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Skeletal Muscle Adiposity and Lung Function Trajectory in the Severe Asthma Research Program.
Tattersall, Matthew C; Lee, Kristine E; Tsuchiya, Nanae; Osman, Fauzia; Korcarz, Claudia E; Hansen, Kristin M; Peters, Michael C; Fahy, John V; Longhurst, Colin A; Dunican, Eleanor; Wentzel, Sally E; Leader, Joseph K; Israel, Elliot; Levy, Bruce D; Castro, Mario; Erzurum, Serpil C; Lempel, Jason; Moore, Wendy C; Bleecker, Eugene R; Phillips, Brenda R; Mauger, David T; Hoffman, Eric A; Fain, Sean B; Reeder, Scott B; Sorkness, Ron L; Jarjour, Nizar N; Denlinger, Loren C; Schiebler, Mark L.
Afiliação
  • Tattersall MC; Division of Cardiology.
  • Lee KE; Department of Medicine.
  • Tsuchiya N; Department of Biostatistics, and.
  • Osman F; Division of Cardiothoracic Imaging, Department of Radiology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin.
  • Korcarz CE; Department of Radiology, School of Medicine, University of the Ryukyus, Nishihara, Japan.
  • Hansen KM; Department of Medicine.
  • Peters MC; Division of Cardiology.
  • Fahy JV; Department of Medicine.
  • Longhurst CA; Division of Cardiology.
  • Dunican E; Department of Medicine.
  • Wentzel SE; Division of Pulmonary and Critical Care, Department of Medicine, University of California, San Francisco, San Francisco, California.
  • Leader JK; Division of Pulmonary and Critical Care, Department of Medicine, University of California, San Francisco, San Francisco, California.
  • Israel E; Department of Medicine.
  • Levy BD; Department of Medicine, School of Medicine, University College Dublin, Dublin, Ireland.
  • Castro M; St. Vincent's Hospital Elm Park, Dublin, Ireland.
  • Erzurum SC; Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, and.
  • Lempel J; Department of Radiology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Moore WC; Division of Pulmonary and Critical Care and.
  • Bleecker ER; Division of Allergy and Immunology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Phillips BR; Division of Pulmonary and Critical Care and.
  • Mauger DT; Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Kansas Medical Center, Kansas City, Kansas.
  • Hoffman EA; Lerner Research Institute, Cleveland, Ohio.
  • Fain SB; Department of Radiology, Cleveland Clinic Foundation, Cleveland, Ohio.
  • Reeder SB; Section of Pulmonary, Critical Care, Allergy and Immunologic Diseases, Department of Internal Medicine, School of Medicine, Wake Forest University, Winston-Salem, North Carolina.
  • Sorkness RL; Division of Genetics and.
  • Jarjour NN; Division of Pharmacokinetics, Department of Medicine, College of Medicine, University of Arizona, Tucson, Arizona.
  • Denlinger LC; Department of Public Health Sciences, College of Medicine, Pennsylvania State University, Hershey, Pennsylvania; and.
  • Schiebler ML; Department of Public Health Sciences, College of Medicine, Pennsylvania State University, Hershey, Pennsylvania; and.
Am J Respir Crit Care Med ; 207(4): 475-484, 2023 02 15.
Article em En | MEDLINE | ID: mdl-36194556
Rationale: Extrapulmonary manifestations of asthma, including fatty infiltration in tissues, may reflect systemic inflammation and influence lung function and disease severity. Objectives: To determine if skeletal muscle adiposity predicts lung function trajectory in asthma. Methods: Adult SARP III (Severe Asthma Research Program III) participants with baseline computed tomography imaging and longitudinal postbronchodilator FEV1% predicted (median follow-up 5 years [1,132 person-years]) were evaluated. The mean of left and right paraspinous muscle density (PSMD) at the 12th thoracic vertebral body was calculated (Hounsfield units [HU]). Lower PSMD reflects higher muscle adiposity. We derived PSMD reference ranges from healthy control subjects without asthma. A linear multivariable mixed-effects model was constructed to evaluate associations of baseline PSMD and lung function trajectory stratified by sex. Measurements and Main Results: Participants included 219 with asthma (67% women; mean [SD] body mass index, 32.3 [8.8] kg/m2) and 37 control subjects (51% women; mean [SD] body mass index, 26.3 [4.7] kg/m2). Participants with asthma had lower adjusted PSMD than control subjects (42.2 vs. 55.8 HU; P < 0.001). In adjusted models, PSMD predicted lung function trajectory in women with asthma (ß = -0.47 Δ slope per 10-HU decrease; P = 0.03) but not men (ß = 0.11 Δ slope per 10-HU decrease; P = 0.77). The highest PSMD tertile predicted a 2.9% improvement whereas the lowest tertile predicted a 1.8% decline in FEV1% predicted among women with asthma over 5 years. Conclusions: Participants with asthma have lower PSMD, reflecting greater muscle fat infiltration. Baseline PSMD predicted lung function decline among women with asthma but not men. These data support an important role of metabolic dysfunction in lung function decline.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Pulmão Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Respir Crit Care Med Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Pulmão Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Respir Crit Care Med Ano de publicação: 2023 Tipo de documento: Article