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Associations between collagen X biomarker and linear growth velocity in a pediatric chronic kidney disease cohort.
Brown, Denver D; Roem, Jennifer; Ng, Derek K; Coghlan, Ryan F; Johnstone, Brian; Horton, William; Furth, Susan L; Warady, Bradley A; Melamed, Michal L; Dauber, Andrew.
Afiliação
  • Brown DD; Division of Nephrology, Children's National Hospital/Department of Pediatrics, George Washington School of Medicine, 111 Michigan Ave, Washington, NWDC, USA. ddbrown@childrensnational.org.
  • Roem J; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Ng DK; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Coghlan RF; Research Center, Shriners Hospital for Children, Portland, OR, USA.
  • Johnstone B; Research Center, Shriners Hospital for Children, Portland, OR, USA.
  • Horton W; Department of Orthopaedics & Rehabilitation, Oregon Health & Science University, Portland, OR, USA.
  • Furth SL; Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Warady BA; Research Center, Shriners Hospital for Children, Portland, OR, USA.
  • Melamed ML; Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR, USA.
  • Dauber A; Division of Pediatric Nephrology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Pediatr Nephrol ; 38(12): 4145-4156, 2023 12.
Article em En | MEDLINE | ID: mdl-37466864
ABSTRACT

BACKGROUND:

Collagen X biomarker (CXM) is a novel biomarker of linear growth velocity. We investigated whether CXM correlated with measured growth velocity in children with impaired kidney function.

METHODS:

We used data from children aged 2 through 16 years old enrolled in the Chronic Kidney Disease in Children (CKiD) study. We assessed the association between CXM level and growth velocity based on height measurements obtained at study visits using linear regression models constructed separately by sex, with and without adjustment for CKD covariates. Linear mixed-effects models were used to capture the between-individual and within-individual CXM changes over time associated with concomitant changes in growth velocity from baseline through follow-up.

RESULTS:

A total of 967 serum samples from 209 participants were assayed for CXM. CXM correlated more strongly in females compared to male participants. After adjustment for growth velocity and CKD covariates, only proteinuria in male participants affected CXM levels. Finally, we quantified the between- and within-participant associations between CXM level and growth velocity. A between-participant increase of 24% and 15% in CXM level in females and males, respectively, correlated with a 1 cm/year higher growth velocity. Within an individual participant, on average, 28% and 13% increases in CXM values in females and males, respectively, correlated with a 1 cm/year change in measured growth.

CONCLUSIONS:

CXM measurement is potentially a valuable aid for monitoring growth in pediatric CKD. However, future research, including studies of CXM metabolism, is needed to clarify whether CXM can be a surrogate of growth in children with CKD. A higher resolution version of the Graphical abstract is available as Supplementary information.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Tipo de estudo: Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Insuficiência Renal Crônica Tipo de estudo: Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article