| CPC C12Q 1/6883 (2013.01) [C12Q 2600/112 (2013.01); C12Q 2600/158 (2013.01); C12Q 2600/178 (2013.01)] | 10 Claims |
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1. A method for treating a human patient with rapid progressing Parkinson's disease, comprising the steps of, in this order:
obtaining a first sample comprising serum, plasma or blood from said patient;
determining a level of expression of at least one miRNA selected from the group consisting of SEQ ID NOS: 33, 42 and 45, and optionally further determining a level of expression of at least one miRNA selected from the group consisting of SEQ ID NOS: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 34, 35, 36, 37, 38, 39, 40, 41, 43, 44, 46, 47, 48, 49, 50, 51 and 52 within said first sample;
comparing the level of expression of the determined SEQ ID NOS to a level of expression of the determined SEQ ID NOS in a second sample from a cohort with slow progressing Parkinson's disease and confirming the expression level of the determined SEQ ID NOS in said first sample is greater than 1.2-fold over that of said second sample, thereby indicating the patient has rapid progressing Parkinson's disease; and
treating said rapid progressing Parkinson's disease with at least one of L-dopa, a dopamine agonist, a catechol-O-methyltransferase (COMT) inhibitor, amantidine (1-Aminotricyclo (3,3,1,13,7) decane or a monoamino oxidase type B inhibitor.
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