COVALENTLY BOUND METABOLITES AS BIOMARKERS
A method for determining the systems biology state of an animal, which comprises determining levels of small molecules covalently bound to macromolecules (CBSM) in samples from that animal, and using said levels to determine the risk, diagnostic state and progression of disease in that animal. A therapy development method for determining the structure of covalently bound molecules and their precursors and modifying the sources and mechanisms causing such binding to reduce disease risk and progression.
1 . A method for determining a disease state of an animal, which comprises determining levels of small molecules covalently bound to macromolecules (CBSM) in samples from that animal, and comparing said levels to standards.
2 . The method of claim 1 , wherein the CBSM small molecules are sourced from gut microbiome derived, derived from metabolic processes, environmental chemical insult or abnormal chemical environment, endogenous or exogenous microorganism, or an interaction of processes between one or more of the above sources.
3 . The method of claim 1 , wherein the macromolecule is selected from the group
consisting of DNA, RNA, Protein, a complex carbohydrate and a Glycoprotein.
4 . The method of claim 1 , wherein the disease state is selected from the group consisting of disease classification, disease sub categorization, disease progression, development of risk factors predictive of disease, specification of therapy, prediction of therapeutic outcome and development of therapeutic leads.
5 . The method of claim 1 , wherein the animal is a human.
6 . A method for therapeutic intervention in disease in an animal comprising manipulating concentration levels of small molecules covalently bound to macromolecules (CBSM).
7 . The method of claim 6 , wherein the macromolecule is selected from the group
consisting of DNA, RNA, Protein, a complex carbohydrate and a Glycoprotein.
8 . The method of claim 6 , wherein the small molecules are sourced from gut microbiome derived, derived from metabolic processes, environmental chemical insult or abnormal chemical environment, endogenous or exogenous microorganism, or an interaction of processes between and among one or more the above sources.
9 . The method of claim 6 , wherein the disease is an affective disease selected from the group consisting of depression, schizophrenia and autism, a degenerative disease selected from the groups consisting of Huntington's, Alzheimer's, Parkinson's, Mild Cognitive impairment, ALS, Freidrich Ataxia, cancer, diabetes, and cardiovascular disease, or from in-born errors of metabolism or genetic based disease.
10 . The method of claim 6 , wherein the animal is a human.
11 . A method of intervention to prevent or ameliorate disease in an animal with disease risk which comprises manipulating the animal's small molecules covalently bound to macromolecules (CBSM).
12 . The method of claim 11 , wherein the risk is for an affective disease selected from the group consisting of depression, schizophrenia and autism, a degenerative disease selected from the group consisting of Huntington's, Alzheimer's, Parkinson's, Mild Cognitive impairment, ALS or Freidrich Ataxia, cancer, diabetes, and cardiovascular disease or from in-born errors of metabolism or genetic based disease.
13 . The method of claim 11 , wherein the animal is a human.
14 . A method for determining the nature of the source of small molecules covalently bound to macromolecules (CBSM) which comprises creating and analyzing synthetic combinations of small molecules and macromolecules with processes mimicking biochemical processes in an animal.
15 . The method of claim 14 , wherein the animal comprises a human.
16 . A method for modifying gene function in an animal comprising manipulating concentration levels of small molecules covalently hound to macromolecules (CBSM), whereby to increase or decrease expression of a target gene.
17 . The method of claim 16 , wherein the macromolecule is selected from the group consisting of DNA, RNA, a Protein, a complex carbohydrate and a Glycoprotein.
18 . The method of claim 16 , wherein the small molecule is sourced from gut microbiome derived, derived from metabolic processes, environmental chemical insult or abnormal chemical environment, endogenous or exogenous microorganism, or an interaction of processes between and among one or more the above sources.
19 . The method of claim 16 , wherein the gene is associated with an affective disease selected from the group consisting of depression, schizophrenia or autism, a degenerative disease selected from the group consisting of Huntington's, Alzheimer's, Parkinson's, Mild Cognitive impairment, ALS, Freidrich Ataxia, cancer, diabetes, cardiovascular, or from in-born errors of metabolism or genetic based.
20 . The method of claim 16 , wherein the animal is a human.
21 . A method of therapeutic discovery comprising:
identifying a class of subjects with equivalent genetic risk factors;
identifying sub classes in this class who do and do not develop disease;
identifying differences in covalently bound molecules to DNA, RNA and protein that discriminate the class and subclasses and affect epigenetic differences in the system feedback control;
isolating and determining chemical precursor sources and structures of the covalently bound discriminators; and
providing or replacing such compounds as are missing or in reduced amount in the disease developing class and/or suppressing such compounds that are elevated or in excess in the disease developing class.
22 . The method of discovery in 21 wherein the disease is a neurodegenerative disease selected from the group consisting of Huntington's, Parkinson's, Mild Cognitive Impairment, Amyotrophic Lateral Sclerosis, Freidrich Ataxia, cancer, diabetes and cardiovascular disease, an affective disorder selected from the group consisting of depression, schizophrenia and autism, or from in-born errors of metabolism or genetic based disease.
23 . Small molecules covalently bound to macromolecules for determination of disease risk, diagnostic status, prediction of progression and development of therapy.