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Exploring the Potential of Finger Prick Blood for Assessment of BIOmarkers for LOw Grade Inflammation and CVD Risk

Exploring the Potential of Finger Prick Blood for Assessment of BIOmarkers for LOw Grade Inflammation and CVD Risk

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04996589
Acronym
BIOLOGIC
Enrollment
10
Registered
2021-08-09
Start date
2021-07-08
Completion date
2021-07-27
Last updated
2021-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Biomarker

Keywords

LPS, biomarker, finger prick test, postprandial

Brief summary

There are currently no minimally invasive techniques for the measurement of lipopolysaccharide (LPS) and Apo-B48 that can be used in samples collected in field settings. In this project we want to explore whether postprandial assessment of biomarkers LPS and ApoB48 in blood withdrawn with a finger prick test can be used as marker for low grade inflammation and risk factor for CVD. The primary objectives of this pilot study are to a) determine whether postprandial LPS and ApoB48 levels can be assessed in finger prick blood of both lean subjects and obese subjects; and b) compare postprandial LPS and ApoB48 levels assessed in venous blood and blood collected through a finger prick test. This study is an observational pilot study in which postprandial LPS and ApoB48 will be assessed before and after ingestion of a high fat load in 5 lean and 5 obese subjects in the age range 18-70 years. Samples will be collected under fasting conditions and in response to a high fat challenge test (1, 2, 4 and 6 hours post ingestion). The risks for participation are very small if not negligible. No adverse effects of the high fat challenge were reported previously. Consumption of high amounts of saturated fat may cause some GI discomfort. Blood sampling will be performed via a cannula and the insertion can be a painful and may cause a bruise. Finger prick might also give a short pain sensation and small bruises. The amount of blood that is drawn from participants is relatively small (total 37.5 ml) and is therefore within acceptable limits. There are no direct benefits for the participants. In the BIOLOGIC study we include both lean subjects and obese subjects as we expect differences in postprandial responses related to differences in chylomicron production and LPS levels. Therefore it is important to explore these biomarkers in both target groups. This study can therefore be regarded as group-related, non-therapeutic research.

Interventions

None listed

Sponsors

Wageningen University and Research
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

Inclusion criteria

* Age 18-70 years * Living in the surroundings of Wageningen (max. 25 km) * Stable body weight for past 6 months * Suitable veins for insertion of cannula * BMI 18.5-22 kg/m2 (lean subjects) * BMI ≥ 30 kg/m2 (obese subjects)

Exclusion criteria

* Use of cholesterol-lowering medication (e.g. statins) * Use of diabetes medication (e.g. insulin, metformin) * Use of antibiotics or anti-inflammatory medication (e.g. NSAIDS such as ibuprofen) * Known allergy for any of the food components used in the study (milk, cream, sugars) * Blood clotting disorders * Current smokers * Alcohol consumption of \> 21 units per week * Participation in another clinical trial at the same time * Being an employee of Wageningen Food & Biobased Research

Design outcomes

Primary

MeasureTime frameDescription
ApoB48_6-26 hours post ingestionSerum levels ApoB48 finger prick blood after high-fat shake intake
LPS1-21 hour post ingestionSerum levels LPS finger prick blood after high-fat shake intake
ApoB48_1-21 hour post ingestionSerum levels ApoB48 finger prick blood after high-fat shake intake
LPS2-12 hours post ingestionSerum levels LPS venous blood samples after high-fat shake intake
ApoB48_2-12 hours post ingestionSerum levels ApoB48 venous blood samples after high-fat shake intake
LPS2-22 hours post ingestionSerum levels LPS finger prick blood after high-fat shake intake
ApoB48_2-22 hours post ingestionSerum levels ApoB48 finger prick blood after high-fat shake intake
LPS4-14 hours post ingestionSerum levels LPS venous blood samples after high-fat shake intake
ApoB48_4-14 hours post ingestionSerum levels ApoB48 venous blood samples after high-fat shake intake
ApoB48_6-16 hours post ingestionSerum levels ApoB48 venous blood samples after high-fat shake intake
LPS6-26 hours post ingestionSerum levels LPS finger prick blood after high-fat shake intake
LPS4-24 hours post ingestionSerum levels LPS finger prick blood after high-fat shake intake
ApoB48_4-24 hours post ingestionSerum levels ApoB48 finger prick blood after high-fat shake intake
LPS6-16 hours post ingestionSerum levels LPS venous blood samples after high-fat shake intake
LPS_B1BaselineSerum levels LPS venous blood samples under fasting conditions
ApoB48_B1BaselineSerum levels ApoB48 venous blood samples under fasting conditions
LPS_B2BaselineSerum levels LPS finger prick blood under fasting conditions
ApoB48_B2BaselineSerum levels ApoB48finger prick blood under fasting conditions
LPS1-11 hour post ingestionSerum levels LPS venous blood samples after high-fat shake intake
ApoB48_1-11 hour post ingestionSerum levels ApoB48 venous blood samples after high-fat shake intake

Secondary

MeasureTime frameDescription
LBP_11 hour post ingestionPlasma LBP levels in venous blood samples after high-fat shake intake
LBP_22 hours post ingestionPlasma LBP levels in venous blood samples after high-fat shake intake
LBP_44 hours post ingestionPlasma LBP levels in venous blood samples after high-fat shake intake
LBP_66 hours post ingestionPlasma LBP levels in venous blood samples after high-fat shake intake
sCD14_BBaselinePlasma sCD14 levels in venous blood samples collected under fasting conditions
sCD14_11 hour post ingestionPlasma sCD14 levels in venous blood samples after high-fat shake intake
sCD14_22 hours post ingestionPlasma sCD14 levels in venous blood samples after high-fat shake intake
sCD14_44 hours post ingestionPlasma sCD14 levels in venous blood samples after high-fat shake intake
sCD14_66 hours post ingestionPlasma sCD14 levels in venous blood samples after high-fat shake intake
LBP_BBaselinePlasma LBP levels in venous blood samples collected under fasting conditions

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026