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Research ArticleCLINICAL INVESTIGATIONS

Mechanisms of Progression and Regression of Coronary Artery Disease by PET Related to Treatment Intensity and Clinical Events at Long-Term Follow-up

Stefano Sdringola, Catalin Loghin, Fernando Boccalandro and K. Lance Gould
Journal of Nuclear Medicine January 2006, 47 (1) 59-67;
Stefano Sdringola
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Catalin Loghin
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Fernando Boccalandro
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K. Lance Gould
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  • FIGURE 1. 
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    FIGURE 1. 

    Orientation of PET perfusion images.

  • FIGURE 2. 
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    FIGURE 2. 

    Schematic of stress PET images after dipyridamole at baseline compared with follow-up PET in various quadrant pairings. Small orange area signifies a mild small dipyridamole-induced perfusion defect. Green medium-sized area signifies a moderate medium-sized dipyridamole-induced perfusion defect. Large blue area signifies a severe large dipyridamole-induced defect. BW at follow-up may be worse (arrow A) or better (arrow B). FuW may be the same quadrant as baseline (arrow A) or a different quadrant than at baseline (arrow C). MCh may be a different quadrant than the baseline worst, either worse (arrow C) or better (arrow D).

  • FIGURE 3. 
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    FIGURE 3. 

    (A) PET perfusion images at rest (top row) and after dipyridamole (middle row) at baseline and after dipyridamole at follow-up (bottom row) illustrating progression. In color bar, white indicates the highest myocardial uptake of radionuclide reflecting the highest myocardial perfusion, with red being the next highest and progressively lower perfusion indicated by color gradations from red to yellow, green, and blue. At baseline, the lateral quadrant has the worst defect, whereas at follow-up, the inferior wall has the worst defect, illustrating that most patients had changes in quadrants other than the baseline worst quadrant. (B) PET perfusion images after dipyridamole at baseline and at follow-up illustrating regression.

  • FIGURE 4. 
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    FIGURE 4. 

    Percentage of patients in whom the quadrant pair with the maximal change from baseline to follow-up (MCh) improved (better) or became more severe (worse) for each treatment group (P < 0.001).

  • FIGURE 5. 
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    FIGURE 5. 

    Percentage of patients with the FuW in a different region than at baseline that was also more severe than at baseline for each treatment group (P = 0.01).

  • FIGURE 6. 
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    FIGURE 6. 

    Percentage of patients in whom the BW became better, worse, or showed no change in each treatment group (P = 0.02).

  • FIGURE 7. 
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    FIGURE 7. 

    Quantitative change in severity (average quadrant activity) from baseline–to–follow-up PET for the quadrant pair with maximum baseline–to–follow-up change, MCh (A), and for the quadrant with the worst defect at baseline, BW (B). Vertical axis values are mean delta or mean change in relative normalized activity expressed as % of maximum as defined in the text, not 2% change (P ≤ 0.001 for A and B).

Tables

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    TABLE 1

    Normal Values and Reproducibility

    MeasurementHealthy subjects mean value (%)1 SD* (%)Patients PET 1† (%)1 SD (%)Patients PET 2† (%)1 SD (%)Mean Δ P2 – P1 (%)Mean Δ of P1 (%)P1 vs. P2
    Lowest quadrant average % of maximal activity78±862±1363±11+0.0040.7NS
    %LV
     <2.5 SD0013.9±1412.7±17.2−1.28.6NS
     <60% maximum0016.7±14.615.4±14.8−1.37.8NS
    • ↵* n = 20.

    • ↵† n = 10.

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    TABLE 2

    Quadrant Pairings

    Quadrant pairQuadrant definedFollow-up comparison
    BWBaseline worstCompared with same quadrant at follow-up
    FuWFollow-up worstCompared with same quadrant at baseline
    MChMaximal changeBaseline follow-up pair with greatest change
    Combined Quadrant changeBW, FuW, MChAll 3 better, worse, or mixed*
    • ↵* See text.

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    TABLE 3

    Patient Characteristics

    Baseline characteristics*Value
    Age (y)59 ± 9.4
    No. (%) of patients
     Men364 (89)
     Women45 (11)
     Systemic hypertension166 (40)
     Diabetes mellitus30 (7)
     Family history of CAD281 (68)
     History of myocardial infarction123 (30)
    Total cholesterol (mg/dL)210 ± 46
    Triglycerides (mg/dL)157 ± 75
    HDLs (mg/dL)44 ± 19
    LDLs (mg/dL)137 ± 43
    Left ventricular ejection fraction (%)57 ± 12
    • ↵* n = 409.

    • View popup
    TABLE 4

    PET Perfusion Changes at Follow-up as Predictors of Long-Term Cardiovascular Events by Stepwise Multivariate Logistic Regression Analysis

    Myocardial perfusion changesOdds ratio95% CIP value
    Change in size of perfusion defect1.113.9 ± 0.70.3
    Change in severity of perfusion defect*1.31.9 ± 0.70.3
    Change in severity of baseline worst perfusion defect*0.991.2 ± 0.60.5
    Maximal change in perfusion in any quadrant*1.142.7 ± 0.70.3
    Whole heart change in combined size–severity of perfusion defects3.325.9 ± 2.10.01
    Combined Quadrants change in perfusion defects2.573.1 ± 1.60.02
    • ↵* Refers to 1 quadrant, not the whole myocardium.

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Journal of Nuclear Medicine: 47 (1)
Journal of Nuclear Medicine
Vol. 47, Issue 1
January 2006
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Mechanisms of Progression and Regression of Coronary Artery Disease by PET Related to Treatment Intensity and Clinical Events at Long-Term Follow-up
Stefano Sdringola, Catalin Loghin, Fernando Boccalandro, K. Lance Gould
Journal of Nuclear Medicine Jan 2006, 47 (1) 59-67;

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Mechanisms of Progression and Regression of Coronary Artery Disease by PET Related to Treatment Intensity and Clinical Events at Long-Term Follow-up
Stefano Sdringola, Catalin Loghin, Fernando Boccalandro, K. Lance Gould
Journal of Nuclear Medicine Jan 2006, 47 (1) 59-67;
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