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Optimal range: 4 - 52 mmol/mol creatinine
Alpha-Ketoglutarate is an organic acid that is important for the proper metabolism of all essential amino acids. It is formed in the Krebs cycle, the energy-producing process that occurs in most body cells.
Optimal range: 0 - 169.6 nmol/mg Creatinine
Alpha-Ketoglutarate is an organic acid that is important for the proper metabolism of all essential amino acids. It is formed in the Krebs cycle, the energy-producing process that occurs in most body cells.
Optimal range: 4 - 52 mmol/mol creatinine
Isocitric Acid is converted to α-ketoglutaric acid using the enzyme isocitrate dehydrogenase. Alphaketoglutarate is a rate-determining intermediate in the Citric Acid Cycle and provides an important source of glutamine and glutamate that stimulates protein synthesis and bone tissue formation, inhibits protein degradation in muscle, and constitutes an important metabolic fuel for cells of the gastrointestinal tract. Alpha-ketoglutaric acid is then converted to Succinyl CoA using the enzyme alpha-ketoglutarate dehydrogenase. This enzyme complex is very similar to the pyruvate dehydrogenase complex with similar nutrient cofactor needs.
Optimal range: 0 - 21.72 ug/mgCR
Isocitric Acid is converted to α-ketoglutaric acid using the enzyme isocitrate dehydrogenase. Alphaketoglutarate is a rate-determining intermediate in the Citric Acid Cycle and provides an important source of glutamine and glutamate that stimulates protein synthesis and bone tissue formation, inhibits protein degradation in muscle, and constitutes an important metabolic fuel for cells of the gastrointestinal tract. Alpha-ketoglutaric acid is then converted to Succinyl CoA using the enzyme alpha-ketoglutarate dehydrogenase. This enzyme complex is very similar to the pyruvate dehydrogenase complex with similar nutrient cofactor needs.
Optimal range: 4 - 52 mmol/mol creatinine
Alpha-Ketoglutarate is an organic acid that is important for the proper metabolism of all essential amino acids. It is formed in the Krebs cycle, the energy-producing process that occurs in most body cells.
Optimal range: 0 - 0.89 mmol/mol creatinine
Alpha-Ketoisocaproate is a B-Complex Vitamin Marker (Leucine catabolism).
Optimal range: 0 - 20.4 nmol/mg Creatinine
2-Ketoisocaproic Acid is a B-Complex Vitamin Marker (Leucine catabolism).
2-Ketoisocaproic Acid is an abnormal metabolite that arises from the incomplete breakdown of branched-chain amino acids.
Optimal range: 0 - 0.89 mmol/mol creatinine
Of the essential amino acids, there are three branchedchain amino acids (leucine, isoleucine, and valine).
Unlike most amino acids, the initial step of branchedchain amino acid (BCAA) metabolism does not take place in the liver. They increase rapidly in systemic circulation after protein intake and are readily available for use. Skeletal muscle is where most of the initial catabolism of BCAA takes place using branched-chain aminotransferase enzymes to form α-ketoacids, which are then released from muscles back into the blood to be further metabolized, mainly in the liver.
BCAA act as substrates for protein synthesis, energy production, neurotransmitter production, glucose metabolism, immune response, and many other beneficial metabolic processes.
α-Ketoisovaleric Acid (AKIV) is produced from the essential amino acid valine. It then metabolizes to become succinyl Co-A. AKIV is glucogenic.
α-Ketoisocaproic Acid (AKIC) is produced from leucine and further metabolizes to form acetyl-CoA and acetoacetate. AKIC is ketogenic.
α-Keto-β-Methylvaleric Acid (AKBM) comes from isoleucine, and further metabolizes to form acetylCoA and succinyl-CoA. AKBM is therefore both glycogenic and ketogenic.
These α-ketoacids then require an enzyme complex called branched-chain α-keto acid dehydrogenase (BCKD) for further metabolism.
This enzyme complex requires multiple vitamin cofactors, such as vitamin B1, B2, B3, B5, and lipoic acid.
Optimal range: 0 - 0.89 mmol/mol creatinine
a-Ketoisocaproic Acid is a B-Complex Vitamin Marker (Leucine catabolism).
