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DOI 10.1016/j.cca.2016.06.010

Медицинская библиотека · Clinica chimica acta; international journal of clinical chemistry · 2016

Value of serum human epididymis secretory protein 4 as a marker for differential diagnosis of malignant and benign gynecological diseases of patients in southern China.

Li Laisheng, Wan Jianxin, Cai Gaorong, Yuan Linjing, Liang Jianbo, Song Junli, Wang Fen, Liu Min

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Аннотация

BACKGROUND

This study investigated the clinical value of HE4 in distinguishing malignant and benign gynecological diseases of patients in southern China.

METHODS

Preoperative serum CA125 and HE4 concentrations were tested in samples of women with malignant or benign gynecological diseases using fully automated methods (Abbott ARCHITECT) and validated cutoff values.

RESULTS

For the discrimination of ovarian cancer from benign gynecological diseases, in premenopausal women, the sensitivity and specificity were 89.8% and 67.5% for CA125, 68.5% and 97.8% for HE4, and 88.9% and 78.6% for ROMA, whereas in postmenopausal women, the sensitivity and specificity were 86.6% and 88.9% for CA125, 57.3% and 100% for HE4, and 85.4% and 94.4% for ROMA. For the discrimination of endometrial cancer from benign gynecological diseases, in premenopausal women, the sensitivity and specificity were 20.3% and 67.5% for CA125, 56.8% and 97.8% for HE4, and 74.3% and 78.6% for ROMA, whereas in postmenopausal women, the sensitivity and specificity were 17.8% and 88.9% for CA125, 31.5% and 100% for HE4, and 32.9% and 94.4% for ROMA.

CONCLUSIONS

We showed that HE4 had better specificity than CA125 in discriminating ovarian cancer, and endometrial cancer from benign gynecological diseases in southern China population.

Для цитирования: Li Laisheng, Wan Jianxin, Cai Gaorong, Yuan Linjing, Liang Jianbo, Song Junli, Wang Fen, Liu Min. Value of serum human epididymis secretory protein 4 as a marker for differential diagnosis of malignant and benign gynecological diseases of patients in southern China.. Clinica chimica acta; international journal of clinical chemistry. 2016. DOI: 10.1016/j.cca.2016.06.010.

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