Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy


İNCECİK F. , AVCIOGLU G., EREL O., NESELIOGLU S., HERGUNER O. M.

ACTA NEUROLOGICA BELGICA, cilt.119, ss.215-218, 2019 (SCI İndekslerine Giren Dergi) identifier identifier

  • Cilt numarası: 119 Konu: 2
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1007/s13760-018-01072-5
  • Dergi Adı: ACTA NEUROLOGICA BELGICA
  • Sayfa Sayısı: ss.215-218

Özet

Duchenne muscular dystrophy (DMD) is a disorder that alter the expression of the dystrophin protein. Dystrophin deficiency alters the structural integrity of the contractile apparatus/sarcolemmal integrity, leading to dystrophic changes. Dystrophin deficiency results in an increase in oxidative stress. We aimed to investigate the thiol/disulfide balance as an oxidative stress marker in children with DMD. We included 24 DMD, and 22 healthy control group subjects in the study. The total thiol, native thiol, and disulphide levels were measured and the disulphide/native thiol, disulphide/total thiol and native thiol/total thiol ratios were calculated in DMD patients and healthy subjects. The mean age distribution of the patients and the healthy control group subjects was similar. The total thiol, native thiol, and disulfide levels were lower in DMD group than the healthy controls. In conclusion, the markers and ratios were measured and calculated in the blood, and we detected that the total thiol, and native thiol levels were lower in DMD group than the healthy controls. These results indicate that dynamic thiol-disulphide homeostasis can be used as a marker of oxidative stress in clinical trials with DMD.