4.7 Article

Morphological, Functional, and Tissue Characterization of Silent Myocardial Involvement in Patients With Primary Biliary Cholangitis

Journal

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY
Volume 20, Issue 5, Pages 1112-+

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cgh.2021.08.035

Keywords

Primary Biliary Cholangitis; Myocardial Impairment; Extracellular Matrix; Cardiac Magnetic Resonance

Funding

  1. National Science Fund for Distinguished Young Scholars [81625002]
  2. National Natural Science Foundation of China [81620108002, 81771732, 81830016, 81570469, 81421001, 81971570]
  3. Shanghai Outstanding Academic Leaders Program [18XD1402400]
  4. Shanghai Science and Technology Commission [20Y11910500, 21XD1432100]
  5. Clinical Research Plan of SHDC [SHDC2020CR2025B]
  6. Shanghai Municipal Education Commission Gaofeng Clinical Medicine Grant Support [20172014]
  7. Shanghai Pudong Health Development Center [PW2018D-03]
  8. Shanghai Jiaotong University [YG2019ZDA13]
  9. University of Shanghai for Science and Technology [10-20-302-425]

Ask authors/readers for more resources

This study identifies clinically silent cardiac impairment in PBC patients without cardiac manifestations, using cardiac imaging techniques. Specific CMR patterns of myocardial involvement were detected, allowing for optimal screening and potentially timely therapies for early myocardial impairment.
BACKGROUND & AIMS: Cirrhotic cardiomyopathy is a major complication and cause of morbidity in end-stage primary biliary cholangitis (PBC). However, it is unclear whether there is clinically silent myocardial involvement at the early stage of PBC before cirrhosis and cardiac manifestations. This prospective, three-center, multi-modality cardiac imaging study on the early identification of myocardial impairment in PBC (EARLY-MYO-PBC) was designed to identify silent myocardial impairment in PBC patients without cardiac manifestations. METHODS: A total of 112 subjects (56 with PBC and 56 age- and sex-matched controls) undergoing cardiovascular magnetic resonance (CMR) were enrolled. Demographic, serologic, and cardiac imaging data were prospectively collected. All participants had no cardiac discomfort or previous heart disease and had normal electrocardiographic findings. RESULTS: Subclinical myocardial involvement, as evidenced by cardiac morphologic, functional, and tissue characterization changes on CMR, including hyperdynamic left ventricular (LV) ejection fraction (median, 75% in PBC patients vs 69% in controls, P = .029), subclinical myocardial edema by T2-short tau inversion recovery (21% vs 2% in controls, P = .001), elevated extracellular matrix indices (30% vs 26% in controls, P < .001), and impaired myocardial viability by positive late gadolinium enhancement (LGE) (36%), was detected in PBC patients. Importantly, a mid-wall stripe at the LV septum was identified as a PBC-specific LGE pattern that differs from other known cardiomyopathies. In multivariate analysis, gp210 positivity (odds ratio [OR] = 9.909, P = .010), lower hemoglobin (OR = 0.919, P = .004), and body mass index (OR = 0.638, P = .005) were independent predictors of cardiac abnormalities in PBC. CONCLUSIONS: This study demonstrates clinically silent cardiac impairment with specific CMR patterns in PBC, allowing optimal screening for early myocardial impairment and potentially timely therapies. (Trial registration no.: NCT03545672)

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