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Gut microbiota, endotoxemia, inflammation, and oxidative stress in patients with heart failure, left ventricular assist device, and transplant.
Yuzefpolskaya, Melana; Bohn, Bruno; Nasiri, Mojdeh; Zuver, Amelia M; Onat, Drew D; Royzman, Eugene A; Nwokocha, Joseph; Mabasa, Melissa; Pinsino, Alberto; Brunjes, Danielle; Gaudig, Antonia; Clemons, Autumn; Trinh, Pauline; Stump, Stephania; Giddins, Marla J; Topkara, Veli K; Garan, A Reshad; Takeda, Koji; Takayama, Hiroo; Naka, Yoshifumi; Farr, Maryjane A; Nandakumar, Renu; Uhlemann, Anne-Catrin; Colombo, Paolo C; Demmer, Ryan T.
Afiliação
  • Yuzefpolskaya M; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Bohn B; Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota.
  • Nasiri M; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Zuver AM; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Onat DD; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Royzman EA; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Nwokocha J; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Mabasa M; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Pinsino A; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Brunjes D; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Gaudig A; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Clemons A; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Trinh P; Department of Environmental and Occupational Health Sciences, University of Washington, School of Public Health, Seattle, Washington.
  • Stump S; Department of Medicine, Division of Infectious Diseases and Microbiome and Pathogen Genomics Core, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Giddins MJ; Department of Medicine, Division of Infectious Diseases and Microbiome and Pathogen Genomics Core, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Topkara VK; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Garan AR; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Takeda K; Division of Cardiothoracic Surgery, Department of Surgery, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Takayama H; Division of Cardiothoracic Surgery, Department of Surgery, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Naka Y; Division of Cardiothoracic Surgery, Department of Surgery, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Farr MA; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Nandakumar R; Biomarkers Core Laboratory, Irving Institute for Clinical and Translational Research, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Uhlemann AC; Department of Medicine, Division of Infectious Diseases and Microbiome and Pathogen Genomics Core, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Colombo PC; Division of Cardiology, Department of Medicine, New York Presbyterian Hospital, Columbia University, New York City, New York.
  • Demmer RT; Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota; Division of Epidemiology, Mailman School of Public Health, Columbia University, New York City, New York. Electronic address: demm0009@umn.edu.
J Heart Lung Transplant ; 39(9): 880-890, 2020 09.
Article em En | MEDLINE | ID: mdl-32139154
ABSTRACT

BACKGROUND:

Gut microbial imbalance may contribute to endotoxemia, inflammation, and oxidative stress in heart failure (HF). Changes occurring in the intestinal microbiota and inflammatory/oxidative milieu during HF progression and following left ventricular assist device (LVAD) or heart transplantation (HT) are unknown. We aimed to investigate variation in gut microbiota and circulating biomarkers of endotoxemia, inflammation, and oxidative stress in patients with HF (New York Heart Association, Class I-IV), LVAD, and HT.

METHODS:

We enrolled 452 patients. Biomarkers of endotoxemia (lipopolysaccharide and soluble [sCD14]), inflammation (C-reactive protein, interleukin-6, tumor necrosis factor-α, and endothelin-1 adiponectin), and oxidative stress (isoprostane) were measured in 644 blood samples. A total of 304 stool samples were analyzed using 16S rRNA sequencing.

RESULTS:

Gut microbial community measures of alpha diversity were progressively lower across worsening HF class and were similarly reduced in patients with LVAD and HT (p < 0.05). Inflammation and oxidative stress were elevated in patients with Class IV HF vs all other groups (all p < 0.05). Lipopolysaccharide was elevated in patients with Class IV HF (vs Class I-III) as well as in patients with LVAD and HT (p < 0.05). sCD14 was elevated in patients with Class IV HF and LVAD (vs Class I-III, p < 0.05) but not in patients with HT.

CONCLUSIONS:

Reduced gut microbial diversity and increased endotoxemia, inflammation, and oxidative stress are present in patients with Class IV HF. Inflammation and oxidative stress are lower among patients with LVAD and HT relative to patients with Class IV HF, whereas reduced gut diversity and endotoxemia persist in LVAD and HT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coração Auxiliar / Transplante de Coração / Endotoxemia / Microbioma Gastrointestinal / Insuficiência Cardíaca / Ventrículos do Coração / Inflamação Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coração Auxiliar / Transplante de Coração / Endotoxemia / Microbioma Gastrointestinal / Insuficiência Cardíaca / Ventrículos do Coração / Inflamação Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article