Abstract | BACKGROUND: METHODS: We searched Medline, Embase, Science Citation Index, Cochrane Central Register of Controlled Trials, and Clinical Trial Registries for randomized controlled trials comparing daprodustat with placebo for anemic patients with CKD. RESULTS: Four studies were included. Compared with placebo groups, daprodustat groups significantly increased hemoglobin (WMD 1.29 g/dL; 95% CI 0.96-1.62, p < 0.00001), transferrin (WMD 0.67 g/dL; 95% CI 0.45-0.89, p < 0.00001), and total iron binding capacity (WMD 9.97 g/dL; 95% CI 6.07-13.8, p < 0.00001). Daprodustat groups significantly decreased hepcidin (WMD - 76.1 μg/L; 95% CI - 91.8 to - 60.3, p < 0.00001) and ferritin (WMD - 63.6 μg/L; 95% CI - 96.6 to - 30.7, p = 0.0002) compared with that of placebo groups. In addition, there was no significant difference in adverse events between the two groups. CONCLUSION:
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Authors | Dengpiao Xie, Jianting Wang, Xinping Wu, Mingquan Li |
Journal | International urology and nephrology
(Int Urol Nephrol)
Vol. 50
Issue 12
Pg. 2201-2206
(Dec 2018)
ISSN: 1573-2584 [Electronic] Netherlands |
PMID | 30073615
(Publication Type: Journal Article, Meta-Analysis, Review)
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Chemical References |
- Barbiturates
- GSK1278863
- Hemoglobins
- Hepcidins
- Prolyl-Hydroxylase Inhibitors
- Transferrin
- Hypoxia-Inducible Factor-Proline Dioxygenases
- Glycine
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Topics |
- Anemia
(blood, drug therapy, etiology)
- Barbiturates
(therapeutic use)
- Glycine
(analogs & derivatives, therapeutic use)
- Hemoglobins
(metabolism)
- Hepcidins
(blood)
- Humans
- Hypoxia-Inducible Factor-Proline Dioxygenases
(antagonists & inhibitors)
- Prolyl-Hydroxylase Inhibitors
(therapeutic use)
- Randomized Controlled Trials as Topic
- Renal Insufficiency, Chronic
(complications)
- Transferrin
(metabolism)
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