A mechanism for immediate reduction in mitral regurgitation after Cardiac resynchronization therapy: Insights from mechanical activation strain mapping

We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping. Heart failure patients w...

Full description

Saved in:
Bibliographic Details
Published inJournal of the American College of Cardiology Vol. 44; no. 8; pp. 1619 - 1625
Main Authors KANZAKI, Hideaki, BAZAZ, Raveen, SCHWARTZMAN, David, DOHI, Kaoru, SADE, L. Elif, GORCSAN, John III
Format Journal Article
LanguageEnglish
Published New York, NY Elsevier Science 19.10.2004
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0735-1097
1558-3597
DOI10.1016/j.jacc.2004.07.036

Cover

Abstract We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping. Heart failure patients with left bundle branch block often benefit acutely from CRT; however, the role and mechanism of reduction of MR are unclear. Twenty-six consecutive patients undergoing CRT with at least mild MR were studied (ejection fraction 24 +/- 6%; QRS duration 168 +/- 30 ms). Echocardiographic Doppler and strain imaging was performed immediately before and the day after CRT, as well as in 10 normal control subjects. Mechanical activation sequence maps were constructed using longitudinal strain from 12 basal and mid-LV sites, with color coding of time-to-peak strain. Mitral regurgitation by the volumetric method consistently decreased after CRT: regurgitant volume from 40 +/- 20 ml to 24 +/- 17 ml and regurgitant fraction from 40 +/- 12% to 25 +/- 14% (both: p < 0.001 vs. baseline). Normal controls had uniform segmental time-to-peak strain, with a difference of only 12 +/- 8 ms between all segments. In contrast, CRT patients at baseline had a 106 +/- 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal). This interpapillary muscle time delay shortened after CRT to 39 +/- 43 ms (p < 0.001 vs. baseline) and was significantly correlated with reductions in mitral regurgitant fraction (r = 0.77, p < 0.001). Cardiac resynchronization therapy significantly and immediately reduced MR. Improved coordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechanistic contributor to immediate MR reduction by CRT.
AbstractList We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping. Heart failure patients with left bundle branch block often benefit acutely from CRT; however, the role and mechanism of reduction of MR are unclear. Twenty-six consecutive patients undergoing CRT with at least mild MR were studied (ejection fraction 24 +/- 6%; QRS duration 168 +/- 30 ms). Echocardiographic Doppler and strain imaging was performed immediately before and the day after CRT, as well as in 10 normal control subjects. Mechanical activation sequence maps were constructed using longitudinal strain from 12 basal and mid-LV sites, with color coding of time-to-peak strain. Mitral regurgitation by the volumetric method consistently decreased after CRT: regurgitant volume from 40 +/- 20 ml to 24 +/- 17 ml and regurgitant fraction from 40 +/- 12% to 25 +/- 14% (both: p < 0.001 vs. baseline). Normal controls had uniform segmental time-to-peak strain, with a difference of only 12 +/- 8 ms between all segments. In contrast, CRT patients at baseline had a 106 +/- 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal). This interpapillary muscle time delay shortened after CRT to 39 +/- 43 ms (p < 0.001 vs. baseline) and was significantly correlated with reductions in mitral regurgitant fraction (r = 0.77, p < 0.001). Cardiac resynchronization therapy significantly and immediately reduced MR. Improved coordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechanistic contributor to immediate MR reduction by CRT.
Objectives We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping. Background Heart failure patients with left bundle branch block often benefit acutely from CRT; however, the role and mechanism of reduction of MR are unclear. Methods Twenty-six consecutive patients undergoing CRT with at least mild MR were studied (ejection fraction 24 ± 6%; QRS duration 168 ± 30 ms). Echocardiographic Doppler and strain imaging was performed immediately before and the day after CRT, as well as in 10 normal control subjects. Mechanical activation sequence maps were constructed using longitudinal strain from 12 basal and mid-LV sites, with color codingof time-to-peak strain. Results Mitral regurgitation by the volumetric method consistently decreased after CRT: regurgitant volume from 40 ± 20 ml to 24 ± 17 ml and regurgitant fraction from 40 ± 12% to 25 ± 14% (both: p < 0.001 vs. baseline). Normal controls had uniform segmental time-to-peak strain, with a difference of only 12 ± 8 ms between all segments. In contrast, CRT patients at baseline had a 106 ± 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal). This interpapillary muscle time delay shortened after CRT to 39 ± 43 ms (p < 0.001 vs. baseline) and was significantly correlated with reductions in mitral regurgitant fraction (r = 0.77, p < 0.001). Conclusions Cardiac resynchronization therapy significantly and immediately reduced MR. Improved coordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechanistic contributor to immediate MR reduction by CRT.
We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping.OBJECTIVESWe tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved coordinated timing of the papillary muscle insertion sites, using the novel approach of mechanical activation strain mapping.Heart failure patients with left bundle branch block often benefit acutely from CRT; however, the role and mechanism of reduction of MR are unclear.BACKGROUNDHeart failure patients with left bundle branch block often benefit acutely from CRT; however, the role and mechanism of reduction of MR are unclear.Twenty-six consecutive patients undergoing CRT with at least mild MR were studied (ejection fraction 24 +/- 6%; QRS duration 168 +/- 30 ms). Echocardiographic Doppler and strain imaging was performed immediately before and the day after CRT, as well as in 10 normal control subjects. Mechanical activation sequence maps were constructed using longitudinal strain from 12 basal and mid-LV sites, with color coding of time-to-peak strain.METHODSTwenty-six consecutive patients undergoing CRT with at least mild MR were studied (ejection fraction 24 +/- 6%; QRS duration 168 +/- 30 ms). Echocardiographic Doppler and strain imaging was performed immediately before and the day after CRT, as well as in 10 normal control subjects. Mechanical activation sequence maps were constructed using longitudinal strain from 12 basal and mid-LV sites, with color coding of time-to-peak strain.Mitral regurgitation by the volumetric method consistently decreased after CRT: regurgitant volume from 40 +/- 20 ml to 24 +/- 17 ml and regurgitant fraction from 40 +/- 12% to 25 +/- 14% (both: p < 0.001 vs. baseline). Normal controls had uniform segmental time-to-peak strain, with a difference of only 12 +/- 8 ms between all segments. In contrast, CRT patients at baseline had a 106 +/- 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal). This interpapillary muscle time delay shortened after CRT to 39 +/- 43 ms (p < 0.001 vs. baseline) and was significantly correlated with reductions in mitral regurgitant fraction (r = 0.77, p < 0.001).RESULTSMitral regurgitation by the volumetric method consistently decreased after CRT: regurgitant volume from 40 +/- 20 ml to 24 +/- 17 ml and regurgitant fraction from 40 +/- 12% to 25 +/- 14% (both: p < 0.001 vs. baseline). Normal controls had uniform segmental time-to-peak strain, with a difference of only 12 +/- 8 ms between all segments. In contrast, CRT patients at baseline had a 106 +/- 74 ms time delay between papillary muscle insertion sites (p < 0.001 vs. normal). This interpapillary muscle time delay shortened after CRT to 39 +/- 43 ms (p < 0.001 vs. baseline) and was significantly correlated with reductions in mitral regurgitant fraction (r = 0.77, p < 0.001).Cardiac resynchronization therapy significantly and immediately reduced MR. Improved coordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechanistic contributor to immediate MR reduction by CRT.CONCLUSIONSCardiac resynchronization therapy significantly and immediately reduced MR. Improved coordinated timing of mechanical activation of papillary muscle insertion sites appears to be a mechanistic contributor to immediate MR reduction by CRT.
