6VWuaxRA5XIDNSqBAk5o4yB0WBY3uQCeGG00QLj31pIiBE2I_sb78L3P0cMQ9XZoLFtlcN-DFWWFZCVgkER0c__oLf96F28LlJcSsqzci082FDa9yF4NNXC2075VQW0Wjdfxear5-Yj--nFONYdNm_ka9URONoA97bF1f9N1cXp1Ub5F1nWkBM</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>De Micco, Rosa</creator><creator>Esposito, Fabrizio</creator><creator>Nardo, Federica</creator><creator>Caiazzo, Giuseppina</creator><creator>Siciliano, Mattia</creator><creator>Russo, Antonio</creator><creator>Cirillo, Mario</creator><creator>Tedeschi, Gioacchino</creator><creator>Tessitore, Alessandro</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5246-2109</orcidid></search><sort><creationdate>201907</creationdate><title>Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients</title><author>De Micco, Rosa ; Esposito, Fabrizio ; Nardo, Federica ; Caiazzo, Giuseppina ; Siciliano, Mattia ; Russo, Antonio ; Cirillo, Mario ; Tedeschi, Gioacchino ; Tessitore, Alessandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aged</topic><topic>Attention - physiology</topic><topic>Basal ganglia</topic><topic>Brain - physiopathology</topic><topic>Brain Mapping - methods</topic><topic>Cortex</topic><topic>Dopamine - metabolism</topic><topic>Dopamine receptors</topic><topic>drug‐naïve</topic><topic>Female</topic><topic>Functional magnetic resonance imaging</topic><topic>gender</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Movement disorders</topic><topic>MRI</topic><topic>Neural networks</topic><topic>Neural Pathways - physiopathology</topic><topic>Neurodegenerative diseases</topic><topic>Parkinson Disease - physiopathology</topic><topic>Parkinson's disease</topic><topic>resting‐state connectivity</topic><topic>Sensorimotor system</topic><topic>Sex</topic><topic>Sex Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Micco, Rosa</creatorcontrib><creatorcontrib>Esposito, Fabrizio</creatorcontrib><creatorcontrib>Nardo, Federica</creatorcontrib><creatorcontrib>Caiazzo, Giuseppina</creatorcontrib><creatorcontrib>Siciliano, Mattia</creatorcontrib><creatorcontrib>Russo, Antonio</creatorcontrib><creatorcontrib>Cirillo, Mario</creatorcontrib><creatorcontrib>Tedeschi, Gioacchino</creatorcontrib><creatorcontrib>Tessitore, Alessandro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Micco, Rosa</au><au>Esposito, Fabrizio</au><au>Nardo, Federica</au><au>Caiazzo, Giuseppina</au><au>Siciliano, Mattia</au><au>Russo, Antonio</au><au>Cirillo, Mario</au><au>Tedeschi, Gioacchino</au><au>Tessitore, Alessandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov Disord</addtitle><date>2019-07</date><risdate>2019</risdate><volume>34</volume><issue>7</issue><spage>997</spage><epage>1005</epage><pages>997-1005</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>Background Sex difference is related to specific clinical features in PD patients over the disease course. Objectives To investigate the potential sex‐difference effect on the spontaneous neuronal activity within the most reported resting‐state networks in early untreated PD patients and its correlation with baseline and longitudinal clinical features. Methods Fifty‐six drug‐naïve PD patients (30/26 male/female) and 30 (15/15 male/female) matched controls were enrolled in the study. Topological and spectral resting‐state functional MRI features of the sensorimotor, dorsal and ventral attention, frontoparietal, and default‐mode networks were analyzed for possible sex‐difference effects in both PD patients and controls groups. Additionally, a region‐of‐interest analysis was performed to test for a sex effect on basal ganglia connectivity. Multivariate ordinal regression was used to investigate whether connectivity findings at baseline were predictors of motor impairment over a 2‐year follow‐up period. Results Compared to female PD patients and controls, male PD patients showed an abnormal spectral composition of the sensorimotor and dorsal attention networks in the slow‐5 band. The region‐of‐interest analysis showed an increased connectivity within the basal ganglia in female PD patients compared to males. Functional sensorimotor connectivity changes at baseline showed to be an independent predictor of disease severity at 2‐year follow‐up. Conclusions Our findings revealed the presence of a disease‐related, sex‐specific cortical and subcortical connectivity pattern within the sensorimotor network, in the early stage of PD. We hypothesize that these findings may be related to the presence of different sex‐specific nigrostriatal dopaminergic pathways and might predict PD progression. © 2019 International Parkinson and Movement Disorder Society</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>31180598</pmid><doi>10.1002/mds.27725</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5246-2109</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0885-3185
ispartof Movement disorders, 2019-07, Vol.34 (7), p.997-1005
issn 0885-3185
1531-8257
language eng
recordid cdi_proquest_miscellaneous_2261278316
source Wiley-Blackwell Read & Publish Collection
subjects Aged
Attention - physiology
Basal ganglia
Brain - physiopathology
Brain Mapping - methods
Cortex
Dopamine - metabolism
Dopamine receptors
drug‐naïve
Female
Functional magnetic resonance imaging
gender
Humans
Magnetic Resonance Imaging - methods
Male
Middle Aged
Movement disorders
MRI
Neural networks
Neural Pathways - physiopathology
Neurodegenerative diseases
Parkinson Disease - physiopathology
Parkinson's disease
resting‐state connectivity
Sensorimotor system
Sex
Sex Factors
title Sex‐related pattern of intrinsic brain connectivity in drug‐naïve Parkinson's disease patients
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T02%3A45%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sex%E2%80%90related%20pattern%20of%20intrinsic%20brain%20connectivity%20in%20drug%E2%80%90na%C3%AFve%20Parkinson's%20disease%20patients&rft.jtitle=Movement%20disorders&rft.au=De%20Micco,%20Rosa&rft.date=2019-07&rft.volume=34&rft.issue=7&rft.spage=997&rft.epage=1005&rft.pages=997-1005&rft.issn=0885-3185&rft.eissn=1531-8257&rft_id=info:doi/10.1002/mds.27725&rft_dat=%3Cproquest_cross%3E2261278316%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3535-95f537d4b9ca49bec109e3f1ba7191430331fc1f34d48156fcfc8e277c891ca43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2259905274&rft_id=info:pmid/31180598&rfr_iscdi=true