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Maintenance of elevated fetal hemoglobin levels by decitabine during dose interval treatment of sickle cell anemia.
Author: BresslerLinda, DeSimoneJoseph, DornLouise, KoshyMabel, LavelleDonald, MolokieRobert, TalischyNasrin
Original Abstract of the Article :
We have previously demonstrated that 5-aza-2'-deoxycytidine (decitabine) augments fetal hemoglobin (HbF) levels in patients with sickle cell anemia (SS) who did not respond to hydroxyurea (HU). The present study was designed to determine the effect of repeated decitabine dosing on HbF levels and hem...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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引用元:
https://pubmed.ncbi.nlm.nih.gov/12010787
データ提供:米国国立医学図書館(NLM)
Decitabine: A Promising Treatment for Sickle Cell Anemia
Sickle cell anemia is a serious genetic blood disorder that affects red blood cells, leading to chronic pain, fatigue, and other complications. While hydroxyurea (HU) is currently the standard treatment, not all patients respond to it, prompting the search for alternative therapies. This study explored the potential of decitabine, a drug known to increase fetal hemoglobin (HbF) levels, as a treatment option for sickle cell anemia patients who don't respond to HU.
A New Hope for Sickle Cell Anemia Patients
The researchers administered decitabine to seven patients with sickle cell anemia, including five who had not responded to HU. They found that repeated decitabine dosing effectively increased HbF levels without causing significant side effects or toxicity. The average HbF levels increased from 3.12% to 13.93% during the 9-month treatment period. The study also noted an increase in hemoglobin (Hb) levels, indicating improved overall blood health.
Improving Quality of Life for Sickle Cell Anemia Patients
This research highlights the potential of decitabine as a viable treatment option for patients with sickle cell anemia who don't respond to HU. By increasing HbF levels, decitabine may help alleviate some of the symptoms and complications associated with this disease, improving patients' quality of life. However, further research is needed to determine the long-term effects of decitabine treatment and to refine the optimal dosing regimen.
Dr. Camel's Conclusion
The findings of this study are like a refreshing oasis in the desert for sickle cell anemia patients. Decitabine offers a potential solution for those who don't respond to current treatments, providing hope for a better future. Like a determined camel traversing a vast expanse, researchers are continuing to explore new avenues for treating sickle cell anemia, seeking to bring relief and improve the lives of those affected by this challenging disease.
Date :
- Date Completed 2002-07-01
- Date Revised 2021-02-16
Further Info :
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