Author SADE, L. Elif
GORCSAN, John III
SCHWARTZMAN, David
BAZAZ, Raveen
KANZAKI, Hideaki
DOHI, Kaoru
Author_xml – sequence: 1
  givenname: Hideaki
  surname: KANZAKI
  fullname: KANZAKI, Hideaki
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
– sequence: 2
  givenname: Raveen
  surname: BAZAZ
  fullname: BAZAZ, Raveen
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
– sequence: 3
  givenname: David
  surname: SCHWARTZMAN
  fullname: SCHWARTZMAN, David
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
– sequence: 4
  givenname: Kaoru
  surname: DOHI
  fullname: DOHI, Kaoru
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
– sequence: 5
  givenname: L. Elif
  surname: SADE
  fullname: SADE, L. Elif
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
– sequence: 6
  givenname: John III
  surname: GORCSAN
  fullname: GORCSAN, John III
  organization: University of Pittsburgh, Pittsburgh, Pennsylvania, United States
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16206810$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/15489094$$D View this record in MEDLINE/PubMed
BookMark eNpdkU1r3DAQhkVISDZp_0APRVDam93Rh2W7t7A0TSDQS-5mVpbWWtayK8mFzR_p362S3VDoaeCdZ-adj2ty7idvCPnAoGTA1NdduUOtSw4gS6hLEOqMrFhVNYWo2vqcrKAWVcGgra_IdYw7AFANay_JFatk00IrV-TPLR2NHtC7OFI7BerG0fQOk6HB9ItObvLUeTq6FHCfte0Sti7hq442mUDXGHKBzrl48HoIk3fPx3waTMD58I0--Oi2Q4rUhml8M9S5H2aD30c4ZoMXI5xn57fvyIXFfTTvT_GGPN19f1rfF48_fzysbx-LQQCkwiA3Ahqudduj1LCpreEbXjW6z6qVvO3txgLTSiKDWoLkLOu8l6qv0Ygb8uXYdg7Tr8XE1I0uarPfozfTEjul2gaEYBn89B-4m5bg82gdq0CxijOmMvXxRC2bfMZuDm7EcOje7p2BzycAY97fBvTaxX-c4i8vAvEXLHiVmQ
CODEN JACCDI
ContentType Journal Article
Copyright 2005 INIST-CNRS
Copyright Elsevier Limited Oct 19, 2004
Copyright_xml – notice: 2005 INIST-CNRS
– notice: Copyright Elsevier Limited Oct 19, 2004
DBID IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7T5
7TK
H94
K9.
NAPCQ
7X8
DOI 10.1016/j.jacc.2004.07.036
DatabaseName Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Immunology Abstracts
Neurosciences Abstracts
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
Immunology Abstracts
Neurosciences Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE
AIDS and Cancer Research Abstracts
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1558-3597
EndPage 1625
ExternalDocumentID 3242521291
15489094
16206810
Genre Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S
Journal Article
GrantInformation_xml – fundername: NHLBI NIH HHS
  grantid: K24 HL 04503-01
GroupedDBID ---
--K
--M
.1-
.55
.FO
.GJ
.~1
0R~
18M
1B1
1CY
1P~
1~.
1~5
29L
2WC
3O-
4.4
457
4G.
