Claims for Patent: 6,066,450

Summary for Patent: 6,066,450

Title:	Diagnostic and therapeutic methods and apparatus based on interleukin-6 gene polymorphisms
Abstract:	The present invention provides methods of diagnosis of certain disease states, such as osteoporosis, that are associated with polymorphisms in an IL-6 gene, comprising determining the genotype of an IL-6 gene. The invention is also directed to methods of identifying an individual predisposed or susceptible to certain disease states, such as osteoporosis, associated with polymorphisms of an IL-6 gene, comprising determining the genotype of an IL-6 gene in the affected individual. The invention is further directed to compositions useful for determining the genotype of an IL-6 gene, to kits and diagnostic apparatuses comprising such compositions, and to methods of treatment of diseases associated with IL-6 genetic polymorphisms.
Inventor(s):	Ralston; Stuart Hamilton (Aberdeen, GB), Grant; Struan Frederick Airth (Sydney, AU)
Assignee:	Gemini International Holdings Limited (MC)
Application Number:	08/857,464
Patent Claims:	1. A method of identifying an animal predisposed or susceptible to osteoporosis, said method comprising determining the presence of a C/F genotype or an F/F genotype in the 3' flanking region of an IL-6 gene in said animal, wherein said C/F genotype is correlated with decreased risk of osteoporosis and the F/F genotype is correlated with increased risk of osteoporosis, and wherein when said 3' flanking region of an IL-6 gene is amplified by PCR using nucleic acid primers having the nucleotide sequences as set forth in SEQ ID NO:1 and SEQ ID NO:2, said C/F genotype is indicated by obtaining DNA amplimers of sizes 695 bp and 675 bp and said F/F genotype is indicated by obtaining a DNA amplimer of size 675 bp. 2. The method of claim 1, wherein said animal is a human. 3. A method of treating an animal predisposed or susceptible to osteoporosis, said method comprising: (a) determining the presence of an F/F genotype in the 3' flanking region of an IL-6 gene in said animal wherein said F/F genotype is correlated with increased risk of osteoporosis, and wherein when said 3' flanking region of an IL-6 gene is amplified by PCR using nucleic acid primers having the nucleotide sequences as set forth in SEQ ID NO: 1 and SEQ ID NO:2, said F/F genotype is indicated by obtaining a DNA amplimer of size 675 bp; and (b) administering to said animal an effective dose of a therapeutic composition suitable to delay, reduce or prevent osteoporosis in said animal. 4. The method of claim 3, wherein said therapeutic composition comprises a compound selected from the group consisting of a hormone, a xanthine oxidase inhibitor, a substituted benzodiazepine, calcitonin, a bisphosphonate, sodium fluoride and calcitriol. 5. The method of claim 4, wherein said hormone is oestrogen, test testosterone on parathyroid hormone. 6. The method of claim 4, wherein said bisphosphonate is alendronate. 7. The method of claim 3, wherein said animal is human. 8. A method of determining or predisposition to osteoporosis in a human, said method comprising determining the presence of a C/F genotype or an F/F genotype in the 3' flanking region of an IL-6 gene in said human, wherein said C/F genotype is correlated with decreased risk of osteoporosis and the F/F genotype is correlated with increased risk of osteoporosis, and wherein when said 3' flanking region of an IL-6 gene is amplified by PCR using nucleic acid primers having nucleotide sequences as set forth in SEQ ID NO:1 and SEQ ID NO:2, said C/F genotype is indicated by obtaining DNA amplimers of sizes 695 bp and 675 bp and said F/F genotype is indicated by obtaining a DNA amplimer of size 675 bp. 9. A method of predicting an increased or decreased bone mineral density (BMD) in a human, said method comprising determining the presence of either a C/F or an F/F genotype in the 3' flanking region of an IL-6 gene in said human, wherein said C/F genotype is correlated with increased BMD and said F/F genotype is correlated with decreased BMD, and wherein when said 3' flanking region of an IL-6 gene is amplified by PCR using nucleic acid primers having nucleotide sequences as set forth in SEQ ID NO:1 and SEQ ID NO:2, said C/F genotype is indicated by obtaining DNA amplimers of sizes 695 bp and 675 bp and said F/F genotype is indicated by obtaining a DNA amplimer of size 675 bp. 10. A method of treating a human predisposed or susceptible to osteoporosis, said method comprising: a) determining the presence of either a C/F or an F/F genotype in the 3' flanking region of an IL-6 gene in a human, wherein said C/F genotype is correlated with decreased risk of osteoporosis and said F/F genotype is correlated with increased risk of osteoporosis and wherein when said 3' flanking region of an IL-6 gene is amplified by PCR using nucleic acid primers having nucleotide sequences as set forth in SEQ ID NO:1 and SEQ ID NO:2, a C/F genotype is indicated by obtaining DNA amplimers of sizes 695 bp and 675 bp and an F/F genotype is indicated by obtaining a DNA amplimer of size 675 bp; and b) administering to said human an effective dose of a therapeutic composition suitable to delay, reduce or prevent osteoporosis in said human. 11. The method of claim 3, wherein said therapeutic composition comprises a compound selected from the group consisting of a hormone, a xanthine oxidase inhibitor, a substituted benzodiazepine, calcitonin, a bisphosphonate, sodium fluoride and calcitriol. 12. The method of claim 4, wherein said hormone is oestrogen, testosterone or parathyroid hormone. 13. The method of claim 4, wherein said bisphosphonate is alendronate.

Details for Patent 6,066,450

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Nps Pharmaceuticals, Inc.	NATPARA	parathyroid hormone	For Injection	125511	01/23/2015		2016-05-16