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Method of Safely and Effectively Treating and Preventing Secondary Hyperparathyroidism in Chronic Kidney Disease

a hyperparathyroidism and kidney disease technology, applied in the field of safe and effective treatment and preventing secondary hyperparathyroidism in chronic kidney disease, can solve the problems of inability to sustain normal blood levels of 1,25-dihydroxyvitamin d in advanced ckd, little evidence of feedback regulation of extrahepatic prohormone production, and secondary hyperparathyroidism can also develop, so as to prevent the recurrence of secondary hyperparathyroidism, effective and safe use 25

Inactive Publication Date: 2010-06-10
OPKO RENAL LLC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0027]Given this invention, which is described in more detail herein, it becomes possible, for the first time, to (1) effectively and safely use 25-hydroxyvitamin D3 with or without 25-hydroxyvitamin D2, and/or Vitamin D3 with or without Vitamin D2, to treat secondary hyperparathyroidism due to Vitamin D insufficiency or deficiency in the early stages of CKD; (2) concurrently apply these Vitamin D repletion therapies and Vitamin...

Problems solved by technology

Secondary hyperparathyroidism can also develop in individuals with healthy kidneys, due to environmental, cultural or dietary factors which prevent adequate Vitamin D supply.
However, there is little evidence of feedback regulation of extrahepatic prohormone production.
Vitamin D prohormones can be metabolized into hormones outside of the kidneys in keratinocytes, lung epithelial cells, enterocytes, cells of the immune system (e.g., macrophages) and certain other cells containing CYP27B1 or similar enzymes, but such extrarenal hormone production is incapable of sustaining normal blood levels of 1,25-dihydroxyvitamin D in advanced CKD.
Oversuppression of PTH secretion can cause or exacerbate disturbances in calcium homeostasis and has been linked to vascular calcification.
Without early detection and treatment, followed by consistent maintenance or preventative therapy, secondary hyperparathyroidism progressively increases in severity, causing debilitating metabolic bone diseases, including osteoporosis and renal osteodystrophy.
Chronically low blood levels of 1,25-dihydroxyvitamin also develop because of a deficiency of Vitamin D prohormones, since renal hormone production cannot proceed without the required precursors.
Unfortunately, early detection and treatment of secondary hyperparathyroidism in CKD is rare, let alone prevention.
However, they cannot be administered in high enough doses to control elevated iPTH in all patients and they sporadically cause side effects, including hypercalcemia, hyperphosphatemia, hyercalciuria and oversuppression of iPTH, in a significant minority of the patients.
Health care professionals are cautious in raising the dose of these hormone replacement therapies for purposes of improving the control of secondary hyperparathyroidism in patients with excessive iPTH levels due to the increasing risk of causing such side effects.
As explained above, all CKD patients eventually develop decreased levels of renal CYP27B1 as kidney insufficiency becomes more severe, making it even more difficult, and eventually impossible, to treat secondary hyperparathyroidism with Vitamin D repletion therapies alone.

Method used

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Examples

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example 1

Efficacy Study in Patients With Stage 4 CKD and Secondary Hyperparathyroidism Associated With Vitamin D Insufficiency

[0061]The effectiveness of 25-hydroxyvitamin D3 and, as necessary, 1,25-dihydroxyvitamin D2 in restoring serum total 25-hydroxyvitamin D to optimal levels (>30 ng / mL) and serum total 1,25-dihydroxyvitamin D to adequate levels (>25 pg / mL) is examined in an open-ended study of adult male and female patients with Stage 4 CKD and secondary hyperparathyroidism associated with vitamin D insufficiency. Two formulations are used in the study. One of the formulations (Formulation #1) is a soft gelatin capsule containing 30 μg of 25-hydroxyvitamin D3. The second formulation (Formulation #2) is a soft gelatin capsule containing 0.25 μg of 1,25-dihydroxyvitamin D2.

[0062]A total of 100 subjects participate in this study, all of whom are aged 30 to 70 years and have serum 25-hydoxyvitamin D levels between 15 and 29 ng / mL (inclusive) and serum intact parathyroid hormone (iPTH) level...

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Abstract

A method of treating and preventing secondary hyperparathyroidism in CKD by increasing or maintaining blood concentrations of both 25-hydroxyvitamin D and 1,25-dihydroxyvitamin Din a patient by administering 25-hydroxyvitamin D3 with or without 25-hydroxyvitamin D2 and, as necessary, 1,25-dihydroxyvitamin D2 as a Vitamin D hormone replacement therapy.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]The benefit under 35 U.S.C. §119(e) of U.S. Provisional Patent Application Ser. No. 60 / 913,850 filed Apr. 25, 2007, is hereby claimed.BACKGROUND[0002]Secondary hyperparathyroidism is a disorder which develops primarily because of Vitamin D deficiency. It is characterized by abnormally elevated blood levels of parathyroid hormone (PTH) and, in the absence of early detection and treatment, it becomes associated with parathyroid gland hyperplasia and a constellation of metabolic bone diseases. It is a common complication of chronic kidney disease (CKD), with rising incidence as CKD progresses. Secondary hyperparathyroidism can also develop in individuals with healthy kidneys, due to environmental, cultural or dietary factors which prevent adequate Vitamin D supply.[0003]“Vitamin D” is a term that refers broadly to the organic substances named[0004]Vitamin D2, Vitamin D3, Vitamin D4, etc., and to their metabolites and hormonal forms that influ...

Claims

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Application Information

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IPC IPC(8): A61K31/593A61K31/592A61P5/20A61P5/18A61P13/12
CPCA61K31/59A61K31/593A61K31/592A61K2300/00A61K45/06A61P13/12A61P3/02A61P43/00A61P5/16A61P5/18A61P5/20
Inventor BISHOP, CHARLES W.
Owner OPKO RENAL LLC
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