Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI

User menu

  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Nuclear Medicine
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI
  • Subscribe
  • My alerts
  • Log in
  • My Cart
Journal of Nuclear Medicine

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • View or Listen to JNM Podcast
  • Visit JNM on Facebook
  • Join JNM on LinkedIn
  • Follow JNM on Twitter
  • Subscribe to our RSS feeds
Research ArticleClinical Investigation

Impaired Cardiac Sympathetic Innervation and Myocardial Perfusion Are Related to Lethal Arrhythmia: Quantification of Cardiac Tracers in Patients with ICDs

Kimio Nishisato, Akiyoshi Hashimoto, Tomoaki Nakata, Takahiro Doi, Hitomi Yamamoto, Daigo Nagahara, Shinya Shimoshige, Satoshi Yuda, Kazufumi Tsuchihashi and Kazuaki Shimamoto
Journal of Nuclear Medicine August 2010, 51 (8) 1241-1249; DOI: https://doi.org/10.2967/jnumed.110.074971
Kimio Nishisato
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Akiyoshi Hashimoto
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Tomoaki Nakata
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Takahiro Doi
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Hitomi Yamamoto
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Daigo Nagahara
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Shinya Shimoshige
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Satoshi Yuda
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kazufumi Tsuchihashi
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kazuaki Shimamoto
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • FIGURE 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 1.

    Receiver-operating-characteristic analysis using cardiac metaiodobenzylguanidine activity (late HMR) and tetrofosmin SS for identification of patients with primary cardiac event. Metaiodobenzylguanidine HMR of 1.90 and tetrofosmin SS of 12 were selected as optimal cutoff values. TF = tetrofosmin.

  • FIGURE 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 2.

    Scatterplots of patients with (●) and without (○) primary cardiac events who were divided into 3 groups based on cutoff vales of cardiac metaiodobenzylguanidine activity and tetrofosmin uptake identified by receiver-operating-characteristic analysis. There are significant (P < 0.05) differences in event rate among the 3 groups (94% for group with impaired metaiodobenzylguanidine and tetrofosmin uptake, 45% for group with impaired metaiodobenzylguanidine and preserved tetrofosmin uptake, and 18% for group with preserved metaiodobenzylguanidine and tetrofosmin uptake). Unshaded area = preserved uptake of both metaiodobenzylguanidine and tetrofosmin (n = 22); dotted area = impaired metaiodobenzylguanidine uptake and preserved tetrofosmin uptake (n = 20); shaded area = impaired uptake of both metaiodobenzylguanidine and tetrofosmin (n = 18). MIBG = metaiodobenzylguanidine; TF = tetrofosmin.

  • FIGURE 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 3.

    Kaplan–Meier event-free curves of 3 groups based on metaiodobenzylguanidine and tetrofosmin uptake show that patients with impaired uptake of both metaiodobenzylguanidine and tetrofosmin had significantly lower event-free rate than did patients in the other 2 groups. MIBG = metaiodobenzylguanidine; TF = tetrofosmin.

  • FIGURE 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 4.

    Scatterplots of patients with (●) and without (○) primary cardiac events when 31 patients with LVEF of 50% or more are considered. Patient group with impaired uptake of both metaiodobenzylguanidine and tetrofosmin had greatest (P < 0.05) event rate (100%) when compared with other groups (16%–30%). Unshaded area = preserved uptake of both metaiodobenzylguanidine and tetrofosmin (n = 19); dotted area = impaired metaiodobenzylguanidine uptake and preserved tetrofosmin uptake (n = 9); shaded area = impaired uptake of both metaiodobenzylguanidine and tetrofosmin (n = 3). MIBG = metaiodobenzylguanidine; TF = tetrofosmin.

  • FIGURE 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 5.

    Kaplan–Meier event-free curves of 3 groups based on metaiodobenzylguanidine and tetrofosmin uptake when 31 patients with LVEF of 50% or more are considered. Patients with impaired uptake of both metaiodobenzylguanidine and tetrofosmin had significantly lower event-free rate than did group with preserved uptake of both metaiodobenzylguanidine and tetrofosmin. MIBG = metaiodobenzylguanidine; TF = tetrofosmin.

  • FIGURE 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 6.

    Planar metaiodobenzylguanidine images and planar and tomographic tetrofosmin images. (A) A 56-y-old woman had both markedly reduced metaiodobenzylguanidine activity (HMR of 1.21) and perfusion uptake (tetrofosmin SPECT SS of 16) and underwent ICD shocks 3 mo after implantation because of electrical storm of ventricular tachyarrhythmia. (B) A 60-y-old man had highly dilated left ventricle but nearly normal cardiac metaiodobenzylguanidine activity (HMR of 2.02) and perfusion score (tetrofosmin SS of 4). Neither ICD shock nor other lethal cardiac event was observed during follow-up. MIBG = metaiodobenzylguanidine; TF = tetrofosmin.