Optimal range: 0 - 0.34 ug/mgCR
Of the essential amino acids, there are three branchedchain amino acids (leucine, isoleucine, and valine).
Unlike most amino acids, the initial step of branchedchain amino acid (BCAA) metabolism does not take place in the liver. They increase rapidly in systemic circulation after protein intake and are readily available for use. Skeletal muscle is where most of the initial catabolism of BCAA takes place using branched-chain aminotransferase enzymes to form α-ketoacids, which are then released from muscles back into the blood to be further metabolized, mainly in the liver.
BCAA act as substrates for protein synthesis, energy production, neurotransmitter production, glucose metabolism, immune response, and many other beneficial metabolic processes.
α-Ketoisovaleric Acid (AKIV) is produced from the essential amino acid valine. It then metabolizes to become succinyl Co-A. AKIV is glucogenic.
α-Ketoisocaproic Acid (AKIC) is produced from leucine and further metabolizes to form acetyl-CoA and acetoacetate. AKIC is ketogenic.
α-Keto-β-Methylvaleric Acid (AKBM) comes from isoleucine, and further metabolizes to form acetylCoA and succinyl-CoA. AKBM is therefore both glycogenic and ketogenic.
These α-ketoacids then require an enzyme complex called branched-chain α-keto acid dehydrogenase (BCKD) for further metabolism.
This enzyme complex requires multiple vitamin cofactors, such as vitamin B1, B2, B3, B5, and lipoic acid.
Optimal range: 0 - 0.97 mmol/mol creatinine
Alpha-Ketoisovalerate (together with Alpha-Ketoisocaproate and Alpha-Keto-Beta-methylvalerate) requires Vitamins B1, B2, B3, B5 and lipoic acid to be metabolized.
Optimal range: 0 - 6.1 nmol/mg Creatinine
Alpha-Ketoisovalerate (together with Alpha-Ketoisocaproate and Alpha-Keto-Beta-methylvalerate) requires Vitamins B1, B2, B3, B5 and lipoic acid to be metabolized.
Optimal range: 0 - 0.97 mmol/mol creatinine
Of the essential amino acids, there are three branchedchain amino acids (leucine, isoleucine, and valine).
Unlike most amino acids, the initial step of branchedchain amino acid (BCAA) metabolism does not take place in the liver. They increase rapidly in systemic circulation after protein intake and are readily available for use. Skeletal muscle is where most of the initial catabolism of BCAA takes place using branched-chain aminotransferase enzymes to form α-ketoacids, which are then released from muscles back into the blood to be further metabolized, mainly in the liver.
BCAA act as substrates for protein synthesis, energy production, neurotransmitter production, glucose metabolism, immune response, and many other beneficial metabolic processes.
α-Ketoisovaleric Acid (AKIV) is produced from the essential amino acid valine. It then metabolizes to become succinyl Co-A. AKIV is glucogenic.
α-Ketoisocaproic Acid (AKIC) is produced from leucine and further metabolizes to form acetyl-CoA and acetoacetate. AKIC is ketogenic.
α-Keto-β-Methylvaleric Acid (AKBM) comes from isoleucine, and further metabolizes to form acetylCoA and succinyl-CoA. AKBM is therefore both glycogenic and ketogenic.
These α-ketoacids then require an enzyme complex called branched-chain α-keto acid dehydrogenase (BCKD) for further metabolism.
This enzyme complex requires multiple vitamin cofactors, such as vitamin B1, B2, B3, B5, and lipoic acid.
Optimal range: 0 - 1.15 ug/mgCR
Of the essential amino acids, there are three branchedchain amino acids (leucine, isoleucine, and valine).
Unlike most amino acids, the initial step of branchedchain amino acid (BCAA) metabolism does not take place in the liver. They increase rapidly in systemic circulation after protein intake and are readily available for use. Skeletal muscle is where most of the initial catabolism of BCAA takes place using branched-chain aminotransferase enzymes to form α-ketoacids, which are then released from muscles back into the blood to be further metabolized, mainly in the liver.