53G
5GY
5RE
5VS
6PF
7-5
71M
8P~
AABNK
AABVL
AAEDT
AAEDW
AAIKJ
AAKUH
AALRI
AAOAW
AAQFI
AAQQT
AAQXK
AAXUO
AAYWO
ABBQC
ABFNM
ABFRF
ABLJU
ABMAC
ABMZM
ABOCM
ABWVN
ABXDB
ACGFO
ACGFS
ACIUM
ACJTP
ACPRK
ACRPL
ACVFH
ADBBV
ADCNI
ADEZE
ADMUD
ADNMO
ADVLN
AEFWE
AEKER
AENEX
AEUPX
AEVXI
AEXQZ
AFCTW
AFETI
AFFNX
AFPUW
AFRAH
AFRHN
AFTJW
AGCQF
AGHFR
AGQPQ
AGYEJ
AHMBA
AIGII
AITUG
AJRQY
AKBMS
AKRWK
AKYEP
ALMA_UNASSIGNED_HOLDINGS
AMRAJ
ASPBG
AVWKF
AZFZN
BAWUL
BLXMC
CS3
DIK
DU5
E3Z
EBS
EFKBS
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FNPLU
G-Q
GBLVA
GX1
H13
HVGLF
HX~
HZ~
IHE
IQODW
IXB
J1W
J5H
K-O
KQ8
L7B
MO0
N4W
N9A
O-L
O9-
OA.
OAUVE
OK1
OL~
OZT
P-8
P-9
P2P
PC.
PQQKQ
PROAC
Q38
QTD
R2-
RIG
ROL
RPZ
SCC
SDF
SDG
SDP
SES
SEW
SSZ
TR2
UNMZH
UV1
W8F
WH7
WOQ
WOW
X7M
XPP
YYM
YYP
YZZ
Z5R
ZGI
ZXP
0SF
3V.
6I.
7RV
AACTN
AAFTH
AAYOK
ABVKL
AJOXV
AMFUW
BENPR
BPHCQ
CGR
CUY
CVF
ECM
EIF
NCXOZ
NPM
T5K
7T5
7TK
H94
K9.
NAPCQ
7X8
EFLBG
ID FETCH-LOGICAL-h300t-ea2e3082cc9da4c0b7fe2b258cd082f429dfbf01c64a1074042182f2d46d7ae3
ISSN 0735-1097
IngestDate Thu Sep 04 17:18:52 EDT 2025
Sat Jul 26 03:21:34 EDT 2025
Wed Feb 19 01:48:31 EST 2025
Mon Jul 21 09:14:03 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 8
Keywords Heart
Human
Cardiac resynchronization
Cartography
Mitral valve
Treatment
Cardiac valvular disease
Mitral regurgitation
Instrumentation therapy
Cardiovascular disease
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-h300t-ea2e3082cc9da4c0b7fe2b258cd082f429dfbf01c64a1074042182f2d46d7ae3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
PMID 15489094
PQID 1506152116
PQPubID 2031078
PageCount 7
ParticipantIDs proquest_miscellaneous_66980331
proquest_journals_1506152116
pubmed_primary_15489094
pascalfrancis_primary_16206810
PublicationCentury 2000
PublicationDate 2004-10-19
PublicationDateYYYYMMDD 2004-10-19
PublicationDate_xml – month: 10
  year: 2004
  text: 2004-10-19
  day: 19
PublicationDecade 2000
PublicationPlace New York, NY
PublicationPlace_xml – name: New York, NY
– name: United States
– name: New York
PublicationTitle Journal of the American College of Cardiology
PublicationTitleAlternate J Am Coll Cardiol
PublicationYear 2004
Publisher Elsevier Science
Elsevier Limited
Publisher_xml – name: Elsevier Science
– name: Elsevier Limited
SSID ssj0006819
Score 2.3352106
Snippet We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from improved...
Objectives We tested the hypothesis that an immediate reduction in mitral regurgitation (MR) after cardiac resynchronization therapy (CRT) results from...
