Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease (Apr 2025)

Progression of Carotid Intima‐Media Thickness in Children of the Cardiovascular Comorbidity in Children With Chronic Kidney Disease Study: Risk Factors and Impact of Blood Pressure Dynamics

  • Anke Doyon,
  • Jonas Hofstetter,
  • Aysun Karabay Bayazit,
  • Karolis Azukaitis,
  • Ana Niemirska,
  • Mahmut Civilibal,
  • Ipek Kaplan Bulut,
  • Ali Duzova,
  • Berna Oguz,
  • Bruno Ranchin,
  • Rukshana Shroff,
  • Yelda Bilginer,
  • Salim Caliskan,
  • Dusan Paripovic,
  • Cengiz Candan,
  • Alev Yilmaz,
  • Jerome Harambat,
  • Zeynep Birsin Özçakar,
  • Francesca Lugani,
  • Harika Alpay,
  • Sibylle Tschumi,
  • Ebru Yilmaz,
  • Dorota Drozdz,
  • Yilmaz Tabel,
  • Gül Özcelik,
  • Alberto Caldas Afonso,
  • Onder Yavascan,
  • Anette Melk,
  • Uwe Querfeld,
  • Franz Schaefer

DOI
https://doi.org/10.1161/jaha.124.037563
Journal volume & issue
Vol. 14, no. 7

Abstract

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Background Carotid intima‐media thickness (cIMT) may identify early alterations in the vascular phenotype in children with chronic kidney disease (CKD). Methods and Results Investigation of longitudinal changes in cIMT SD scores (SDS) in 670 patients from the 4C Study (Cardiovascular Comorbidity in Children With CKD Study), aged 6 to 17 years, with CKD stage 3 to 5 at baseline. The longitudinal trajectory of cIMT SDS over up to 8 years was examined using a longitudinal mixed‐effects model. The yearly progression rate in cIMT SDS (β=0.20 [95% CI, 0.13–0.28]) remained positive during the initial 4.5‐year follow‐up period but slowed down quadratically with increasing observation time (β=−0.02 [95% CI, −0.03 to −0.01]). Risk factors for increased cIMT SDS included time since baseline, younger age, higher height SDS, female sex, elevated diastolic blood pressure, and lower serum albumin, but not estimated glomerular filtration rate. In patients with progressive CKD, higher albuminuria was additionally associated with an increase in cIMT SDS. In patients with stable CKD, serum phosphate and time were the only risk factors identified for elevated cIMT SDS. Annual rates of change in blood pressure were positively correlated with the rate of change in cIMT SDS within the first 4.5 years (for systolic: β=0.42 [95% CI, 0.22–0.62]; for diastolic: β=1.56 [95% CI, 1.01–2.11]). Conclusions The results show a significant longitudinal increase in cIMT SDS in children with CKD. Changes in blood pressure are associated with the progression of cIMT SDS, suggesting a relevant impact of blood pressure modulation on cIMT SDS.

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