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Evaluating immune response and metabolic related biomarkers pre-allogenic hematopoietic stem cell transplant in acute myeloid leukemia.
Siamakpour-Reihani, Sharareh; Cao, Felicia; Lyu, Jing; Ren, Yi; Nixon, Andrew B; Xie, Jichun; Bush, Amy T; Starr, Mark D; Bain, James R; Muehlbauer, Michael J; Ilkayeva, Olga; Byers Kraus, Virginia; Huebner, Janet L; Chao, Nelson J; Sung, Anthony D.
Afiliação
  • Siamakpour-Reihani S; Division of Hematologic Malignancies and Cellular Therapy, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Cao F; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Lyu J; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Ren Y; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Nixon AB; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Xie J; Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Bush AT; Division of Hematologic Malignancies and Cellular Therapy, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Starr MD; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Bain JR; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Muehlbauer MJ; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Ilkayeva O; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Byers Kraus V; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Huebner JL; Department of Medicine, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Chao NJ; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
  • Sung AD; Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, North Carolina, United States of America.
PLoS One ; 17(6): e0268963, 2022.
Article em En | MEDLINE | ID: mdl-35700185
Although hematopoietic stem cell transplantation (HCT) is the only curative treatment for acute myeloid leukemia (AML), it is associated with significant treatment related morbidity and mortality. There is great need for predictive biomarkers associated with overall survival (OS) and clinical outcomes. We hypothesized that circulating metabolic, inflammatory, and immune molecules have potential as predictive biomarkers for AML patients who receive HCT treatment. This retrospective study was designed with an exploratory approach to comprehensively characterize immune, inflammatory, and metabolomic biomarkers. We identified patients with AML who underwent HCT and had existing baseline plasma samples. Using those samples (n = 34), we studied 65 blood based metabolomic and 61 immune/inflammatory related biomarkers, comparing patients with either long-term OS (≥ 3 years) or short-term OS (OS ≤ 1 years). We also compared the immune/inflammatory response and metabolomic biomarkers in younger vs. older AML patients (≤30 years vs. ≥ 55 years old). In addition, the biomarker profiles were analyzed for their association with clinical outcomes, namely OS, chronic graft versus host disease (cGVHD), acute graft versus host disease (aGVHD), infection and relapse. Several baseline biomarkers were elevated in older versus younger patients, and baseline levels were lower for three markers (IL13, SAA, CRP) in patients with OS ≥ 3 years. We also identified immune/inflammatory response markers associated with aGVHD (IL-9, Eotaxin-3), cGVHD (Flt-1), infection (D-dimer), or relapse (IL-17D, bFGF, Eotaxin-3). Evaluation of metabolic markers demonstrated higher baseline levels of medium- and long-chain acylcarnitines (AC) in older patients, association with aGVHD (lactate, long-chain AC), and cGVHD (medium-chain AC). These differentially expressed profiles merit further evaluation as predictive biomarkers.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Doença Enxerto-Hospedeiro Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos