» Articles » PMID: 22340510

Serum Bilirubin and Lipoprotein-a: How Are These Associated with Whole Blood Viscosity?

Overview
Journal Redox Rep
Date 2012 Feb 21
PMID 22340510
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Background: It has been demonstrated that oxidative stress can induce red blood cell rigidity and haemolysis, which in turn can cause hyperviscosity and hyperbilirubinaemia, respectively. However, haemolysis may be associated with a low level of haemoglobin, which reduces whole blood viscosity (WBV). Bilirubin can behave as antioxidant or oxidant, and one uncharted course for diagnostic pathology is how or whether bilirubinaemia and viscosity are associated. Further, oxidative stress is now being assessed using lipoprotein-a (Lp(a)), among other things but whether it is associated with blood viscosity has not been established.

Aim: This study investigates the association and correlation of haemoglobin level and WBV with serum Lp(a) and bilirubin levels in a general population of patients.

Materials And Methods: Sixty-eight cases that were tested for Lp(a), concomitantly with full blood count and liver function, in our archived clinical pathology database were used in this study. WBV levels were determined using a validated formula. Multivariate and univariate analyses as well as correlation were performed.

Results: WBV was found to be significantly associated with bilirubin (P<0.02), but not with Lp(a). Haemoglobin concentration was inversely correlated with Lp(a) (P<0.04), but not with bilirubinaemia.

Conclusion: This pilot study suggests that hyperbilirubinaemia and hyperviscosity are associated and positively correlated. Consideration of whether serum bilirubin (as an indirect index of oxidative stress) can be used in combination with WBV (as index of macrovascular effect of oxidative stress) to assess oxidative damage is recommended.

Citing Articles

Blood Viscosity Changes in Diabetes Mellitus: A 20-Year Bibliometric Review and Future Directions.

Mbah J, Bwititi P, Gyawali P, Nwose E Cureus. 2024; 16(7):e64211.

PMID: 39130872 PMC: 11310740. DOI: 10.7759/cureus.64211.


Relationship between lipoprotein(a) and whole blood reducing viscosity: A cross-sectional study.

Jing S, Zhu H Medicine (Baltimore). 2023; 102(48):e36236.

PMID: 38050213 PMC: 10695618. DOI: 10.1097/MD.0000000000036236.


Changes in the Blood Viscosity in Patients With SARS-CoV-2 Infection.

Al-Kuraishy H, Al-Gareeb A, Al-Hamash S, Cavalu S, El-Bouseary M, Sonbol F Front Med (Lausanne). 2022; 9:876017.

PMID: 35783600 PMC: 9247235. DOI: 10.3389/fmed.2022.876017.


Hyperviscosity syndrome in COVID-19 and related vaccines: exploring of uncertainties.

Al-Kuraishy H, Al-Gareeb A, El-Bouseary M, Sonbol F, El-Saber Batiha G Clin Exp Med. 2022; 23(3):679-688.

PMID: 35608715 PMC: 9128329. DOI: 10.1007/s10238-022-00836-x.


Bilirubin as an indicator of cardiometabolic health: a cross-sectional analysis in the UK Biobank.

Seyed Khoei N, Wagner K, Sedlmeier A, Gunter M, Murphy N, Freisling H Cardiovasc Diabetol. 2022; 21(1):54.

PMID: 35436955 PMC: 9017025. DOI: 10.1186/s12933-022-01484-x.


References
1.
Barghash N, Elewa S, Hamdi E, Barghash A, El Dine R . Role of plasma homocysteine and lipoprotein (a) in coronary artery disease. Br J Biomed Sci. 2004; 61(2):78-83. DOI: 10.1080/09674845.2004.11732648. View

2.
Matteucci E, Giampietro O . Oxidative stress in families of type 1 diabetic patients. Diabetes Care. 2000; 23(8):1182-6. DOI: 10.2337/diacare.23.8.1182. View

3.
Merrill E, GILLILAND E, COKELET G, Shin H, Britten A, WELLS Jr R . Rheology of human blood, near and at zero flow. Effects of temperature and hematocrit level. Biophys J. 1963; 3:199-213. PMC: 1366440. DOI: 10.1016/s0006-3495(63)86816-2. View

4.
Roll E, Christensen T . Formation of photoproducts and cytotoxicity of bilirubin irradiated with turquoise and blue phototherapy light. Acta Paediatr. 2005; 94(10):1448-54. DOI: 10.1111/j.1651-2227.2005.tb01819.x. View

5.
Marcovina S, Albers J, Scanu A, Kennedy H, Giaculli F, Berg K . Use of a reference material proposed by the International Federation of Clinical Chemistry and Laboratory Medicine to evaluate analytical methods for the determination of plasma lipoprotein(a). Clin Chem. 2000; 46(12):1956-67. View