Tables

  • Figures
    • View popup
    TABLE 1.

    Comparison of Clinical Backgrounds Between Patients With and Without Primary Endpoints

    ParameterPatients with cardiac events (n = 30)Patients without cardiac events (n = 30)P
    Mean age ± SD (y)53.3 ± 15.053.4 ± 12.1NS
    Sex (female)8 (27)11 (37)NS
    Coronary risk factors
     Diabetes mellitus8 (27)4 (13)NS
     Hypertension7 (23)8 (27)NS
     Dyslipidemia14 (47)7 (23)NS
     Chronic renal failure2 (7)3 (10)NS
    Underlying cardiac disease
     Prior myocardial infarction8 (27)3 (10)
     Dilated cardiomyopathy15 (50)7 (23)
     Hypertrophic cardiomyopathy2 (7)5 (17)NS
     Arrhythmogenic right ventricular dysplasia2 (7)4 (13)
     Brugada syndrome1 (3)9 (30)
     Idiopathic ventricular arrhythmia2 (7)2 (7)
    NYHA functional classNS
     I1525
     II03
     III140
     IV12
    Mean follow-up period ± SD (mo)31 ± 1728 ± 15NS
    ECG (mean ± SD)
     LVEF (%)42 ± 1856 ± 150.002
     Left ventricular end-diastolic diameter (mm)57 ± 1150 ± 110.017
     BNP (pg/mL)209 ± 198101 ± 1400.018
    Presenting arrhythmia before ICD implantation
     VF6 (20)7 (23)NS
     Sustained VT18 (60)8 (27)0.02
     Nonsustained VT6 (20)5 (17)NS
    Electrophysiologic study
     Inducible VT17 (57)12 (40)NS
     Inducible VF16 (53)10 (33)NS
    Concomitant medication
     Diuretic14 (47)6 (20)NS
     Spironolactone15 (50)4 (13)0.005
     Digitalis3 (10)0 (0)NS
     β-blocker22 (73)11 (37)0.011
     ACEI/ARB19 (63)9 (30)0.02
     Nitrate6 (20)1 (3)NS
    • NS= not significant; NYHA = New York Heart Association; VF = ventricular fibrillation; VT = ventricular tachyarrhythmias; ACEI = angiotensin converting enzyme inhibitor; ARB = angiotensin II receptor blocker.

    • Data in parentheses are percentages.

    • View popup
    TABLE 2.

    Comparison of Scintigraphic Data Between Patients With and Without Primary Endpoints

    ParameterPatients with cardiac events (n = 30)Patients without cardiac events (n = 30)P
    Metaiodobenzylguanidine
     Early HMR1.96 ± 0.262.16 ± 0.370.019
     Late HMR1.73 ± 0.342.06 ± 0.460.003
     Washout rate33.1 ± 14.028.6 ± 11.0NS
    Tetrofosmin
     SS18.0 ± 16.25.7 ± 4.40.000
     LVEF36 ± 1954 ± 130.000
     LVEDV187 ± 117109 ± 870.005
     LVESV157 ± 12175 ± 740.002
    • NS = not significant; LVEDV = left ventricular end-diastolic volume; LVESV = left ventricular end-systolic volume.

    • Values are shown as mean ± SD.

    • View popup
    TABLE 3.

    Univariate and Multivariate Logic Regression Analyses

    UnivariateMultivariate (Cox proportional hazards model)
    95% Confidence interval95% Confidence interval
    ParameterWaldHazard ratioLowerUpperPWaldHazard ratioLowerUpperP
    Age (y)0.0500.9970.9691.0260.824
    Sex0.9081.4890.6573.3760.341
    Clinical VT/VF3.9924.341.02818.3130.046
    Inducible VT/VF0.2100.8390.3961.7790.647
    SAECG0.5741.4920.5304.1980.449
    Medications1.6151.6290.7673.4590.204
    BNP4.5791.0021.0001.0040.0320.6551.0010.9981.0040.418
    HMR (late)7.7710.2050.0670.6250.005
    Washout0.6631.0140.9811.0470.415
    HMR ≦ 1.98.5095.9661.79719.8060.0043.7054.5600.97321.3740.054
    Tetrofosmin SS13.5471.0431.0201.0670.000
    Tetrofosmin SS ≧ 1213.6914.0221.9248.4080.0004.0832.8421.0327.8300.043
    HMR ≦ 1.9 and tetrofosmin SS ≧ 1213.6914.0221.9248.4080.0006.4543.8571.36110.9280.011
    LVEF4.1880.9780.9580.9990.0410.8900.3460.9831.0510.346
    • VT = ventricular tachycardia; VF = ventricular fibrillation; SAECG = signal-averaged electrocardiographic findings.

