Rheumatology (Oxford, England) · 2026
Coronary microvascular dysfunction in systemic sclerosis: insights from PET-derived myocardial flow reserve.
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Williams Kenneth, Emokpae Morgan, Koyi Bindu, Csecs Ibolya, Gunes Ilayda, Frohlich Bailey, Sinusas Albert J, Hinchcliff Monique, Feher Attila
Аннотация
OBJECTIVES: Cardiovascular death is the second leading cause in systemic sclerosis (SSc), with coronary microvascular dysfunction (CMVD) playing a key role. PET-derived myocardial blood flow (MBF) and flow reserve (MFR) offer a validated, non-invasive way to assess CMVD. We studied the prevalence of impaired MFR in SSc and its association with vasodilator or immunomodulatory therapy.
METHODS: SSc patients who underwent dynamic 82-Rubidium PET myocardial perfusion imaging (MPI) at Yale New Haven Hospital (July 2016 to April 2025) were studied. Patients were matched 3:1 with controls without autoimmune rheumatologic disease based on age, sex, BMI and cardiovascular comorbidities. Abnormal MFR was defined as <2.0.
RESULTS: The cohort included 67 SSc patients (87% female, age: 61 ± 11 years, 21% diffuse cutaneous SSc, SSc duration: 12 ± 10 years) and 201 controls. Rest MBF was higher in SSc (1.14 [IQR 0.91-1.39] ml/g/min) vs controls (1.00 [IQR 0.78-1.25]; P = 0.01), while MFR was lower (2.17 [IQR 1.84-2.57] vs 2.44 [IQR 1.96-2.96]; P = 0.01). Stress MBF was similar (2.47 [IQR 1.99-2.82] vs 2.43 [IQR 1.91-3.04]; P = 0.85). Multivariable analysis showed MMF use linked to lower odds of abnormal MFR (OR 0.09 [95% CI 0.01-0.56]; P = 0.017), while calcium channel blockers (OR 7.77 [1.93-42.53]; P = 0.008) and statins (OR 7.14 [1.86-36.87]; P = 0.008) increased odds.
CONCLUSIONS: PET MPI reveals reduced MFR in SSc. Treatment associations, including MMF, should be interpreted cautiously given the retrospective design. PET-derived MFR may serve as a non-invasive marker of vascular involvement, warranting prospective validation.
METHODS: SSc patients who underwent dynamic 82-Rubidium PET myocardial perfusion imaging (MPI) at Yale New Haven Hospital (July 2016 to April 2025) were studied. Patients were matched 3:1 with controls without autoimmune rheumatologic disease based on age, sex, BMI and cardiovascular comorbidities. Abnormal MFR was defined as <2.0.
RESULTS: The cohort included 67 SSc patients (87% female, age: 61 ± 11 years, 21% diffuse cutaneous SSc, SSc duration: 12 ± 10 years) and 201 controls. Rest MBF was higher in SSc (1.14 [IQR 0.91-1.39] ml/g/min) vs controls (1.00 [IQR 0.78-1.25]; P = 0.01), while MFR was lower (2.17 [IQR 1.84-2.57] vs 2.44 [IQR 1.96-2.96]; P = 0.01). Stress MBF was similar (2.47 [IQR 1.99-2.82] vs 2.43 [IQR 1.91-3.04]; P = 0.85). Multivariable analysis showed MMF use linked to lower odds of abnormal MFR (OR 0.09 [95% CI 0.01-0.56]; P = 0.017), while calcium channel blockers (OR 7.77 [1.93-42.53]; P = 0.008) and statins (OR 7.14 [1.86-36.87]; P = 0.008) increased odds.
CONCLUSIONS: PET MPI reveals reduced MFR in SSc. Treatment associations, including MMF, should be interpreted cautiously given the retrospective design. PET-derived MFR may serve as a non-invasive marker of vascular involvement, warranting prospective validation.