SourceID proquest
pubmed
pascalfrancis
SourceType Aggregation Database
Index Database
StartPage 1619
SubjectTerms Aged
Biological and medical sciences
Biomechanical Phenomena - instrumentation
Blood pressure
Bundle-Branch Block - diagnostic imaging
Bundle-Branch Block - physiopathology
Bundle-Branch Block - therapy
Cardiology
Cardiology. Vascular system
Cardiovascular disease
Classical genetics, quantitative genetics, hybrids
Echocardiography, Doppler
Echocardiography, Doppler, Color - instrumentation
Electrodes, Implanted
Endocardial and cardiac valvular diseases
Female
Fundamental and applied biological sciences. Psychology
Genetics of eukaryotes. Biological and molecular evolution
Heart
Heart failure
Human
Humans
Image Processing, Computer-Assisted - instrumentation
Male
Medical sciences
Microcomputers
Middle Aged
Mitral Valve Insufficiency - diagnostic imaging
Mitral Valve Insufficiency - physiopathology
Mitral Valve Insufficiency - therapy
Mortality
Myocardial Contraction - physiology
Pacemaker, Artificial
Papillary Muscles - physiopathology
Software
Stroke
Stroke Volume - physiology
Studies
Treatment Outcome
Ventricular Function, Left - physiology
Title A mechanism for immediate reduction in mitral regurgitation after Cardiac resynchronization therapy: Insights from mechanical activation strain mapping
URI https://www.ncbi.nlm.nih.gov/pubmed/15489094
https://www.proquest.com/docview/1506152116
https://www.proquest.com/docview/66980331
Volume 44
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fb9MwELaqISFeEL8pjOEH3qZUaeI4yWM1bZpgGxJkUt8ix3bWTmqK2gREH_ij-Au5s02S0oKAlyhyJFfxfTmfr999R8ibFCXOeVx44Ae4x5SQXiIi6cFeKFALBKIKrHe-vOLn1-ztNJoOBt97rKWmLkZys7eu5H-sCmNgV6yS_QfLtpPCANyDfeEKFobrX9l4crzQWLmLjS6QLjhfmEKQGluhKCsLi_mMxRzTGTB206xunCa3aw4uDUBQxXn9tZJGKNfWZR7XPbmB3eC1V5BS9ZMPJ4be2s_Uv4PgU7je2HOl4bZLnm6ESV9_EJ91V5H2Uc6-wLtuXGq2R7rHfsozyz4Qy1WzlbBg6Ol7brGtpNmt4IpDVEW1fN2Rdg45SrwwcmPOY1vFSIfMpOd-IXxN9-4LNkVxO7oV0uhWMqPYGu4R4b56n59dX1zk2ek0235qN308osF2j4IJd4IY4jXwoaNvHa2IJ6aZTPsurlDLcgp__Xlk4oo1fIyl7aLy-2OOCXeyB-S-MzWdWNA9JANdPSJ3Lx0T4zGRE9pijwL2aIs92mKPzitqsUe3sEcN9qjDHt3BHnXYe0Kys9Ps5NxzDTu8Wej7tadFoFH-SMpUCSb9Ii51UARRIhWMlhD6qLIo_bHkTCARGDYMON6WgWJcxUKHT8lBtaz0c0JLFWsWiiAVKmWalWkBcXTpcw2-RcYyHpKjrYXLP1ltlnzMAzSBPySHP1cyd1_sOkc1TYxXx3xIXrePwZ_in2Si0stmnXOeJn4YjofkmV3_bmo43Kd-yl78eeqX5F6H-kNyUK8a_QoC17o4Mkj5AaIvnzo
linkProvider Elsevier
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=A+mechanism+for+immediate+reduction+in+mitral+regurgitation+after+cardiac+resynchronization+therapy&rft.jtitle=Journal+of+the+American+College+of+Cardiology&rft.au=Kanzaki%2C+Hideaki&rft.au=Bazaz%2C+Raveen&rft.au=Schwartzman%2C+David&rft.au=Dohi%2C+Kaoru&rft.date=2004-10-19&rft.pub=Elsevier+Limited&rft.issn=0735-1097&rft.eissn=1558-3597&rft.volume=44&rft.issue=8&rft.spage=1619&rft_id=info:doi/10.1016%2Fj.jacc.2004.07.036&rft.externalDBID=NO_FULL_TEXT&rft.externalDocID=3242521291
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0735-1097&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0735-1097&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0735-1097&client=summon