PreviousNext
Back to top

In this issue

Journal of Nuclear Medicine: 51 (8)
Journal of Nuclear Medicine
Vol. 51, Issue 8
August 1, 2010
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Journal of Nuclear Medicine.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Impaired Cardiac Sympathetic Innervation and Myocardial Perfusion Are Related to Lethal Arrhythmia: Quantification of Cardiac Tracers in Patients with ICDs
(Your Name) has sent you a message from Journal of Nuclear Medicine
(Your Name) thought you would like to see the Journal of Nuclear Medicine web site.
Citation Tools
Impaired Cardiac Sympathetic Innervation and Myocardial Perfusion Are Related to Lethal Arrhythmia: Quantification of Cardiac Tracers in Patients with ICDs
Kimio Nishisato, Akiyoshi Hashimoto, Tomoaki Nakata, Takahiro Doi, Hitomi Yamamoto, Daigo Nagahara, Shinya Shimoshige, Satoshi Yuda, Kazufumi Tsuchihashi, Kazuaki Shimamoto
Journal of Nuclear Medicine Aug 2010, 51 (8) 1241-1249; DOI: 10.2967/jnumed.110.074971

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Impaired Cardiac Sympathetic Innervation and Myocardial Perfusion Are Related to Lethal Arrhythmia: Quantification of Cardiac Tracers in Patients with ICDs
Kimio Nishisato, Akiyoshi Hashimoto, Tomoaki Nakata, Takahiro Doi, Hitomi Yamamoto, Daigo Nagahara, Shinya Shimoshige, Satoshi Yuda, Kazufumi Tsuchihashi, Kazuaki Shimamoto
Journal of Nuclear Medicine Aug 2010, 51 (8) 1241-1249; DOI: 10.2967/jnumed.110.074971
Twitter logo Facebook logo LinkedIn logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSION
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

Related Articles

  • 123I-Metaiodobenzylguanidine Imaging in the Era of Implantable Cardioverter Defibrillators: Beyond Ejection Fraction
  • PubMed
  • Google Scholar

Cited By...

  • Sympathetic structural and electrophysiological remodeling in a rabbit model of reperfused myocardial infarction
  • Chondroitin Sulfate Proteoglycan 4,6 sulfation regulates sympathetic nerve regeneration after myocardial infarction
  • Nuclear Imaging of the Cardiac Sympathetic Nervous System: A Disease-Specific Interpretation in Heart Failure
  • Molecular Mechanisms of Sympathetic Remodeling and Arrhythmias
  • The Nervous Heart: Role of Sympathetic Reinnervation in Cardiac Regeneration
  • Predicting Risk Versus Predicting Potential Survival Benefit Using 123I-mIBG Imaging in Patients With Systolic Dysfunction Eligible for Implantable Cardiac Defibrillator Implantation: Analysis of Data From the Prospective ADMIRE-HF Study
  • Introduction to Cardiac Neuronal Imaging: A Clinical Perspective
  • Cardiac 123I-MIBG Imaging for Clinical Decision Making: 22-Year Experience in Japan
  • A Pooled Analysis of Multicenter Cohort Studies of 123I-mIBG Imaging of Sympathetic Innervation for Assessment of Long-Term Prognosis in Heart Failure
  • Infarct-Derived Chondroitin Sulfate Proteoglycans Prevent Sympathetic Reinnervation after Cardiac Ischemia-Reperfusion Injury
  • Cardiac iodine-123 metaiodobenzylguanidine imaging predicts ventricular arrhythmia in heart failure patients receiving an implantable cardioverter-defibrillator for primary prevention
  • Cardiac Mortality Assessment Improved by Evaluation of Cardiac Sympathetic Nerve Activity in Combination with Hemoglobin and Kidney Function in Chronic Heart Failure Patients
  • 123I-Metaiodobenzylguanidine Imaging in the Era of Implantable Cardioverter Defibrillators: Beyond Ejection Fraction
  • Google Scholar

More in this TOC Section

  • First-in-Human Study of 18F-Labeled PET Tracer for Glutamate AMPA Receptor [18F]K-40: A Derivative of [11C]K-2
  • Detection of HER2-Low Lesions Using HER2-Targeted PET Imaging in Patients with Metastatic Breast Cancer: A Paired HER2 PET and Tumor Biopsy Analysis
  • [11C]Carfentanil PET Whole-Body Imaging of μ-Opioid Receptors: A First in-Human Study
Show more Clinical Investigation

Similar Articles

SNMMI

© 2025 SNMMI

Powered by HighWire