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Blutwerte · Marker

Apolipoprotein A1

ApoA1 · Apo A-I

Lipide & Herz-Kreislauf
Einheit:
g/L
Abbreviation
ApoA1

Apolipoprotein A1 quantifies the major protein component of HDL particles involved in lipid transport and metabolism.

Reference Ranges

Reference
1.251.6g/L
1.25
1.2
1.8
1.6
LowNormalHigh
Reference
Optimal
Unit · g/L

ApoA1 levels are not significantly affected by fasting status.

Overview

Übersicht

Apolipoprotein A1 (ApoA1) is a major protein component of high-density lipoprotein (HDL) in plasma and plays a crucial role in lipid metabolism. It is primarily responsible for the activation of lecithin-cholesterol acyltransferase (LCAT), an enzyme that converts free cholesterol into cholesteryl ester, a more hydrophobic form of cholesterol that is sequestered into the core of the HDL particle. Clinically, ApoA1 is considered a marker of cardiovascular health, as higher levels are associated with a reduced risk of atherosclerotic cardiovascular disease. Researchers found that ApoA1 levels are not significantly affected by fasting status, making it a reliable marker in both fasting and non-fasting states. In the context of athletic performance and biohacking, ApoA1 is of interest due to its role in cholesterol transport and potential implications for cardiovascular endurance and longevity. Elevated ApoA1 levels are generally considered beneficial, as they reflect efficient reverse cholesterol transport and anti-inflammatory properties. However, researchers observed that in certain pathological conditions, such as liver failure or cryoglobulinemia, ApoA1 levels can be altered, which may confound its interpretation. Additionally, while fasting is not required for ApoA1 measurement, it is important to consider factors such as acute illness or chronic inflammation that could affect levels.

Klinische Bedeutung

Elevated ApoA1 levels are associated with a lower risk of cardiovascular disease, reflecting efficient cholesterol efflux and anti-inflammatory properties. Reduced levels may indicate increased cardiovascular risk or liver dysfunction.

Dynamics

Trend Interpretation

Rising Values

Progressively rising ApoA1 levels suggest improved cardiovascular health. Retest annually to monitor trends.

Falling Values

Progressively falling ApoA1 levels may indicate increased cardiovascular risk or liver dysfunction.

Re-test Interval

4 weeks if outside optimal range

Etiology

Causes — High & Low

Cause

Elevated Levels

  • Genetic factors
  • Regular physical activity
  • High HDL cholesterol levels
  • Certain medications (e.g., statins)
Cause

Low Levels

  • Liver disease
  • Chronic inflammation
  • Malnutrition
  • Metabolic syndrome
Protocol

How to Optimize

Lever

Lifestyle

  • Regular aerobic exercise
  • Smoking cessation
  • Weight management
Lever

Nutrition

  • Increase intake of omega-3 fatty acids
  • Consume a diet rich in fruits and vegetables
  • Limit saturated fat intake
Lever

Supplementation

  • Niacin
  • Fish oil

Note:

Consult a healthcare provider before starting any supplementation, especially if you have underlying health conditions.

Testing Guidelines

Fasting Not Required
Not Time-Sensitive

Testing Frequency

Annually for cardiovascular risk assessment

Interfering Factors

  • Acute illness
  • Chronic inflammation

Related Peptides & Hormones

Hdl Cholesterol

Correlated with

hormone or peptide

Open Research Questions

Current research suggests that reference ranges for apolipoprotein A1 (ApoA1) and its optimal targets in various clinical contexts, such as liver disease and cryoglobulinemia, remain debated. Researchers have not yet established the specific confounders affecting ApoA1 levels, particularly in non-fasting versus fasting states. Additionally, unanswered clinical questions include the precise role of ApoA1 in immune function and its potential as a therapeutic target in atherosclerosis and other lipid metabolism disorders.

31 Research Publications

1,157

Total Citations

20

Human/RCT

7.4

Avg. Influence

2025

Latest

Sort
Filter
#01

Fasting is not routinely required for determination of a lipid profile: clinical and laboratory implications including flagging at desirable concentration cut-points-a joint consensus statement from the European Atherosclerosis Society and European Federation of Clinical Chemistry and Laboratory Medicine.

