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Published on: June 9, 2018
Gene polymorphisms and serum alpha-2-Heremans-Schmid levels in Italian haemodialysis patients
Mario Cozzolino1, Maria Luisa Biondi, Andrea Galassi
1Renal Division, S. Paolo Hospital, University of Milan, Milan, Italy. mariocozzolino@hotmail.com
Insights
Serum fetuin-A levels are reduced in Italian hemodialysis patients. However, this reduction is not linked to AHSG gene polymorphisms, suggesting other factors influence cardiovascular risk in these patients.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Genetics
Background:
- Vascular calcification (VC) and atherosclerosis are leading causes of cardiovascular (CV) morbidity and mortality in hemodialysis (HD) patients.
- Fetuin-A (alpha(2)-Heremans-Schmid glycoprotein, AHSG) is a protein that inhibits VC and has been linked to inflammation and CV mortality in HD patients.
Purpose of the Study:
- To investigate the association between serum fetuin-A levels and AHSG gene polymorphisms in an Italian HD population.
- To explore the role of fetuin-A in cardiovascular risk in chronic kidney disease (CKD) patients undergoing HD.
Main Methods:
- Genotyping of the AHSG (T256S) common polymorphisms in 96 HD patients and 57 healthy controls.
- Measurement of serum fetuin-A levels in both groups.
Main Results:
- Serum fetuin-A levels were significantly lower in HD patients (0.35 +/- 0.11 g/l) compared to healthy controls (0.62 +/- 0.31 g/l).
- No significant association was found between low serum fetuin-A levels and the Ser/Ser genotype of the AHSG gene in either HD patients or controls.
- The distribution of AHSG gene polymorphisms was similar between HD patients and healthy controls.
Conclusions:
- Italian HD patients exhibit reduced serum fetuin-A levels compared to healthy individuals.
- The reduction in serum fetuin-A in this HD population is not associated with alterations in AHSG T256S polymorphism distribution.
- CKD patients on HD may have similar AHSG gene polymorphism distribution to the general population.
Background:
Vascular calcification (VC) and accelerated atherosclerosis are major causes of cardiovascular (CV) morbidity and mortality in haemodialysis (HD) patients. Inhibitory proteins are associated with reduced VC and may play a key role in preventing CV in chronic kidney disease (CKD) patients. Fetuin-A, also known as alpha(2)-Heremans-Schmid glycoprotein (AHSG), is a circulating plasma protein with inhibitory effects on VC that has been associated with inflammation and CV mortality in HD patients. In the present study, we investigated the associations between serum fetuin-A levels and its gene (AHSG) polymorphisms in an Italian HD population.
Methods:
Ninety-six patients on stable chronic HD treatment and 57 healthy controls were genotyped for the common polymorphisms on the AHSG (T256S). In addition, serum fetuin-A levels were tested.
Results:
In this study, serum fetuin-A levels were lower in HD patients (0.35 +/- 0.11 g/l) compared with healthy controls (0.62 +/- 0.31 g/l, p < 0.05). In both HD patients and the control group, the distribution of the AHSG gene did not show significant association between low serum fetuin-A levels and the Ser/Ser genotype, known to be associated with a higher CV mortality risk in the HD population. Moreover, the distribution of AHSG gene polymorphisms in HD patients and in healthy controls was similar.
Conclusions:
In contrast with previous reports, this study suggests that CKD patients on HD treatment have a similar polymorphism distribution of the AHSG gene compared with the normal population and that the reduction in serum fetuin-A levels in Italian HD patients is not associated with an alteration in the distribution of AHSG T256S polymorphisms.
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