Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease
The present invention provides a method of diagnosing a cerebrovascular disease in a human comprising the steps of: (a) measuring a mutation of HTRA1 gene in a test sample from said human; and (b) determining if the mutation of HTRA1 gene in said test sample correlates with a cerebrovascular disease in said human.
1. A method of determining the presence of a HTRA1 mutation in a human subject, comprising:
(a) obtaining a biological sample from a human subject;
(b) assaying a HTRA1 nucleic acid in the biological sample for a HTRA1 mutation selected from the group consisting of C>T at position 1108 of SEQ ID NO: 1, C>T at position 904 of SEQ ID NO: 1, G>A at position 889 of SEQ ID NO: 1, and G>A at position 754 of SEQ ID NO: 1 by contacting the HTRA1 nucleic acid with a detectably labeled oligonucleotide probe, wherein the detectably labeled oligonucleotide probe comprises a fragment of the complement of SEQ ID NO: 1, wherein the fragment includes an A at position 1108, an A at position 904, a T at position 889, or T at position 754 of SEQ ID NO: 1;
(c) detecting hybridization of the HTRA1 nucleic acid with the detectably labeled oligonucleotide probe; and
(d) determining the presence of the HTRA1 mutation comprising a C>T at position 1108 of SEQ ID NO: 1, C>T at position 904 of SEQ ID NO: 1, G>A at position 889 of SEQ ID NO: 1, or G>A at position 754 of SEQ ID NO: 1.
2. The method according to claim 1 , wherein the HTRA1 nucleic acid is present in or derived from the biological sample selected from the group consisting of blood, serum, plasma, saliva, cerebral spinal fluid, oral mucosa and nail.
3. The method according to claim 1 , wherein the biological sample is blood.
4. The method of claim 1 , wherein the mutation is C904T.