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Racial differences in serological markers across the first year of injury in spinal cord injury: a retrospective analysis of a multi-center interventional study.
Li, Jia; Farrow, Matthew; Ibrahim, Kerollos; McTigue, Dana M; Kramer, John; Tong, Bobo; Jutzeler, Catherine; Jones, Linda; Yarar-Fisher, Ceren.
Afiliação
  • Li J; College of Medicine, Department of Physical Medicine & Rehabilitation, The Ohio State University, Columbus, OH, USA. Jia.Li@osumc.edu.
  • Farrow M; College of Medicine, Department of Physical Medicine & Rehabilitation, The Ohio State University, Columbus, OH, USA.
  • Ibrahim K; College of Medicine, Florida State University, Tallahassee, FL, USA.
  • McTigue DM; College of Medicine - Department of Neuroscience, The Ohio State University, Columbus, OH, USA.
  • Kramer J; International Collaboration on Repair Discoveries (ICORD), University of British Columbia, Vancouver, BC, Canada.
  • Tong B; International Collaboration on Repair Discoveries (ICORD), University of British Columbia, Vancouver, BC, Canada.
  • Jutzeler C; Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.
  • Jones L; Department of Physical Therapy, Thomas Jefferson University, Philadelphia, PA, USA.
  • Yarar-Fisher C; College of Medicine, Department of Physical Medicine & Rehabilitation, The Ohio State University, Columbus, OH, USA.
Spinal Cord ; 2024 Jul 03.
Article em En | MEDLINE | ID: mdl-38961159
ABSTRACT
STUDY

DESIGN:

Secondary analysis of a randomized, multi-center, placebo-controlled study(Sygen®).

OBJECTIVES:

To evaluate racial differences in serological markers in individuals with spinal cord injury(SCI) across the first year of injury.

SETTING:

Hospitals in North America.

METHODS:

Serological markers (e.g.,cell count, liver, kidney, and pancreatic function, metabolism, and muscle damage) were assessed among 316 participants (247 White, 69 Black) at admission, weeks 1, 2, 4, 8, and 52 post-injury. Linear mixed models were employed to explore the main effects of time, race (Black vs. White), and their interaction, with adjustment of covariates such as study center, polytrauma, injury (level, completeness), treatment group, and sex.

RESULTS:

A main effect of race was observed where White individuals had higher alanine transaminase, blood urea nitrogen(BUN), BUN/Creatinine ratio, sodium, and chloride, while Black individuals had higher calcium, total serum protein, and platelets. For markers with interaction effects, post-hoc comparisons showed that at week 52, White individuals had higher mature neutrophils, hematocrit, hemoglobin, mean corpuscular hemoglobin, albumin, and triglycerides, and Black individuals had higher amylase. Eosinophils, monocytes, red blood cells, aspartate aminotransferase, bilirubin, cholesterol, partial thromboplastin time, urine specific gravity, urine pH, CO2, and inorganic phosphorus did not differ between races.

CONCLUSIONS:

Our results revealed racial differences in serological markers and underscores the importance of considering race as a determinant of physiological responses. Future studies are warranted to explore the causes and implications of these racial disparities to facilitate tailored clinical management and social policy changes that can improve health equity.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Spinal Cord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Spinal Cord Assunto da revista: NEUROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos