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ApoA1 · Apo A-I
Apolipoprotein A1 quantifies the primary protein component of HDL involved in cholesterol transport.
Ranges may vary slightly based on laboratory standards. Fasting is recommended.
Apolipoprotein A1 (ApoA1) is a major protein component of high-density lipoprotein (HDL) in plasma, playing a crucial role in lipid metabolism. It is involved in the reverse transport of cholesterol from tissues to the liver for excretion. Researchers have found that ApoA1 is a key factor in conferring atheroprotective properties to HDL, including cholesterol efflux capacity and anti-inflammatory effects. Clinically, ApoA1 levels are used as a biomarker for cardiovascular health, with low levels associated with increased risk of atherosclerotic cardiovascular disease. It is also considered a protective factor in conditions like acute-on-chronic liver failure (ACLF), where it is linked to improved short-term prognosis. In the context of athletic performance and longevity, ApoA1 is of interest due to its role in maintaining cardiovascular health and potentially influencing lipid metabolism efficiency. However, researchers observed that factors such as age, disease states, and genetic variations can alter ApoA1 levels and its functional properties, which may confound its interpretation. Fasting is generally recommended for accurate measurement, as lipid levels can be influenced by recent food intake.
Klinische Bedeutung
Reduced ApoA1 levels indicate increased cardiovascular risk and may reflect impaired lipid metabolism. Elevated levels are generally protective, associated with reduced risk of atherosclerosis.
Progressively rising ApoA1 values suggest improved cardiovascular protection. Re-test annually to monitor trends.
Progressively falling ApoA1 values may indicate increased cardiovascular risk.
Re-test Interval
4 weeks if outside optimal range
Note:
Consult a healthcare provider before starting any supplementation.
Testing Frequency
Annually for adults at risk of cardiovascular disease
Correlated with
Current research suggests that reference ranges and optimal targets for apolipoprotein A1 (APOA1) remain debated, particularly in the context of various diseases such as HBV-related acute-on-chronic liver failure and cryoglobulinemia. Researchers have not yet established the precise confounders affecting APOA1 levels, nor the specific mechanisms by which it influences immune function and disease progression. Unanswered clinical questions include the role of APOA1 in therapeutic strategies for cardiovascular diseases and its potential as a prognostic marker across different populations.
187
Total Citations
16
Human/RCT
1.0
Avg. Influence
2025
Latest
This article reviewed evidence suggesting that Apolipoprotein A1 (ApoA1) and Apolipoprotein B (ApoB) are more reliable indicators of vascular disease risk compared to traditional cholesterol measurements. Researchers highlighted their potential in clinical laboratory practice.
Researchers found that silica nanoparticles can deplete Apolipoprotein A1 (ApoA1) from the bloodstream, leading to cardiovascular damage. The study suggests that maintaining ApoA1 levels may be important for mitigating the toxic effects of nanoparticle exposure.
Schwertani Adel, et al. · Current opinion in cardiology · 2018
Researchers reviewed the role of HDL cholesterol in cardiovascular health, noting that while it serves as a biomarker, its therapeutic modulation has not proven effective in preventing atherosclerosis. The study emphasized that HDL's beneficial properties can diminish in disease states.
Key findings
This study examined the structure and components of high-density lipoprotein (HDL), highlighting the role of Apolipoprotein A1 (Apo A-I) as a key protein involved in HDL function. Researchers found that HDL is crucial in various physiological processes, and its structural features can change in different health conditions.
Researchers found that higher levels of Apolipoprotein A1 (ApoA1) and HDL cholesterol were associated with improved responses to immunotherapy in nasopharyngeal carcinoma patients. The study suggested that ApoA1 mimetics could enhance therapeutic outcomes by modulating macrophage polarization.
This study identified Apolipoprotein A1 (APOA1) as a potential prognostic biomarker in gastric cancer, showing that lower serum levels correlated with poor outcomes. Researchers emphasized the role of lipid metabolism alterations in tumor progression.
This study examined the association between Apolipoprotein B (ApoB) levels and atrial fibrillation (AF). Researchers found that lower ApoB levels were linked to a protective effect against AF in both men and women, indicating its potential as a biomarker.
This study examined the relationship between METTL14 expression and coronary heart disease (CHD). Researchers found that higher METTL14 levels were associated with increased inflammatory markers and could independently predict CHD risk.
Researchers found that a common polymorphism in the Apolipoprotein A1 gene is associated with an increased risk of recurrent coronary events in Black patients post-myocardial infarction. This suggests ethnic differences in genetic risk factors for coronary artery disease.
This study identified cholesterol metabolism-related genes, including Apolipoprotein A1 (ApoA1), as independent prognostic factors in gastric cancer. Researchers found that these genes could predict patient outcomes and immune cell variations, highlighting their significance in cancer treatment.
Research publications about Apolipoprotein A1 over time
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