Open Access

Determination of reference intervals of serum levels of human epididymis protein 4 (HE4) in Chinese women

  • Yaping Tian1Email author,
  • Chuanxin Wang2,
  • Liming Cheng3,
  • Aimin Zhang4,
  • Wen Liu5,
  • Lin Guo6,
  • Huiming Ye7,
  • Yanchun Huang8,
  • Jing Chen9,
  • Xinyu Wen1,
  • Yuelei Xing1,
  • Guixi Zheng2,
  • Ziyong Sun3,
  • Huijun Li3,
  • Peng Zhang4,
  • Wanli Liu5,
  • Ying Chen6,
  • Zhongying Zhang7,
  • Yi Xu8,
  • Yishan Huo8 and
  • Qishui Ou9
Journal of Ovarian Research20158:72

https://doi.org/10.1186/s13048-015-0201-z

Received: 5 August 2015

Accepted: 29 October 2015

Published: 9 November 2015

Abstract

Background

To determine reference intervals for serum levels of human epididymis protein 4 (HE4) in Chinese women.

Methods

In this multicenter (n = 9) study, 618 healthy women, 767 patients with non-malignant diseases, and 951 patients with malignant tumors were enrolled. Serum levels of HE4 were measured in all patients using electrochemiluminescence immunoassays. The influence of age, menopause, malignancy status and other characteristics on the levels of HE4 was evaluated using univariate and multivariate analyses. Confidence intervals (2.5–97.5 %) were determined in different populations.

Results

There were significant differences in HE4 levels among groups with different ages, menopause or malignancy status. Higher levels of HE4 were detected in elder compared to younger, post- compare to pre- menopause and malignant compared to benign subjects. Multivariate analysis showed that menopause and malignancy status, as well as smoking and pelvic masses were independent factors involved in serum HE4 levels. In pre-menopause stage, the reference ranges of HE4 level were 29.30–68.79, 28.12–1284.83 and 34.75–981.91 pmol/L in healthy, benign and malignant populations, respectively. In post-menopause stage, the reference ranges are 35.96–114.43, 39.11–2208.70 and 39.40–1678.13 pmol/L for those populations.

Conclusions

The present study has established the reference intervals of HE4 levels in pre- and post-menopause populations with different malignancy status.

Keywords

Human epididymis protein 4 Epithelial ovarian cancer Pelvic masses

Background

Ovarian cancer is one of the most common gynecologic cancers all over the world. The estimated annual incidence is 225,500 cases worldwide, and 140,200 patients die every year from the disease [1]. In China, the incidence of ovarian cancer has also increased in recent years, and it is now ranking the eighth most common cancer [2]. Despite the improvement of surgical techniques and development of a number of anti-tumor drugs and new therapies, the 5-year survival rate of late-stage ovarian cancer is only 30 % [3]. Therefore, early diagnosis of ovarian cancer is critical for prognosis and long-term survival. Unfortunately, due to the lack of specific symptoms at early stages, most patients are diagnosed only in late stages [4, 5].
Fig. 1

HE4 and CA125 distribution in EOC patients according to cancer stage. a and c, pre-menopause; b and d, post-menopause

The human epididymis protein 4 (HE4) (also called WFDC2) was originally identified as a small secreted protein that plays a role in sperm maturation in males [6], and it was found to be expressed in some ovarian cancers [7, 8]. Serum levels of HE4 have been shown to be useful for the diagnosis of ovarian cancer [911]. Not only may it be used to predict malignant status of pelvic mass, the HE4 level is also correlated with malignancy level and complexity of the disease [12]. In addition, it was shown to be correlated to surgery outcomes [13]. However, despite the existence of many methods for HE4 measurements, there is a lack of standardization and results cannot be compared between populations and studies. Previous studies have shown that age, fertility status, menopause, smoking, renal function, ethnicity, and detection method may affect serum HE4 levels [1418]. Therefore, reference intervals of serum HE4 levels need to be established in different populations stratified according to these factors. In addition, only limited data are available on HE4 levels in Han Chinese individuals living in China [17]. Therefore, there are large variations in HE4 reference ranges, causing uncertainty in clinical application.

Nevertheless, recent studies have described HE4 as a specific and useful biomarker for early diagnosis of epithelial ovarian cancer (EOC), which account for 90 % of all ovarian cancers [19]. In addition, incorporation of serum levels of HE4 and CA125 in the Risk of Ovarian Malignancy Algorithm (ROMA) [18] for clinical evaluation have resulted in improved EOC diagnosis specificity and sensitivity, and have helped distinguish malignant from benign pelvic masses [20, 21]. Other studies have equally demonstrated the importance of HE4 in predicting ovarian cancer recurrence [22, 23].

Therefore, the present multicenter study was undertaken to determine the factors influencing HE4 levels and the reference intervals of HE4 levels in a Chinese population.

Methods

Study participants

This multi-center (n = 9) study prospectively included healthy women and female patients (n = 2351) from October 2012 to February 2013. All participating sites received the approval of their ethics committee. The need for informed consent was waived by the committees since all specimens used in the present study were leftover samples.

The inclusion criteria for all individuals were: 1) Clinical records including age, menopause status, race, sex, smoking history, diagnosis of benign disease patients and pathological results were available; and 2) normal appearance of blood samples, with at least 0.5 ml being available. The exclusion criteria were: 1) patients <18 years old; 2) incomplete clinical data; 3) insufficient blood sample volumes (<0.5 ml); 4) blood stored or shipped at >0 °C; 5) samples submitted to >3 freeze/thaw cycles; or 6) blood sample with icteric, lipemic, hemolytic appearance or particles. Clinical diagnosis of the subjects included apparently healthy (618 specimens), non-malignant diseases (767 specimens) and malignant tumors (951 specimens including 287 EOC).

EOC diagnosis was confirmed by pathological analyses, and the EOC surgical staging was recorded.

HE4, CA125, E2, and Prog

All blood samples were taken at the time of primary diagnosis. At the time of blood sampling, no patient has been experienced any chemo- or radio- therapy. Blood specimens were centrifuged to obtain serum (at least 0.5 ml), and samples were frozen at −80 °C until analysis. HE4 and CA125 serum levels were determined in all samples using a Roche Elecsys Cobas 601 platform (Roche Diagnostics, USA) using specific assays and kits from for the detection of HE4 (Roche Diagnostics, Basel, Switzerland) according to the manufacturer’s instructions. The assay method used was electrochemiluminescence immunoassay (ECLIA) and the measurement range was 15.0–1500 pmol/L for HE4 All laboratories involved in this study passed the External Quality Assessment (EQA)/ISO 15189, as required by Chinese authorities. The same batch number reagents and controls were used in laboratories in all sites. All these laboratories passed the external quality assessment before the study.

Statistical analysis

Statistical analyses were performed using SPSS 18.0 (IBM, Armonk, NY, USA). Box-Cox regression was used for data transformation to obtain a normal distribution. Quantitative values are reported as N, median (range). Qualitative variables were described as numbers. One way ANOVA and Bonferroni post hoc test were used for comparisons. Reference intervals were determined by selecting the 2.5 and 97.5 percentiles. Multivariate linear regression analysis was used to evaluate correlations between different factors with HE4 levels. Differences were considered statistically significant at P < 0.05.

Results

Study population

A total of 2351 subjects were enrolled in the study including 618 healthy volunteers, 287 patients with epithelial ovarian cancer according to Federation International of Gynecology and Obstetrics (FIGO) staging and 1446 patients with various benign diseases and other cancers. The medium age was 49 (range 18–95) years. There were 1213 subjects in pre-menopause, 1137 post-menopause and 1 with unknown status (Table 1).
Table 1

Characteristics of the study population

Parameter

n (%)

Menopausal

 

 Pre-menopause

1213 (51.6)

 Post-menopause

1137 (48.4)

 Unknown

1

Healthy

618 (26.3)

Benign disease

767 (32.6)

 Benign gynecologic tumor

348

 Other gynecological disease

70

 Pregnant

108

 Congestive heart failure

43

 Renal failure

74

 Other benign diseases

124

Malignant disease

951 (40.5)

 Epithelial ovarian cancer (EOC)

287

  Stage I

33

  Stage II

37

  Stage III

121

  Stage IV

35

  Unknown

61

 Endometrial cancer

136

 Breast cancer

178

 Gastrointestinal cancer

139

 Lung cancer

145

 Bladder cancer

66

Mixed benign and malignant disease

15 (0.6)

Total

2351

Age median (range)

49 (18–95)

In the analysis of HE4 levels, 15 samples with combined benign and malignant diseases, 1 sample with unknown menopause status, and 4 samples with unspecified out-of-upper-limit HE4 levels were excluded, resulting in 2331 samples included in the final analysis. The numbers of samples included and excluded in different sitess were listed in Additional file 1: Table S1. To gain a rough estimate of HE4 levels in the general population, the reference ranges (95 % CI) of HE4 levels in the healthy population in this study were evaluated in different age groups as well as in pre- and post- menopause subjects (Table 2).
Table 2

HE4 reference range in healthy populations according to age or menopause status

 

Number

Value (mean ± SD)

Reference range (2.5–97.5 %)

Ages*

   

<40

201

45.85 ± 10.72

29.25–68.50

40–49

102

47.80 ± 9.73

32.11–68.96

50–59

104

54,11 ± 14.30

33.04–88.67

60–69

108

59.91 ± 14.33

34.72–92.35

≥70

103

77.57 ± 23.20

45.18–132.00

Pre-menopause

308

46.61 ± 10.70

29.25–68.96

Post-menopause

310

63.94 ± 20.21

34.72–114.90

Overall

618

55.30 ± 18.35

31.82–105.10

*A statistical significant difference in HE4 was found between each age group (p < 0.0001) except between <40 and 40–49

Factors that influence HE4 levels

It has been previously noticed that HE4 level in individuals could be affected by various factors including age, menopause and diseases [1418]. To determine which factors could interfere with HE4 level, study subjects were grouped based on age, menopause, and disease. As shown in Table 3, significant differences in HE4 levels were detected in patients grouped in each category. Aging, menopause, malignant diseases and increased staging of ovarian cancer seemed all result in increased levels of HE4. These results indicate that multiple interfering factors have to be considered to establish a reference interval of HE4 level.
Table 3

Influences of age, menopause or malignancy on HE levels

Parameter

Number

HE4 Value

P

Median (range)

Age

  

<0.001

 <40

628

47.275 (15–2982)

 

 40–49

544

51.01 (24.07–4322)

 

 50–59

520

59.47 (26.08–5234)

 

 60–69

371

66.63 (23.3–3844)

 

 ≥70

268

84.33 (24.22–2276)

 

Menopause

  

<0.001

 Pre-menopause

1206

48.81 (15–4322)

 

 Post-menopause

1125

68.46 (23.3–5234)

 

Malignancy status

  

<0.001

 Healthy

618

51.09 (23.3–166)

 

 Benign

765

51.92 (15–5234)

 

 Malignant

948

67.935 (26.08–4603)

 

Overall

2331

56.51 (15–5234)

 
To confirm the interfering factors of HE4 levels in individual, multivariate linear regression analyses were used to identify the correlations between different characteristics and HE4 levels. As shown in Table 4, when only age, menopause and malignancy status were considered, menopause and malignancy status, but not age, were independently associated with HE4 levels. When pregnancy status, smoking, and existence pelvic masses were added into the analysis, menopause and malignancy status were still independently associated with HE4 levels. Smoking and pelvic masses were also significantly associated with HE4 levels. Age seemed not to be an independently associated factor.
Table 4

Multivariate analysis of independent correlated factors of HE4 level

Parameter

Coefficient

P

Model 1

  

Age

0.691

0.432

Menopause

65.889

0.014

Malignancy status

64.385

<0.001

Model 2

  

Menopause

90.199

0.001

Smoking

212.286

0.006

Pelvic masses

68.517

<0.001

Malignancy status

53.140

<0.001

Model 1: age, menopause and malignancy status were included. Model 2: age, menopause, malignancy status, pregnancy, smoking, and pelvic masses were included. The associations with HE4 levels were analyzed using multivariate linear analysis using the enter regression method

HE4 reference range in different populations

Results indicated that the presence of an ovarian tumor and menopause status, but not age, had to be considered when determining whether HE4 levels are abnormal. The post-menopausal population generally had higher HE4 levels compared with pre-menopausal individuals. The presence of a malignant tumor, mostly ovarian cancer, could further increase HE4 levels. The detailed reference intervals of HE4 levels in healthy, individuals with benign tumors or malignant tumors, for pre- and post-menopause populations, are listed in Table 5. In pre-menopause stage, the reference ranges of HE4 level were 29.30–68.79, 28.12–1284.83 and 34.75–981.91 pmol/L in healthy, benign and malignant populations, respectively. In post-menopause stage, the reference ranges are 35.96–114.43, 39.11–2208.70 and 39.40–1678.13 pmol/L for those populations. In addition, HE4 and CA125 distribution in patients of different EOC stages also showed significant differences (Fig. 1).
Table 5

Reference ranges of HE4 in different populations

Populations

Reference range of HE4

Pre-menopause

Healthy

29.30–68.79

Benign

28.12–1284.83

Malignant

34.75–981.91

Post-menopause

Healthy

35.96–114.43

Benign

39.11–2208.70

Malignant

39.40–1678.13

Discussion

As mentioned previously, ovarian cancer at early stages can be effectively treated with surgery with significantly higher 5-year survival rate [3]. However, most ovarian cancers are diagnosed in their late stages and this is also one of the reasons why the acceptance of laparoscopic surgeries for ovarian cancer is much slower than that for other malignant female reproductive cancers [24]. Ghezzi et al. [25] and Bae et al. [26] described that minimally invasive surgeries, such as laparoscopic staging or restaging of early stage ovarian cancer are as safe and effective as open abdominal surgery. A systemic review also demonstrated that patients undergoing laparoscopic surgeries had lower blood loss, shorter hospital stay period and shorter time interval between surgery and chemotherapy compared with open abdominal surgery [27]. Therefore, diagnosis of the disease in early stages plays a critical role in the timely treatment and will bring more benefits for the patients. As a correlated biomarker with ovarian disease, HE4 may facilitate to optimize the early diagnosis of ovarian cancer. To the best of our knowledge, this is the first prospective multicenter study examining age-related reference ranges of serum HE4 levels in a Chinese population. The 2.5–97.5 % cut-offs were determined in different patient subpopulation. There were significant differences in HE4 levels among groups with different ages, menopause or malignancy status. Multivariate analysis showed that menopause and malignancy status, as well as smoking and pelvic masses were independent factors involved in serum HE4 levels.

Different studies indicated different effects of patients’ characteristics on HE4 levels. Ferraro et al. [14] have shown that the menopausal status was associated with HE4 levels, as well as smoking and renal function. Speeckaert et al. [11] have shown that menopause was associated with HE4 levels. A meta-analysis supported the previous point of view and also showed that the detection method was associated with HE4 variations as well [16]. A study has shown that longitudinal measurement of HE4 levels might be better than cross-sectional ones [28]. but the applicability of this approach in the clinical setting might be more difficult. A study in multiple Asian ethnicities revealed that age was associated with HE4 levels, as well as ethnicity (Malays vs. Indians and Chinese) [17]. Moore et al. [15] have shown that age, menopausal status and pregnancy were associated with HE4 levels. Taken together, these studies suggest that there are variations in the factors influencing HE4 levels among different populations. These differences might be population-specific, or may be the result of the small sample size observed in some studies. Further studies focusing on specific populations should determine the factors influencing HE4 levels before generalizing to other populations. In the present study, menopause, malignancy status, smoking, and pelvic masses were independent factors associated with serum HE4 levels.

A recent meta-analysis revealed that the capacity of HE4 in identifying malignant from benign lesions was high [16]. Beside the cancer itself, the histological type and cancer stage are associated with HE4 levels as well [11]. HE4 levels in EOC patients in this study were significantly higher than the subjects with benign diseases. Apparently the diagnostic value of HE4 level would be only significant at the early disease stages. Our data showed that the HE4 levels in stage I/II patients were significantly higher than that in subjects with benign ovarian disease, further indicating the value of HE4 as an early diagnosis marker. A study has shown that HE4 levels were better than CA125 levels for detecting ovarian cancer [29], which is supported by a meta-analysis [30]. A recent study revealed that the combination of HE4 levels with pelvis ultrasound achieved the best sensitivity for detecting ovarian cancers among different algorithms tested [31]. Further study is necessary to determine if the combination of HE4 measurements with other diagnostic modalities could promote the detection of ovarian cancer. Algorithms could be designed for the rapid screening of asymptomatic women.

The present study suggested that while using HE4 level as a potential indicator of ovarian cancer, other factors for each individual such as menopause, but not age, must be considered. Reference ranges need to be established after considering those interfering factors. The strength of the present study is that it had a relatively large sample size and samples were from multiple centers. However, there was also a limitation due to the variety of interfering factors, and the unavailability of some factors in a retrospective setting. Further study with larger sample size is needed to establish reliable reference ranges.

Conclusion

In conclusion, the present study has established the reference intervals of HE4 levels in pre- and post- menopause populations with different malignancy status.

Notes

Abbreviations

HE4: 

Human epididymis protein 4

EOC: 

Epithelial ovarian cancer

ROMA: 

Risk of ovarian malignancy algorithm

ECLIA: 

Electrochemiluminescence immunoassay

EQA: 

External quality assessment

ECLIA: 

Electrochemiluminescence immunoassay

Declarations

Acknowledgements

ROCHE diagnostic sponsored the research reagents. This work was supported by the National High Technology Research and Development Program 863 (2011AA02A111) and The National Natural Science Foundation of China (81071413; 30772493).

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Clinical Biochemistry, Chinese PLA General Hospital
(2)
Department of Clinical Laboratory, Qilu Hospital of Shandong University
(3)
Laboratory Medicine Department, Tongji Hospital, Tongji Medical College of HUST
(4)
Department of Clinical Laboratory, Tianjin Medical University Cancer Institute & Hospital
(5)
Department of Clinical Laboratory, Sun Yat-Sen University Cancer Center
(6)
Department of Clinical Laboratory, Fudan University Shanghai Cancer Center
(7)
Department of Clinical Laboratory, Zhongshan Hospital Xiamen University
(8)
Clinical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University
(9)
Department of Laboratory Medicine, The First Affiliated Hospital of Fujian Medical University

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© Tian et al. 2015

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