🍽️ clofibric acid non-drug

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  1. Hypolipidemic Effects: Clofibric acid belongs to a class of drugs known as fibric acid derivatives, which are primarily used to lower lipid levels in the blood. These drugs work by activating peroxisome proliferator-activated receptor alpha (PPAR-Ξ±), leading to increased lipolysis and decreased synthesis of triglycerides. However, clofibric acid itself is not widely used for this purpose due to its relatively weak lipid-lowering effects compared to other fibric acid derivatives like gemfibrozil and fenofibrate.

  2. Anti-inflammatory Properties: Clofibric acid has been shown to exhibit anti-inflammatory effects, possibly through its modulation of PPAR-Ξ± activity. Some studies suggest that it may have potential therapeutic applications in inflammatory conditions, although further research is needed to elucidate its mechanisms of action and efficacy.

  3. Metabolism and Excretion: Clofibric acid is primarily metabolized in the liver and excreted in the urine. It undergoes conjugation with glycine to form clofibryl glycine, which is then excreted. The pharmacokinetics of clofibric acid have been studied in relation to its lipid-lowering effects and potential adverse effects.

  4. Adverse Effects: While clofibric acid has been associated with beneficial effects on lipid metabolism and inflammation in some studies, it may also be associated with certain adverse effects. These may include gastrointestinal disturbances, liver toxicity, and muscle-related adverse effects such as myopathy or rhabdomyolysis. However, because clofibric acid is not commonly used clinically, the prevalence and severity of adverse effects associated with its use are not well-characterized.

  5. Drug Interactions: Clofibric acid may interact with other medications, particularly those metabolized by the cytochrome P450 system or those that affect lipid metabolism. Healthcare providers should be aware of potential drug interactions when prescribing or considering the use of clofibric acid.

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Data Contradictions β€” Limits of Certainity

Impacted of clofibric acid non-drug On Probiotics

Rank Probiotic Impact
genus Bifidobacterium Reduces
species Akkermansia muciniphila Reduces
species Bacteroides uniformis Reduces
species Bifidobacterium longum Reduces
species Lacticaseibacillus paracasei Reduces
subspecies Bifidobacterium longum subsp. infantis Reduces
subspecies Bifidobacterium longum subsp. longum Reduces

Bacteria Impacted by clofibric acid non-drug

We extend modifiers to include items that changes the parent and child taxa. I.e. for a species, that would be the genus that is belongs to and the strains in the species.

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Taxonomy Rank Effect Citations Notation
Akkermansiaceae family Decreases 👪 Source Study
Dorea genus Decreases 👪 Source Study
Roseburia genus Decreases 👪 Source Study
Bacteroides genus Decreases 👪 Source Study
Bifidobacterium genus Decreases 👪 Source Study
Bilophila genus Decreases 👪 Source Study High Level Cause Brain Fog(Cognitive impairment)
Clostridioides genus Decreases 👪 Source Study
Lachnospira genus Decreases 👪 Source Study
Lacrimispora genus Decreases 👪 Source Study
Mediterraneibacter genus Decreases 👪 Source Study
Streptococcus genus Decreases 👪 Source Study
Akkermansia genus Decreases 📓 Source Study
Lacticaseibacillus genus Decreases 👪 Source Study
environmental samples no rank Decreases 👶 Source Study
unclassified Akkermansia no rank Decreases 👶 Source Study
Lacticaseibacillus paracasei species Decreases 📓 Source Study
Lachnospira eligens species Decreases 📓 Source Study
Lacrimispora saccharolytica species Decreases 📓 Source Study
Bilophila wadsworthia species Decreases 📓 Source Study
Akkermansia massiliensis species Decreases 👶 Source Study
Candidatus Akkermansia intestinavium species Decreases 👶 Source Study
Akkermansia muciniphila species Decreases 📓 Source Study High Levels linked to long-lived individuals
Bacteroides uniformis species Decreases 📓 Source Study Infectious bacteria
Dorea formicigenerans species Decreases 📓 Source Study
Bacteroides fragilis species Decreases 📓 Source Study H02076 Bacteroides infection
Clostridioides difficile species Decreases 📓 Source Study Colitis
Mediterraneibacter gnavus species Decreases 📓 Source Study
Bifidobacterium longum species Decreases 📓 Source Study
Roseburia hominis species Decreases 📓 Source Study
Akkermansia glycaniphila species Decreases 👶 Source Study
Streptococcus salivarius species Decreases 📓 Source Study Infectious bacteria
Bifidobacterium longum subsp. longum subspecies Decreases 👶 Source Study
Bifidobacterium longum subsp. infantis subspecies Decreases 👶 Source Study
Bifidobacterium longum subsp. suis subspecies Decreases 👶 Source Study
Lacticaseibacillus paracasei subsp. paracasei subspecies Decreases 👶 Source Study
Lacticaseibacillus paracasei subsp. tolerans subspecies Decreases 👶 Source Study
Bifidobacterium longum subsp. suillum subspecies Decreases 👶 Source Study

Impact of clofibric acid non-drug on Conditions from US National Library of Medicine

A higher number indicates impact on more bacteria associated with the condition and confidence on the impact.

We have X bacteria high and Y low reported. We find that the modifier reduces some and increases other of these two groups. We just tally: X|reduces + Y|Increase = Positive   X|increases + Y|decrease = Negative.

Benefit Ratio:
Numbers above 0 have increasing positive effect.
Numbers below 0 have increasing negative effect.

Condition Positive Impact Negative Impact Benefit Ratio Impact
Abdominal Aortic Aneurysm 0.3 0.3
Acne 0.3 -0.3
ADHD 1.3 1.3
Age-Related Macular Degeneration and Glaucoma 1.1 1.1
Allergic Rhinitis (Hay Fever) 1.5 0.7 1.14
Allergies 0.9 1 -0.11
Allergy to milk products 0.5 0.6 -0.2
Alopecia (Hair Loss) 0.6 0.6
Alzheimer's disease 2.2 2.2 0
Amyotrophic lateral sclerosis (ALS) Motor Neuron 2 0.3 5.67
Ankylosing spondylitis 1.9 0.6 2.17
Anorexia Nervosa 0.6 1.6 -1.67
Antiphospholipid syndrome (APS) 0.3 0.3 0
Asthma 2.5 1.8 0.39
Atherosclerosis 0.7 0.7 0
Atrial fibrillation 1.9 0.9 1.11
Autism 2.7 3.7 -0.37
Autoimmune Disease 0.6 0.8 -0.33
Barrett esophagus cancer 0.3 -0.3
benign prostatic hyperplasia 0.3 -0.3
Biofilm 0.4 0.4
Bipolar Disorder 0.6 0.5 0.2
Brain Trauma 0.6 1.1 -0.83
Cancer (General) 1 -1
Carcinoma 1.7 1.2 0.42
Celiac Disease 0.7 1.9 -1.71
Cerebral Palsy 1 0.8 0.25
Chronic Fatigue Syndrome 1.1 1.9 -0.73
Chronic Kidney Disease 1 1.2 -0.2
Chronic Lyme 0.1 0.8 -7
Chronic Obstructive Pulmonary Disease (COPD) 0.3 1.1 -2.67
Chronic Urticaria (Hives) 0.3 0.4 -0.33
Coagulation / Micro clot triggering bacteria 0.3 0.8 -1.67
Cognitive Function 1.4 1.1 0.27
Colorectal Cancer 2.6 1.1 1.36
Constipation 0.6 0.5 0.2
Coronary artery disease 0.4 1 -1.5
COVID-19 1.5 3.4 -1.27
Crohn's Disease 2.8 3.1 -0.11
Cushing's Syndrome (hypercortisolism) 0.3 -0.3
cystic fibrosis 1.1 -1.1
deep vein thrombosis 0.3 1.1 -2.67
Denture Wearers Oral Shifts 0.3 0.3
Depression 4.3 3.9 0.1
Dermatomyositis 0.3 0.3 0
Eczema 0.4 0.7 -0.75
Endometriosis 1.4 0.8 0.75
Eosinophilic Esophagitis 0.3 -0.3
Epilepsy 1.1 1 0.1
erectile dysfunction 0.3 0.3 0
Fibromyalgia 1.4 0.8 0.75
Functional constipation / chronic idiopathic constipation 1.3 1.3 0
gallstone disease (gsd) 0.8 1 -0.25
Gastroesophageal reflux disease (Gerd) including Barrett's esophagus 0.1 0.6 -5
Generalized anxiety disorder 0.8 1 -0.25
Glioblastoma 0.3 -0.3
