Association between anemia and renal prognosis in autosomal dominant polycystic kidney disease: a retrospective study.
Adult
Anemia
/ blood
Disease Progression
Female
Glomerular Filtration Rate
Hemoglobins
/ metabolism
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Mutation
Polycystic Kidney, Autosomal Dominant
/ complications
Prognosis
Proportional Hazards Models
Retrospective Studies
Sex Factors
TRPP Cation Channels
/ genetics
Anemia
Autosomal dominant polycystic kidney disease
Kidney disease progression
Prognosis
Renal replacement therapy
Journal
Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
17
09
2019
accepted:
22
01
2020
pubmed:
10
2
2020
medline:
10
3
2021
entrez:
10
2
2020
Statut:
ppublish
Résumé
Though anemia is a sign of poor renal prognosis in chronic kidney disease (CKD), hemoglobin (Hb) levels are typically higher in autosomal dominant polycystic kidney disease (ADPKD) than in other kidney diseases, and anemia has not been examined as a potential prognosticator. Thus, we investigated anemia as a factor for renal prognosis in ADPKD. In total, 115 non-dialysis patients, 48 men and 67 women, with ADPKD were evaluated. The renal outcome of a 50% reduction in the estimated glomerular filtration rate or renal replacement therapy was examined using the Cox regression analysis and Kaplan-Meier analysis. Patients were followed for a median of 5.5 years and 50 patients had reached the end point. The mean age of the patients at the first visit was 45.9 ± 13.3 years. The overall mean Hb was 12.90 ± 1.85 g/dL, and the mean Hb in men and women was 13.82 ± 1.72 g/dL and 12.25 ± 1.65 g/dL, respectively. Hb levels and uric protein content were statistically significant factors for poor renal prognosis, while hypertension and genetic mutations failed to reach significance. Furthermore, statistical significance was found in men with Hb < 12 g/dL and in women with Hb < 11 g/dL. Anemia had significant association with kidney disease progression in patients with ADPKD. We found that anemia might be a factor for poor renal prognosis in ADPKD. Furthermore, a sex difference was found, wherein men with Hb < 12 g/dL and women with Hb < 11 g/dL were at risk of renal disease progression.
Sections du résumé
BACKGROUND
BACKGROUND
Though anemia is a sign of poor renal prognosis in chronic kidney disease (CKD), hemoglobin (Hb) levels are typically higher in autosomal dominant polycystic kidney disease (ADPKD) than in other kidney diseases, and anemia has not been examined as a potential prognosticator. Thus, we investigated anemia as a factor for renal prognosis in ADPKD.
METHODS
METHODS
In total, 115 non-dialysis patients, 48 men and 67 women, with ADPKD were evaluated. The renal outcome of a 50% reduction in the estimated glomerular filtration rate or renal replacement therapy was examined using the Cox regression analysis and Kaplan-Meier analysis.
RESULTS
RESULTS
Patients were followed for a median of 5.5 years and 50 patients had reached the end point. The mean age of the patients at the first visit was 45.9 ± 13.3 years. The overall mean Hb was 12.90 ± 1.85 g/dL, and the mean Hb in men and women was 13.82 ± 1.72 g/dL and 12.25 ± 1.65 g/dL, respectively. Hb levels and uric protein content were statistically significant factors for poor renal prognosis, while hypertension and genetic mutations failed to reach significance. Furthermore, statistical significance was found in men with Hb < 12 g/dL and in women with Hb < 11 g/dL. Anemia had significant association with kidney disease progression in patients with ADPKD.
CONCLUSIONS
CONCLUSIONS
We found that anemia might be a factor for poor renal prognosis in ADPKD. Furthermore, a sex difference was found, wherein men with Hb < 12 g/dL and women with Hb < 11 g/dL were at risk of renal disease progression.
Identifiants
pubmed: 32036465
doi: 10.1007/s10157-020-01856-1
pii: 10.1007/s10157-020-01856-1
doi:
Substances chimiques
Hemoglobins
0
TRPP Cation Channels
0
polycystic kidney disease 1 protein
0
polycystic kidney disease 2 protein
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM