| CPC A61K 31/53 (2013.01) [A61K 31/195 (2013.01); A61K 31/198 (2013.01); G01N 33/84 (2013.01); G01N 2800/2821 (2013.01)] | 3 Claims |

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1. A method of diagnosing and treating Alzheimer's disease and related dementias (ADRD) comprising:
obtaining a plasma sample from the patient;
determining a level of a biochemical sulfide in the plasma sample from the patient, the biochemical sulfide being one of acid-labile sulfide, bound sulfide, and total sulfide;
diagnosing the patient with ADRD when biochemical sulfide is above a cutoff; and administering an effective amount of a sulfide reducer to the diagnosed patient, wherein:
the sulfide reducer is a CSE inhibitor and includes one of L-propylarginine, L-aminoethoxyvinylglycine, I157172 (2-[(4-(2,5-dimethoxyanilino)-6-(3-nitroanilino)-1,3,5-triazin-2-yl) sulfanyl]-6-ethoxy-1,3-benzothiazole); or
the sulfide reducer is a CBS inhibitor and includes one of hydroxylamine, aminooxyacetic acid, trifluoroalanine, L-aminoethoxyvinylglycine, and both L-aminoethoxyvinylglycine and pyridoxamine; or
the sulfide reducer is an MST inhibitor and includes XMU-MP-1 (4-((5,10-dimethyl-6-oxo-6,10-dihydro-5H-pyrimido[5,4-b]thieno[3,2-e][1,4]diazepin-2-yl)amino)benzenesulfonamide).
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