Paraoxonase 55 and 192 polymorphism and its relationship to serum paraoxonase activity and serum lipids in Turkish patients with non-insulin dependent diabetes mellitus


Agachan B., YILMAZ H., KARAALI Z., ISBIR T.

CELL BIOCHEMISTRY AND FUNCTION, cilt.22, sa.3, ss.163-168, 2004 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 22 Sayı: 3
  • Basım Tarihi: 2004
  • Doi Numarası: 10.1002/cbf.1070
  • Dergi Adı: CELL BIOCHEMISTRY AND FUNCTION
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.163-168
  • Anahtar Kelimeler: paraoxonase, polymorphism, activity, lipid, NIDDM, Turkish, CORONARY-ARTERY-DISEASE, MYOCARDIAL-INFARCTION, PLASMA-LIPOPROTEINS, MOLECULAR-BASIS, HEART-DISEASE, GENE, RISK, ARYLESTERASE, LEU-MET54, HUMPONA
  • İstanbul Üniversitesi Adresli: Evet

Özet

We investigated the effect of PON 55 and PON 192 polymorphisms on serum PON1 activity and lipid profiles in 213 non-insulin dependent diabetes mellitus (NIDDM) individuals and 116 non-diabetic controls among Turkish subjects. The distribution of PON 55/192 gene polymorphism was determined by polymerase chain reaction-based restriction fragment length polymorphism. Serum lipid levels were measured enzymically. PON activity was measured by spectrophotometric assay of p-nitrophenol production following addition of paraoxon. We found that PON 55 and 192 genotype distribution was similar in patients and controls and paraoxonase activity was generally lower in diabetics than in control subjects. We showed that PON 55 and 192 genotypes have a major effect on serum PON activity. PON 192 BB homozygotes had significantly higher PON activity than AA and AB genotypes among the control and NIDDM populations (p < 0.001). PON 55 MM homozygotes had significantly lower PON activity than did LL and LM genotypes in control and NIDDM populations (p < 0.05). The PON1 55 and 192 polymorphisms did not consistently influence the serum lipid profiles in either population. In conclusion, our results suggest that the paraoxonase activities are affected by PON I genetic variability in Turkish NIDDM patients and controls. Copyright (C) 2004 John Wiley Sons, Ltd.