Gout 0.7 0.1 6
Graves' disease 0.6 2 -2.33
Gulf War Syndrome 0.3 0.8 -1.67
Halitosis 0.6 0.3 1
Hashimoto's thyroiditis 2 1.3 0.54
Heart Failure 1.3 1 0.3
hemorrhagic stroke 0.6 0.6
Hidradenitis Suppurativa 1.2 1.2
High Histamine/low DAO 0.5 0.3 0.67
hypercholesterolemia (High Cholesterol) 0.3 -0.3
hyperglycemia 0.6 1 -0.67
Hyperlipidemia (High Blood Fats) 0.7 0.7
hypersomnia 0.3 -0.3
hypertension (High Blood Pressure 2.1 2.6 -0.24
Hypothyroidism 0.1 0.3 -2
Hypoxia 1.3 0.3 3.33
IgA nephropathy (IgAN) 0.6 1.7 -1.83
Inflammatory Bowel Disease 1.3 2.6 -1
Insomnia 1.2 1.8 -0.5
Intelligence 0.5 0.5
Intracranial aneurysms 0.3 0.3
Irritable Bowel Syndrome 2.6 2.3 0.13
ischemic stroke 0.9 0.8 0.13
Liver Cirrhosis 2.6 3.3 -0.27
Long COVID 1.3 3 -1.31
Low bone mineral density 0.8 -0.8
Lung Cancer 0.3 0.8 -1.67
Mast Cell Issues / mastitis 0.3 0.3 0
ME/CFS with IBS 0.3 0.7 -1.33
ME/CFS without IBS 0.4 1.3 -2.25
membranous nephropathy 0.3 0.3
Menopause 0.3 0.7 -1.33
Metabolic Syndrome 2.9 3.4 -0.17
Mood Disorders 4 2.7 0.48
multiple chemical sensitivity [MCS] 0.4 0.4
Multiple Sclerosis 1.9 2.3 -0.21
Multiple system atrophy (MSA) 0.4 0.3 0.33
myasthenia gravis 0.3 0.5 -0.67
neuropathic pain 1.6 -1.6
Neuropathy (all types) 0.4 0.5 -0.25
neuropsychiatric disorders (PANDAS, PANS) 0.3 0.3
Nonalcoholic Fatty Liver Disease (nafld) Nonalcoholic 2 1.8 0.11
NonCeliac Gluten Sensitivity 0.8 0.6 0.33
Obesity 4.2 4.6 -0.1
obsessive-compulsive disorder 1.3 1.8 -0.38
Osteoarthritis 0.8 1 -0.25
Osteoporosis 0.8 1.4 -0.75
pancreatic cancer 0.3 0.3 0
Parkinson's Disease 3 3 0
Polycystic ovary syndrome 1.6 1.8 -0.13
Postural orthostatic tachycardia syndrome 0.3 -0.3
Premenstrual dysphoric disorder 0.3 0.3
primary biliary cholangitis 0.9 0.5 0.8
Primary sclerosing cholangitis 0.6 0.1 5
Psoriasis 1 1.1 -0.1
rheumatoid arthritis (RA),Spondyloarthritis (SpA) 3 1.8 0.67
Rosacea 0.3 0.5 -0.67
Schizophrenia 1.9 1.5 0.27
scoliosis 0.9 -0.9
Sjögren syndrome 0.3 1.3 -3.33
Sleep Apnea 1.2 0.8 0.5
Slow gastric motility / Gastroparesis 0.3 0.3 0
Small Intestinal Bacterial Overgrowth (SIBO) 0.6 0 0
Stress / posttraumatic stress disorder 1.8 1.4 0.29
Systemic Lupus Erythematosus 1.1 1.7 -0.55
Tic Disorder 0.3 0.9 -2
Tourette syndrome 1 0.3 2.33
Type 1 Diabetes 1.3 2.1 -0.62
Type 2 Diabetes 2.6 3.1 -0.19
Ulcerative colitis 1.9 2.2 -0.16
Unhealthy Ageing 1.8 1 0.8
Vitiligo 1.3 0.4 2.25

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