Evidence map›Paper›PMID 37466864›Full record

ArticlePediatric nephrology (Berlin, Germany)2023

Associations between collagen X biomarker and linear growth velocity in a pediatric chronic kidney disease cohort.

Denver D Brown, Jennifer Roem, Derek K Ng, Ryan F Coghlan, Brian Johnstone, William Horton, Susan L Furth, Bradley A Warady, Michal L Melamed, Andrew Dauber and 1 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00327860 (Chronic Kidney Disease in Children Prospective Cohort Study), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 38% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00327860 recruitingnot on this map

Chronic Kidney Disease in Children Prospective Cohort Study (CKiD)

TypeobservationalSponsorJohns Hopkins Bloomberg School of Public HealthRan2003 to 2028Enrolled1,300ConditionsChronic Kidney Disease
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Denver D BrownDivision of Nephrology, Children's National Hospital/Department of Pediatrics, George Washington School of Medicine, 111 Michigan Ave, Washington, NWDC, USA. ddbrown@childrensnational.org.ORCID http://orcid.org/0000-0003-3381-0336
Jennifer RoemJohns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Derek K NgJohns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Ryan F CoghlanResearch Center, Shriners Hospital for Children, Portland, OR, USA.
Brian JohnstoneResearch Center, Shriners Hospital for Children, Portland, OR, USA.
William HortonResearch Center, Shriners Hospital for Children, Portland, OR, USA.
Susan L FurthDivision of Pediatric Nephrology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Bradley A WaradyDivision of Pediatric Nephrology, Children's Mercy Hospital, Kansas City, MO, USA.
Michal L MelamedDepartment of Medicine, Albert Einstein College of Medicine, Bronx, NY, USA.
Andrew DauberDivision of Endocrinology, Children's National Hospital/Department of Pediatrics, George Washington School of Medicine, Washington, DC, USA.
CKiD Study Investigators
Johns Hopkins University · USChildren's Mercy Hospital · USChildren's Hospital of Philadelphia · USChildren's National · USOregon Health & Science University · USAlbert Einstein College of Medicine · USShriners Hospitals for Children - Portland · US

Funding

Chronic Kidney Disease in Children Study (C-Kid)U01DK066174 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SUSAN L. FURTH · 2003 to 2026
$25.1M
CKiD Cardiovascular Testing Travel SupplementU01DK066143 · NIDDK · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI Bradley Alan Warady · 2003 to 2026
$24.2M
The Kidney Disease in Children Data Management and Analysis Center (KIDMAC)U24DK066116 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI Derek K Ng · 2018 to 2026
$12.6M
Child Health Research Career Development Award (CHRCDA) Program at Children's NationalK12HD001399 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI NATHAN KUPPERMANN · 2001 to 2026
$9.1M
MOLECULAR MECHANISMS OF DYSMORPHOLOGYZ01HD000139 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI PORTER, FORBES DENNISON · 1997 to 2008
$2.8M
Central Biochemistry Laboratory of the CKID ConsortiumU24DK082194 · NIDDK · UNIVERSITY OF ROCHESTER · PI SCHWARTZ, GEORGE J · 2018 to 2022
$1.7M
Intramural NIH HHS Z01 HD000139NICHD NIH HHS K12 HD001399NIDDK NIH HHS U01 DK066143NIDDK NIH HHS U01 DK066174NIDDK NIH HHS U24 DK066116NIDDK NIH HHS U24 DK082194
6 · The paper itself

Abstract

backgroundCollagen 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.

methodsWe 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.

resultsA 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.

conclusionsCXM 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.

Indexed as

Renal Insufficiency, ChronicAdolescentBiomarkersChildCollagenFemaleHumansMaleProteinuriaBiomarkersCollagenBiomarkerCKDCXMGrowthPediatrics

Identifiers

PMID37466864
PMCPMC10642619
OpenAlexW4384663845

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.