Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of LMNA Mutation Carriers?
P Chmielewski, E Michalak, I Kowalik… - Journal of Clinical …, 2020 - mdpi.com
P Chmielewski, E Michalak, I Kowalik, M Franaszczyk, M Sobieszczanska-Malek…
Journal of Clinical Medicine, 2020•mdpi.comMutations in the lamin A/C gene are variably phenotypically expressed; however, it is
unclear whether circulating cardiac biomarkers are helpful in the detection and risk
assessment of cardiolaminopathies. We sought to assess (1) clinical characteristics
including serum biomarkers: high sensitivity troponin T (hsTnT) and N-terminal prohormone
brain natriuretic peptide (NT-proBNP) in clinically stable cardiolaminopathy patients, and (2)
outcome among pathogenic/likely pathogenic lamin A/C gene (LMNA) mutation carriers. Our …
unclear whether circulating cardiac biomarkers are helpful in the detection and risk
assessment of cardiolaminopathies. We sought to assess (1) clinical characteristics
including serum biomarkers: high sensitivity troponin T (hsTnT) and N-terminal prohormone
brain natriuretic peptide (NT-proBNP) in clinically stable cardiolaminopathy patients, and (2)
outcome among pathogenic/likely pathogenic lamin A/C gene (LMNA) mutation carriers. Our …
Mutations in the lamin A/C gene are variably phenotypically expressed; however, it is unclear whether circulating cardiac biomarkers are helpful in the detection and risk assessment of cardiolaminopathies. We sought to assess (1) clinical characteristics including serum biomarkers: high sensitivity troponin T (hsTnT) and N-terminal prohormone brain natriuretic peptide (NT-proBNP) in clinically stable cardiolaminopathy patients, and (2) outcome among pathogenic/likely pathogenic lamin A/C gene (LMNA) mutation carriers. Our single-centre cohort included 53 patients from 21 families. Clinical, laboratory, follow-up data were analysed. Median follow-up was 1522 days. The earliest abnormality, emerging in the second and third decades of life, was elevated hsTnT (in 12% and in 27% of patients, respectively), followed by the presence of atrioventricular block, heart failure, and malignant ventricular arrhythmia (MVA). In patients with missense vs. other mutations, we found no difference in MVA occurrence and, surprisingly, worse transplant-free survival. Increased levels of both hsTnT and NT-proBNP were strongly associated with MVA occurrence (HR > 13, p ≤ 0.02 in both) in univariable analysis. In multivariable analysis, NT-proBNP level > 150 pg/mL was the only independent indicator of MVA. We conclude that assessment of circulating cardiac biomarkers may help in the detection and risk assessment of cardiolaminopathies.
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