Raloxifene in Hemodialysis Patients

AUTHORS

Frieder Keller 1 , *

1 Nephrology Department, University Hospital, Ulm, Germany

How to Cite: Keller F. Raloxifene in Hemodialysis Patients, Int J Endocrinol Metab. 2012 ; 10(3):576-576. doi: 10.5812/ijem.5457.

ARTICLE INFORMATION

International Journal of Endocrinology and Metabolism: 10 (3); 576-576
Published Online: June 30, 2012
Article Type: Letter
Received: May 6, 2012
Revised: May 7, 2012
Accepted: May 7, 2012
Crossmark

Crossmark

CHEKING

READ FULL TEXT

Keywords

Raloxifene Oxidative Stress

Copyright © 2012, Research Institute For Endocrine Sciences and Iran Endocrine Society. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

Dear Editor,

There is good news for the renal patients since more treatment options have been derived for Chronic Kidney Disease-Mineral Bone Disorder (CKD-MBD) apart from suppressing parathyroid hormone levels. The role of parathyroid hormone apparently seems to be clear. However, it is still unclear what ‘adynamic bone’ disease really means.

Whether renal patients treated with supra-physiological parathyroid hormone would not suffer from adynamic bone disease? Or ‘adynamic bone disease’ is a specific form of osteoporosis in renal patients?

The beneficial effect of raloxifene, an established osteoporosis treatment now has been shown on bone mineral density in both, diabetic and non-diabetic dialysis patients (1). Bone resorption was less, parathyroid hormone levels decreased and bone density was improved by raloxifene. Bone mineral density also improved while on raloxifene treatment in postmenopausal women with CKD before dialysis (2). Thus, ‘adynamic bone disease’ the presumed osteoporosis subtype of CKD-MBD could be seen as the metabolic consequence of sex hormone deficits. The next step might be a raloxifene trial even in men with CKD. At present it will be prudent, however, to use the lower dose of 60 mg per day since raloxifene exposure is higher in renal patients (3). In addition, such treatment should be restricted to 1 year because safety and cardiovascular risks after long-term use are still unknown in this population.

Footnotes

References

  • 1.

    Saito O, Saito T, Asakura S, Akimoto T, Inoue M, Ando S, et al. Effects of raloxifene on bone metabolism in hemodialysis patients with type 2 diabetes. Int J Endocrinol Metab. 2012; 10 : 464 -9 [DOI]

  • 2.

    Czock D, Keller F, Heringa M, Rasche FM. Raloxifene pharmacokinetics in males with normal and impaired renal function. Br J Clin Pharmacol. 2005; 59(4) : 479 -82 [DOI][PubMed]

  • 3.

    Ishani A, Blackwell T, Jamal SA, Cummings SR, Ensrud KE. The effect of raloxifene treatment in postmenopausal women with CKD. J Am Soc Nephrol. 2008; 19(7) : 1430 -8 [DOI][PubMed]

  • COMMENTS

    LEAVE A COMMENT HERE: