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DOI 10.1080/08941939.2016.1257667

Медицинская библиотека · Journal of investigative surgery : the official journal of the Academy of Surgical Research · 2016

Diagnostic Value of High-Mobility Group Box 1 (HMGB1) Protein in Acute and Perforated Appendicitis.

Alizadeh Shabanali, Ghazavi Ali, Ganji Ali, Mosayebi Ghasem

Сравнительное исследованиеОценочное исследованиеСтатьяПеревод пока не подготовлен

Аннотация

AIM: Acute appendicitis is the most common cause of abdominal surgical emergencies. Early diagnosis of appendicitis can reduce perforation and mortality rate. High-mobility group box 1 (HMGB1) protein has been identified as a pro-inflammatory factor and its elevated serum levels have been noted in different diseases. So, the aim of this study was to determine the serum levels of HMGB1 in patients with acute and perforated appendicitis in compare to normal appendix.

MATERIAL AND

METHODS

For this purpose, serum samples were obtained from 81 patients with primary criteria-based appendicitis 6 hr before and 72 hr after appendectomy, in which serum levels of HMGB1 were analyzed by enzyme-linked immunosorbent assay.

RESULTS

The levels of HMGB1 in patients with perforated appendicitis were significantly (p =.045) higher than in patients with acute appendicitis and normal appendix (p =.001) before appendectomy. Serum levels of HMGB1 were increased 72 hr after appendectomy in all the groups (p =.03) compared with the serum levels before appendectomy.

CONCLUSIONS

Since the serum levels of HMGB1 in patients with acute and perforated appendicitis were higher than in patients with normal appendix, these findings could be useful to develop a new biomarker along with other laboratory tests for accurate diagnosis of patients with appendicitis.

Для цитирования: Alizadeh Shabanali, Ghazavi Ali, Ganji Ali, Mosayebi Ghasem. Diagnostic Value of High-Mobility Group Box 1 (HMGB1) Protein in Acute and Perforated Appendicitis.. Journal of investigative surgery : the official journal of the Academy of Surgical Research. 2016. DOI: 10.1080/08941939.2016.1257667.

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