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akaturk Akademik ölçüm

Makale detayı · 2025 · article

Comparative validation of the Mayo Clinic imaging classification and PROPKD score for predicting ADPKD progression across diverse ethnic cohorts

Dergi Journal of Nephrology
ISSN10.1007/s40620-025-02282-w
YÖKSİS OpenAlex
Yıl2025
Atıf3OpenAlex
Yüzdelik%86,8
FWCI2,271,00 = dünya ortalaması
Scopus (SJR)Q2
WoS (JCR)Q2

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıJournal of Nephrology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

OpenAlex İngilizce

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of end-stage kidney disease (ESKD). In this retrospective multicenter cohort study, we aimed to evaluate the concordance, sensitivity and specificity of the predictive abilities of the Mayo Clinic Imaging Class (MCIC) and Predicting Renal Outcome in Polycystic Kidney Disease (PROPKD) score for progression to ESKD. METHODS: more than 1 month apart and/or (2) initiation of kidney replacement therapy. RESULTS: One hundred eighty-seven ADPKD patients with PKD1 or PKD2 variants were included, with the majority identifying as White (93%), followed by Black (6%) and Hispanic (0.5%). The PROPKD score showed moderate ability (AUC = 0.702) to predict progression to ESKD, performing better in Black patients (AUC = 0.800) than in White patients (AUC = 0.764). However, the predictive accuracy declined (AUC = 0.644) when the PROPKD score was categorized into risk levels (low, intermediate, high). The MCIC showed lower ability (AUC = 0.578) to predict progression to ESKD than the PROPKD score. Using LASSO regularization and multivariable Cox regression, self-identified Black ethnicity [HR = 12.24 (95% CI: 3.19-46.94, p < 0.001)] and age at initial follow-up [HR = 1.05 (95% CI:1.01-1.09, p = 0.007)] emerged as significant predictors of progression to ESKD. CONCLUSIONS: The PROPKD score appears to be a useful tool for predicting ADPKD progression across various ethnic groups, with self-identified Black ethnicity and age at initial follow-up emerging as key predictors of kidney failure.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

3atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 7 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  2. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  3. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  4. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  5. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  6. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex
  7. 2025 Evaluating gene variations in autosomal dominant polycystic kidney disease patients using whole exome sequencing and phenotype to genotype analysisAtıf 0 · OpenAlex

Yazarlar

11
  1. Yaşar Çalışkan 1
  2. ABDULMECİT YILDIZ 2
  3. HANDE AYPEK 3
  4. Özgür Oto 4
  5. Cuma Gül 5
  6. ALPARSLAN DEMİRAY 6
  7. GÜLŞAH ÇEÇENER BURSA ULUDAĞ ÜNİVERSİTESİ 7
  8. Yiğit Kurtuluş 8
  9. Bahar Bastani 9
  10. Krista Lentine 10
  11. İSMAİL KOÇYİĞİT 11