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Chinese Journal of Diagnostics(Electronic Edition) ›› 2017, Vol. 05 ›› Issue (02): 120-123. doi: 10.3877/cma.j.issn.2095-655X.2017.02.011

Special Issue:

• Clinical Study • Previous Articles     Next Articles

Diagnostic value of serum levels of acylated ghrelin and nesfatin-1 in adult patients with primary epilepsy

Min Xia1, Dong Liu1, Yanling Wang1, Xu Chu1, Qingxia Kong1,()   

  1. 1. Department of Neurology, Affiliated Hospital of Jining Medical University, Jining 272029, China
  • Received:2016-12-13 Online:2017-05-26 Published:2017-05-26
  • Contact: Qingxia Kong
  • About author:
    Corresponding author: Kong Qingxia, Email:

Abstract:

Objective

To study the serum levels of acylated ghrelin(AG)and nesfatin-1 in adult patients with primary epilepsy in the pretreatment period and six months after carbamazepine (CBZ) or valproic acid(VPA) therapy.

Methods

Fifty adult patients with primary epilepsy [30 with secondary generalized epilepsy (SGE), 20 with primary generalized epilepsy (PGE)] and 20 control patients were included in this study.Serum levels of AG and nesfatin-1 were measured in these groups in the pretreatment period and six months after treatment.

Results

Serum level of AG in control group was (42.49±8.24) ng/L, pretherapy serum level of AG in SGE (32.67±5.64)ng/L was lower than that in control group (t=2.08, P<0.05). Post-CBZ therapy serum level of AG (54.31±7.91)ng/L was higher than that in pretherapy (t=2.80, P<0.05). Pretherapy serum level of AG in PGE (31.56±6.32)ng/L was lower than that in control group(t=2.09, P<0.05), post-VPA therapy serum level of AG (51.37±7.56)ng/L was higher than that in pretherapy(t=3.22, P<0.05). Serum level of nesfatin-1 in control group was (0.66±0.02)μg/L.Pretherapy serum level of nesfatin-1 in SGE [(6.57±0.93)μg/L] was higher than that in control group(t=2.18, P<0.05), post-CBZ therapy serum level of nesfatin-1 [(2.74±0.56)μg/L] was also higher than that in control group(t=2.05, P<0.05). Pretherapy serum level of nesfatin-1 in PGE (9.04±1.32)μg/L was higher than that in control group (t=3.83, P<0.05), post-VPA therapy serum level of nesfatin-1(3.28±0.43)μg/L was also higher than that in control group (t=2.24, P<0.05).

Conclusion

AG may have protective effects on neurons and have antiepilepsy effects, nesfatin-1 may serve as biomarker for the diagnosis of primary epilepsy.

Key words: Epilepsy, Neuropeptides, Carbamazepine, Valproic acid

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