HumanInfluence33.0
819
Researchers found that fasting status does not significantly affect the concentrations of apolipoprotein A1 and other lipid profile components. The study recommends using non-fasting lipid profiles for routine assessments, which can improve patient compliance without compromising the accuracy of cardiovascular risk predictions.
View on PubMed
#02

Blood-based biomarkers for Parkinson's disease.

ReviewInfluence1.0
141
Researchers discussed the potential of Apolipoprotein A1 (APOA1) as a blood-based biomarker for Parkinson's disease, among other candidates. They highlighted the challenges and advancements in identifying effective biomarkers from blood samples.
View on PubMed
#03

Apolipoprotein A1 and B.

ReviewInfluence1.0
49
This article reviewed the superiority of apolipoproteins A1 and B over traditional cholesterol measures in assessing vascular disease risk. Researchers highlighted the importance of these biomarkers in laboratory practices and their relevance in monitoring lipid-lowering therapies.
View on PubMed
#04

Serum apolipoprotein A-I depletion is causative to silica nanoparticles-induced cardiovascular damage.

Animal
48
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.
View on PubMed
#05

HDLs and the pathogenesis of atherosclerosis.

Schwertani Adel, et al. · Current opinion in cardiology · 2018

Review
18
This review explored the role of HDL and apolipoprotein A1 in atherosclerosis. Researchers found that HDL's protective functions can be compromised in disease states, suggesting that changes in Apo A-I may contribute to the progression of cardiovascular diseases.

Key findings

  1. 01Researchers observed that HDL cholesterol levels are not effective therapeutic targets for preventing heart disease.
  2. 02They found that HDL performs various protective functions against atherosclerosis that are independent of cholesterol levels.
  3. 03The study identified a protein, desmocollin 1, that may hinder HDL's beneficial roles in heart health.
View on PubMed
#06

HDL Structure.

Review
17
This study examined the structure and function of high-density lipoprotein (HDL), highlighting the role of apolipoprotein A1 (Apo A-I) as a major component. Researchers found that HDL is involved in various physiological processes and that its structure can change under different conditions, affecting its function in lipid metabolism and immune response.
View on PubMed
#07

HDL-cholesterol confers sensitivity of immunotherapy in nasopharyngeal carcinoma via remodeling tumor-associated macrophages towards the M1 phenotype.

Human
11
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.
View on PubMed
#08

ApoA1/HDL and sepsis-associated vascular endothelial injury: a narrative review.

Guo Kailin, et al. · Critical care (London, England) · 2025

ReviewInfluence1.0
9
This review focused on the role of apolipoprotein A1 in sepsis-related vascular injury. Researchers found that decreased levels of Apo A-I are linked to endothelial damage, suggesting its potential as a therapeutic target for improving vascular health in sepsis.

Key findings

  1. 01Researchers observed a strong connection between decreased ApoA1/HDL levels and endothelial damage during infections.
  2. 02They identified three protective mechanisms of ApoA1: reducing inflammation, maintaining blood vessel integrity, and restoring blood flow.
  3. 03The review suggests that therapies based on ApoA1, such as mimetic peptides and recombinant HDL, could be promising for treating sepsis.
View on PubMed
#09

Association between serum apolipoprotein B and atrial fibrillation: a case-control study.

Human
8
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.
View on PubMed
#10

APOA1 mRNA and serum APOA1 protein as diagnostic and prognostic biomarkers in gastric cancer.

Human
8
Researchers explored the prognostic value of Apolipoprotein A1 (APOA1) in gastric cancer, finding that lower levels were linked to poor prognosis. The study suggests that APOA1 could serve as a diagnostic and prognostic biomarker in managing gastric cancer.
View on PubMed

Clinical Trials (2)

2

Total Trials

2,050

Total Enrolled

Effects of 10 Weeks of Lifestyle Coaching on Cardiometabolic Risk Factors, Workability and Subjective Wellbeing

Sponsor

Aava Medical

Enrollment

2,000

Started

2020

Primary outcome

ApoB/ApoA1

Work Related StressMetabolic SyndromeLipid Metabolism DisordersLifestyle Risk ReductionBurnout

Resveratrol and Serum Apo A-I

NCT01364961COMPLETED
Sponsor

Maastricht University Medical Center

Enrollment

50

Started

2011

Primary outcome

ApoA-I level

Dyslipidemia

Publication Trend

Research publications about Apolipoprotein A1 over time

10total
1
'99
1
'06
1
'16
1
'18
2
'22
4
'25

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