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口服磷酸盐结合剂:历史与展望。

Oral phosphate binders: history and prospects.

机构信息

Division of Nephrology and Intensive Care Medicine, Niigata University Medical and Dental Hospital, Niigata, 951-8510, Japan.

出版信息

Bone. 2009 Jul;45 Suppl 1:S8-12. doi: 10.1016/j.bone.2009.01.005. Epub 2009 Jan 20.

Abstract

The use of an oral phosphate binder is a promising and most practical strategy for the prevention of vascular calcification in patients with chronic kidney disease (CKD). To secure the safety: 1) the oral phosphate binder must not cause adverse effects in the gastrointestinal tract; 2) the oral phosphate binder should be non-absorbable or barely absorbable through the gastrointestinal tract, or 3) if partially absorbed through the gastrointestinal tract, it must be eliminated from circulation through a pathway other than urinary excretion, and 4) even if it accumulates in the body, it should not cause organ dysfunctions. Metal salt type oral phosphate binder is the most classical type of oral phosphate binders that includes aluminum hydroxide gel and lanthanum carbonate. These oral phosphate binders effectively adsorb phosphate ions, however, have a potential risk for accumulation and intoxication. Calcium salt type oral phosphate binder was the most widely prescribed oral phosphate binder in the last decade but is now believed to exert potential harm, favoring progression of vascular calcification through excessive intestinal calcium load. However, recent studies failed to detect an inferiority of calcium salt type oral phosphate binders as compared to non-calcium salt type oral phosphate binders in terms of mortality and/or morbidity of hemodialysis patients. Polymerized resin type is a safe and relatively effective oral phosphate binder, which is supported by many clinical evidences. However, it sometimes causes severe constipation, especially in Japanese patients. Among metal compound type oral phosphate binder, other promising compounds include boehmite-type aluminum and hydrotalcite-like compounds but they are not yet available in the clinical setting.

摘要

口服磷酸盐结合剂的使用是预防慢性肾脏病(CKD)患者血管钙化的一种有前途且最实用的策略。为确保安全性:1)口服磷酸盐结合剂不得在胃肠道引起不良反应;2)口服磷酸盐结合剂应通过胃肠道不可吸收或几乎不被吸收,或者 3)如果通过胃肠道部分吸收,则必须通过除尿液排泄以外的途径从循环中消除,并且 4)即使在体内积累,也不应引起器官功能障碍。

金属盐型口服磷酸盐结合剂是最经典的口服磷酸盐结合剂,包括氢氧化铝凝胶和碳酸镧。这些口服磷酸盐结合剂可有效吸附磷酸根离子,但存在潜在的蓄积和中毒风险。

钙盐型口服磷酸盐结合剂是过去十年中最广泛使用的口服磷酸盐结合剂,但现在认为它通过肠道钙负荷过多而对血管钙化的进展有潜在危害。然而,最近的研究未能检测到钙盐型口服磷酸盐结合剂与非钙盐型口服磷酸盐结合剂在血液透析患者的死亡率和/或发病率方面存在劣势。

聚合树脂型是一种安全且相对有效的口服磷酸盐结合剂,得到了许多临床证据的支持。然而,它有时会引起严重的便秘,尤其是在日本患者中。

在金属化合物型口服磷酸盐结合剂中,其他有前途的化合物包括勃姆石型铝和类水滑石化合物,但它们尚未在临床环境中使用。

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