Gabriela Nunes Leal, Camila Astley, Marcos Santos Lima, Maria de Fátima Rodrigues Diniz, Alessandro Cavalcanti Lianza, Karen Saori Shiraishi Sawamura, Carolina Rocha Brito Menezes, Camila Lino Martins Rodrigues da Silva, Vera Bain, Rodrigo Imada, William Chalela, Maria Fernanda Badue Pereira, Heloisa Helena de Sousa Marques, Carlos Alberto Buchpiguel, Bruno Gualano, Clovis Artur Silva
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Autopsy studies suggested that microvascular dysfunction may be relevant to LV impairment.</p>\n </section>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>We aimed to evaluate segmental LV longitudinal strain by 2DST echocardiography and myocardial flow reserve (MFR) by 13 N-ammonia PET-CT, in <b>six</b> surviving MIS-c patients.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Each patient generated 34 LV segments for combined 2DST and MRF analysis. MFR was considered abnormal when <2, borderline when between 2 and 2.5 and normal when >2.5.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>From July 2020 to February 2021, six patients were admitted with MIS-c: three males, aged 9.3 (6.6–15.7) years. Time from admission to the follow-up visit was 6.05 (2–10.3) months. Although all patients were asymptomatic and LV EF was ≥55%, 43/102 (42.1%) LV segments showed MFR <2.5. There was a modest positive correlation between segmental peak systolic longitudinal strain and MFR: <i>r</i> = .36, <i>p</i> = .03 for basal segments; <i>r</i> = .41, <i>p</i> = .022 for mid segments; <i>r</i> = .42, <i>p</i> = .021 for apical segments. Median peak systolic longitudinal strain was different among MRF categories: 18% (12%–24%) for abnormal, 18.5% (11%–35%) for borderline, and 21% (12%–32%) for normal MFR (<i>p</i> = .006).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>We provided preliminary evidence that surviving MIS-c patients may present subclinical impairment of myocardial microcirculation. 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Pathophysiological mechanisms involved in myocardial injury were scarcely investigated, and cardiovascular outcomes are uncertain. Autopsy studies suggested that microvascular dysfunction may be relevant to LV impairment.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>We aimed to evaluate segmental LV longitudinal strain by 2DST echocardiography and myocardial flow reserve (MFR) by 13 N-ammonia PET-CT, in <b>six</b> surviving MIS-c patients.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Each patient generated 34 LV segments for combined 2DST and MRF analysis. MFR was considered abnormal when <2, borderline when between 2 and 2.5 and normal when >2.5.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>From July 2020 to February 2021, six patients were admitted with MIS-c: three males, aged 9.3 (6.6–15.7) years. Time from admission to the follow-up visit was 6.05 (2–10.3) months. 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引用次数: 4
摘要
儿童多系统炎症综合征(MIS-c)与严重心血管损害和最终死亡相关。涉及心肌损伤的病理生理机制很少被研究,心血管结果也不确定。尸检研究表明微血管功能障碍可能与左室损伤有关。目的通过2DST超声心动图和13例n -氨PET-CT评价6例存活的MIS-c患者的左室节段纵向应变和心肌血流储备(MFR)。方法每个患者生成34个LV段,进行2DST和MRF联合分析。MFR在<2时为异常,在2 - 2.5之间为边缘,在>2.5时为正常。结果2020年7月至2021年2月,6例MIS-c患者入院:男性3例,年龄9.3(6.6-15.7)岁。入院至随访时间为6.05(2-10.3)个月。虽然所有患者均无症状且左室EF≥55%,但43/102(42.1%)左室节段显示MFR <2.5。节段收缩纵向应变峰值与MFR呈中度正相关:r = 0.36,基底节段p = 0.03;R = 0.41, p = 0.022;根尖段R = 0.42, p = 0.021。收缩纵向应变中位数峰值在不同MRF类别中存在差异:异常MFR为18%(12% ~ 24%),交界MFR为18.5%(11% ~ 35%),正常MFR为21% (12% ~ 32%)(p = 0.006)。结论我们提供了初步证据,存活的misc患者可能存在亚临床心肌微循环损害。鉴于其与13 n -氨PET-CT衍生MFR的良好相关性,节段性心脏应变评估似乎对MIS-c心血管随访有用。
Segmental cardiac strain assessment by two-dimensional speckle-tracking echocardiography in surviving MIS-c patients: Correlations with myocardial flow reserve (MFR) by 13 N-ammonia PET-CT
Background
Multisystem inflammatory syndrome in children (MIS-c) is associated with severe cardiovascular impairment and eventually death. Pathophysiological mechanisms involved in myocardial injury were scarcely investigated, and cardiovascular outcomes are uncertain. Autopsy studies suggested that microvascular dysfunction may be relevant to LV impairment.
Objective
We aimed to evaluate segmental LV longitudinal strain by 2DST echocardiography and myocardial flow reserve (MFR) by 13 N-ammonia PET-CT, in six surviving MIS-c patients.
Methods
Each patient generated 34 LV segments for combined 2DST and MRF analysis. MFR was considered abnormal when <2, borderline when between 2 and 2.5 and normal when >2.5.
Results
From July 2020 to February 2021, six patients were admitted with MIS-c: three males, aged 9.3 (6.6–15.7) years. Time from admission to the follow-up visit was 6.05 (2–10.3) months. Although all patients were asymptomatic and LV EF was ≥55%, 43/102 (42.1%) LV segments showed MFR <2.5. There was a modest positive correlation between segmental peak systolic longitudinal strain and MFR: r = .36, p = .03 for basal segments; r = .41, p = .022 for mid segments; r = .42, p = .021 for apical segments. Median peak systolic longitudinal strain was different among MRF categories: 18% (12%–24%) for abnormal, 18.5% (11%–35%) for borderline, and 21% (12%–32%) for normal MFR (p = .006).
Conclusion
We provided preliminary evidence that surviving MIS-c patients may present subclinical impairment of myocardial microcirculation. Segmental cardiac strain assessment 2DST seems useful for MIS-c cardiovascular follow-up, given its good correlation with 13 N-ammonia PET-CT derived MFR.
期刊介绍:
The journal features original contributions that are the result of investigations contributing significant new information relating to the vascular and lymphatic microcirculation addressed at the intact animal, organ, cellular, or molecular level. Papers describe applications of the methods of physiology, biophysics, bioengineering, genetics, cell biology, biochemistry, and molecular biology to problems in microcirculation.
Microcirculation also publishes state-of-the-art reviews that address frontier areas or new advances in technology in the fields of microcirculatory disease and function. Specific areas of interest include: Angiogenesis, growth and remodeling; Transport and exchange of gasses and solutes; Rheology and biorheology; Endothelial cell biology and metabolism; Interactions between endothelium, smooth muscle, parenchymal cells, leukocytes and platelets; Regulation of vasomotor tone; and Microvascular structures, imaging and morphometry. Papers also describe innovations in experimental techniques and instrumentation for studying all aspects of microcirculatory structure and function.