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DOI 10.1016/j.healun.2018.03.006

Медицинская библиотека · The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2018

Clinical phenomapping and outcomes after heart transplantation.

Bakir Maral, Jackson Nicholas J, Han Simon X, Bui Alex, Chang Eleanor, Liem David A, Ardehali Abbas, Ardehali Reza, Baas Arnold S, Press Marcella Calfon, Cruz Daniel, Deng Mario C, DePasquale Eugene C, Fonarow Gregg C, Khuu Tam, Kwon Murray H, Kubak Bernard M, Nsair Ali, Phung Jennifer L, Reed Elaine F, Schaenman Joanna M, Shemin Richard J, Zhang Qiuheng J, Tseng Chi-Hong, Cadeiras Martin

СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Survival after heart transplantation (HTx) is limited by complications related to alloreactivity, immune suppression, and adverse effects of pharmacologic therapies. We hypothesize that time-dependent phenomapping of clinical and molecular data sets is a valuable approach to clinical assessments and guiding medical management to improve outcomes.

METHODS

We analyzed clinical, therapeutic, biomarker, and outcome data from 94 adult HTx patients and 1,557 clinical encounters performed between January 2010 and April 2013. Multivariate analyses were used to evaluate the association between immunosuppression therapy, biomarkers, and the combined clinical end point of death, allograft loss, retransplantation, and rejection. Data were analyzed by K-means clustering (K = 2) to identify patterns of similar combined immunosuppression management, and percentile slopes were computed to examine the changes in dosages over time. Findings were correlated with clinical parameters, human leucocyte antigen antibody titers, and peripheral blood mononuclear cell gene expression of the AlloMap (CareDx, Inc., Brisbane, CA) test genes. An intragraft, heart tissue gene coexpression network analysis was performed.

RESULTS

Unsupervised cluster analysis of immunosuppressive therapies identified 2 groups, 1 characterized by a steeper immunosuppression minimization, associated with a higher likelihood for the combined end point, and the other by a less pronounced change. A time-dependent phenomap suggested that patients in the group with higher event rates had increased human leukocyte antigen class I and II antibody titers, higher expression of the FLT3 AlloMap gene, and lower expression of the MARCH8 and WDR40A AlloMap genes. Intramyocardial biomarker-related coexpression network analysis of the FLT3 gene showed an immune system-related network underlying this biomarker.

CONCLUSIONS

Time-dependent precision phenotyping is a mechanistically insightful, data-driven approach to characterize patterns of clinical care and identify ways to improve clinical management and outcomes.

Для цитирования: Bakir Maral, Jackson Nicholas J, Han Simon X, Bui Alex, Chang Eleanor, Liem David A, Ardehali Abbas, Ardehali Reza, Baas Arnold S, Press Marcella Calfon, Cruz Daniel, Deng Mario C, DePasquale Eugene C, Fonarow Gregg C, Khuu Tam, Kwon Murray H, Kubak Bernard M, Nsair Ali, Phung Jennifer L, Reed Elaine F, Schaenman Joanna M, Shemin Richard J, Zhang Qiuheng J, Tseng Chi-Hong, Cadeiras Martin. Clinical phenomapping and outcomes after heart transplantation.. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 2018. DOI: 10.1016/j.healun.2018.03.006.

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