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Vitamin D and its associations with blood pressure in the Chronic Kidney Disease in Children (CKiD) cohort.
Kumar, Juhi; Roem, Jennifer; Furth, Susan L; Warady, Bradley A; Atkinson, Meredith A; Flynn, Joseph T.
Affiliation
  • Kumar J; Department of Pediatrics, University of Pittsburgh Medical Center/Children's Hospital of Pittsburgh, Pittsburgh, PA, USA. Kumarj3@upmc.edu.
  • Roem J; Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
  • Furth SL; Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Warady BA; Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO, USA.
  • Atkinson MA; Department of Pediatrics, Johns Hopkins Medicine, Baltimore, MD, USA.
  • Flynn JT; Department of Pediatrics, Seattle Children's Hospital, Seattle, WA, USA.
Pediatr Nephrol ; 2024 Jul 06.
Article de En | MEDLINE | ID: mdl-38970659
ABSTRACT

BACKGROUND:

Vitamin D (25OHD) can modulate pathways and mechanisms that regulate blood pressure (BP). Observational studies in children and adults have shown an inverse association between 25OHD and BP. Studies evaluating associations between 25OHD and BP in pediatric chronic kidney disease are limited.

METHODS:

We evaluated the associations between 25OHD and BP using data from the Chronic Kidney Disease in Children (CKiD) study. Clinic or ambulatory BP index was defined as participant's BP divided by 95th age-sex-height-specific BP percentile, an index > 1 suggests hypertension. Primary outcomes of interest were changes in systolic and diastolic clinic and ambulatory BP indices over follow-up. Linear mixed-effects models were used to evaluate associations between BP indices and 25OHD.

RESULTS:

The study cohort consisted of 370 participants who contributed 970 person-visits. A subset of 194 participants with ambulatory BP data contributed 465 person-visits. There was an association between baseline 25OHD levels and clinic systolic BP index such that for every 10 ng/ml lower 25OHD, clinic systolic BP index was 1.0% higher (95%CI 0.2-1.8, p = 0.016) between participants. The association between clinic diastolic BP index with baseline 25OHD was not significant. For within-person changes, longitudinal decreases in 25OHD were not significantly associated with concomitant increases in clinic systolic or diastolic BP index. There were no significant associations between 25OHD levels at baseline or longitudinally with 24-h ABPM indices.

CONCLUSIONS:

Low 25OHD levels were associated with higher clinic systolic BP in children with CKD. Vitamin D supplementation to maintain normal 25OHD levels might be a useful adjunctive treatment in optimizing BP control in these high-risk patients.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pediatr Nephrol Sujet du journal: NEFROLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Pediatr Nephrol Sujet du journal: NEFROLOGIA / PEDIATRIA Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique