Findings

Background

Endometriosis is an estrogen dependent chronic inflammatory disease characterized by the survival of endometrial tissue outside the uterine cavity [1]. Endometriosis which affects an estimated 6-10% of women of the reproductive age group, is a considerable burden to affected women, their families and healthcare systems [2].

Among the etiological factors that promote the survival of ectopic tissue, estrogenic compounds that promote protracted continuation these tissues are gaining prominence supported by persuasive evidence from in vitro, in vivo and human studies [3].

Compelling molecular [4], in vitro[5] and in vivo[6] evidence for the ability of metal ions to activate the estrogen receptor [7] has defined a group of xenoestrogens termed metalloestrogens [8]. While evidence for the purported estrogenicity of cadmium are in plenty, estrogenic properties of other metals such as nickel have also been demonstrated by some research groups [9].

In vivo experiments by Krugner-Higby et al. [10] have demonstrated that the occurrence of endometriosis was higher in six female rhesus monkeys exposed to a daily intake of 5 to 10 mg/Kg of lead as compared to a control group (n= 4) given lead-free water over a period of 19 years, but the difference was not statistically significant, probably due to the small sample size [10].

We have previously demonstrated the presence of cadmium, lead and nickel in ectopic endometrial tissue in a group of Sri Lankan women [11]. Heavy metals enter the human body either by ingestion or inhalation and are subsequently transferred to the vascular compartment (blood) [12]. Metals derived from the circulation get deposited in the tissues by various mechanisms [13]. We hypothesized the hematogenous route (blood) as a possible source of metals in the ectopic endometrial tissue.

The present study was conducted with the objective of exploring further the association between endometriosis and whole blood levels of cadmium, lead and nickel in the same group of women with endometriosis who were previously studied. We compared the whole blood levels of the cadmium, lead and nickel in women having endometriosis (in whom these metals were detected in ectopic endometrial tissue -cases) with the blood levels of same metals in women who had no evidence of endometriosis (controls).

Methods

This case control study was conducted among women of the reproductive age group, at the Professorial Gynecology Unit of the National Hospital, Colombo, Sri Lanka. Patients awaiting elective laparotomy or laparoscopy for diagnostic and/or treatment purposes were included. Those who were diagnosed visually as having endometriosis subsequent to laparotomy or laparoscopy were selected as cases (n=50). Apart from the ectopic endometrial tissue sample that was collected as described in the previous study [11], simultaneous venous blood sample was collected from each case. Women matched for age in whom endometriosis had been excluded by laparoscopy or laparotomy were recruited as controls (n=50). Indications for laparoscopy or laparotomy in controls were subfertility, dysmenorrhea, chronic pelvic pain or detection of an ovarian mass in ultrasound scan.

A sample of venous blood was collected from all participants during intravenous cannulation at the time of induction of anesthesia into polypropelene tubes containing ethylene diamine tetraacetic acid (EDTA). Pre-operatively, informed written consent was obtained from all the participants. All the blood samples were stored in a −20°C freezer until analysis.

Whole blood samples were digested using a protocol described previously [14] with some modifications. Briefly, matched blood of cases and controls were allowed to reach the room temperature. Then whole blood samples were transferred to pre-treated, acid washed glass beakers. The wet weight of each sample was determined using a chemical balance. Each sample was prepared in duplicate. All the blood samples were digested using 65% supra pure Nitric acid (HNO3, Merck, USA) while maintaining a uniform temperature. The final solution was made in 2mL of 5% HNO3 that was prepared by diluting the 65% supra pure HNO3 with double distilled deionized water.

The total-reflection X-ray fluorescence (TXRF) machine available at the Atomic Energy Authority (AEA) of Sri Lanka was utilized to measure metals apart from cadmium. TXRF is a multi element analysis technique [15] capable of detecting an array of elements at detection levels of picograms per liter (pg/L) [15]. An internal standard, Gallium, allows quantification of metals using the Axil software. However, the TXRF that was used had an inherent weakness in measuring cadmium since it had a Molybdenum x-ray tube. Therefore, we used atomic absorption spectroscopy (model GBC 933AA) together with a graphite furnace (model GBC GF 3000) available at the Institute of Fundamental Studies (IFS), Kandy, Sri Lanka to estimate cadmium levels as described elsewhere[16]. Both AEA and IFS [16] are national level apex institutions in Sri Lanka that have international certifications for trace element analysis where regular quality assurance programs are conducted.

Quality control and validation were performed using reference material supplied by the International Atomic Energy Authority (IAEA-A-13), Seronorm™ trace elements in whole blood levels 1 (MR 4210) and National Institute of Standards & Technology (NIST) Gaithersburg, USA water sample with trace elements (SRM 1643e). For 96% of the determinations, repeatability error did not exceed 10%. The detection limits for nickel, lead and cadmium in whole blood were as follows 0.05, 1.0, 0.01 μg/L. The precision for nickel, lead and cadmium in the range of the samples analyzed in this study was + 2, 3 and 6%, respectively.

SPSS version 13 for Windows was used for statistical analysis. Log transformation of metal levels was done and means were compared using t-test.

Ethical clearance was obtained from the Ethical Review Committees of the Faculty of Medical Sciences, University of Sri Jayewardenepura and the National Hospital of Sri Lanka.

Results and discussion

Mean (±SD) age in cases and controls were 33.0 (±5.4) and 32.7(±5.4) years respectively. Cases and controls were similar in body mass index while none of the women who participated in the study were current smokers. Other demographic, biological and dietary characteristics of this group of women with endometriosis have been described previously [17].

Cadmium, lead and nickel were detected in whole blood of all the participants. The whole blood nickel levels in cases were significantly higher compared to controls. Cases had lower whole blood cadmium levels and higher lead levels as compared to controls; however these differences were not statistically significant (Table 1).

Table 1 Levels of metalloestrogens in whole blood (μg/L) of cases and controls
Full size table

Environmental pollution has been identified as a potential cause for the increase in the prevalence of endometriosis following industrialization [18]. Heavy metals are gaining prominence as pollutants that could affect human health profoundly, especially in the face of escalating levels of environmental contamination [19]. Women are susceptible to heavy metal toxicity due to differences in kinetics, mode of action, susceptibility and exposure [20, 21].

The demonstration of higher levels of nickel in whole blood in women with endometriosis as compared to controls in our study is a novel finding. Hitherto, there is no published literature that has investigated the nexus between nickel and endometriosis. The whole blood nickel levels we are reporting are comparable to those reported from women in the general population in different countries [22, 23]. Thus the levels we have detected are essentially non toxic levels although cases had higher nickel levels which may have contributed towards the presence of nickel in ectopic endometrial tissue.

Nickel similar to other heavy metals, primarily enters the human body either by ingestion or inhalation [24]. In addition, nickel is a common metal found in accessories frequently used by women [20] and its absorption via intact or damaged skin has been demonstrated [25]. Martin et al. [26] assessed the estrogenic potency of metals using the 50% effective concentration (EC50) of different metals as determined from dose–response curves performed in MCF-7 cells transiently transfected with the luciferase reporter construct. They found that nickel had a relative potency of 1.0 compared to estradiol [26] implying that nickel is a potent metalloestrogen.

Humans studies that attempted to elicit the association between cadmium and lead and endometriosis have yielded conflicting results. In a population based study in the United States, high blood concentrations of cadmium were associated with endometriosis [27]; while a study done in Belgium reported similar levels of cadmium and lead in blood in both cases and controls [28]. Urinary cadmium concentrations were similar in cases with endometriosis and controls [28, 29]. The results of this study are in agreement with the previously published research apart from that of Jackson et al. In the study conducted by Jackson and co workers that probed the association between cadmium and endometriosis, a considerable number of women with endometriosis were smokers [27]. In contrast, in our cohort of women none were current smokers.

In conclusion in this group of women with endometriosis higher blood levels of nickel were observed. Whether nickel could be considered as an etiological factor in endometriosis remains inconclusive considering two factors, namely the small sample size evaluated in this study and the absence of a previous report of such a link. However based on the available scientific evidence for occupational and environmental exposure of women to metals including nickel, future research would prove to be invaluable in further exploring the association between nickel and endometriosis.