BCAA act as substrates for protein synthesis, energy production, neurotransmitter production, glucose metabolism, immune response, and many other beneficial metabolic processes.
α-Ketoisovaleric Acid (AKIV) is produced from the essential amino acid valine. It then metabolizes to become succinyl Co-A. AKIV is glucogenic.
α-Ketoisocaproic Acid (AKIC) is produced from leucine and further metabolizes to form acetyl-CoA and acetoacetate. AKIC is ketogenic.
α-Keto-β-Methylvaleric Acid (AKBM) comes from isoleucine, and further metabolizes to form acetylCoA and succinyl-CoA. AKBM is therefore both glycogenic and ketogenic.
These α-ketoacids then require an enzyme complex called branched-chain α-keto acid dehydrogenase (BCKD) for further metabolism.
This enzyme complex requires multiple vitamin cofactors, such as vitamin B1, B2, B3, B5, and lipoic acid.
Optimal range: 0 - 0.97 mmol/mol creatinine
Alpha-Ketoisovalerate (together with Alpha-Ketoisocaproate and Alpha-Keto-Beta-methylvalerate) requires Vitamins B1, B2, B3, B5 and lipoic acid to be metabolized.
Optimal range: 0 - 0.46 mmol/mol creatinine
α-Ketophenylacetic Acid, also known as phenylglyoxylic acid (PGA), is a urinary metabolite of styrene, toluene, xylenes, and ethylbenzene.
It acts as a urinary marker of recent exposure via inhalation, contact, oral, and others.
The biologic half-life of styrene in humans is fairly short and corresponds with the disappearance of PGA from the urine. Styrene is widely used for synthesis of polymers such as plastics, rubbers, and surface coating. It is also used in the pharmaceutical industry. Styrene is commonly applied in the manufacturing of paints, pigments, and glues. Coexposure to other solvents, like toluene and ethyl acetate is common in workplaces where styrene is a concern. Since toluene and xylene are components of unleaded gasoline, workers at gas stations are at potential risk of exposure, as well as the general population.
Styrene exposure may interfere with peripheral metabolism of thyroid hormones by inhibiting conversion of T4 to T3.
It may also affect DNA repair capacity and damage. There are also clinical associations with insulin resistance, oxidative stress, and inflammation.
Optimal range: 0 - 0.46 mmol/mol creatinine
a-Ketophenylacetic Acid (from Styrene) is a toxic breakdown product.
Optimal range: 0 - 0.46 mmol/mol creatinine
α-Ketophenylacetic Acid, also known as phenylglyoxylic acid (PGA), is a urinary metabolite of styrene, toluene, xylenes, and ethylbenzene.
It acts as a urinary marker of recent exposure via inhalation, contact, oral, and others.
The biologic half-life of styrene in humans is fairly short and corresponds with the disappearance of PGA from the urine. Styrene is widely used for synthesis of polymers such as plastics, rubbers, and surface coating. It is also used in the pharmaceutical industry. Styrene is commonly applied in the manufacturing of paints, pigments, and glues. Coexposure to other solvents, like toluene and ethyl acetate is common in workplaces where styrene is a concern. Since toluene and xylene are components of unleaded gasoline, workers at gas stations are at potential risk of exposure, as well as the general population.
Styrene exposure may interfere with peripheral metabolism of thyroid hormones by inhibiting conversion of T4 to T3.
It may also affect DNA repair capacity and damage. There are also clinical associations with insulin resistance, oxidative stress, and inflammation.
Optimal range: 0.09 - 1 wt %
Alpha-linolenic acid (ALA) is plant-based essential omega-3 polyunsaturated fatty acids that must be obtained through the diet.
Optimal range: 0.28 - 5 wt %
Alpha-linolenic acid (ALA) is an essential n-3 fatty acid and must be obtained in the diet. Sources include green leafy vegetables, oily fish, flaxseed, soybean oil, canola oil, walnuts, and chia seeds. ALA has an 18-carbon backbone with 3 double bonds starting at the third carbon molecule (18:3n3). It is an important precursor to make eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), though these can also be obtained in the diet. Most dietary ALA is used to generate energy and only a small portion is converted to EPA and DHA.