This study has been designed with the aim of assessing the impact of six months of treatment with four hormonal contraceptives using different routes of administration (oral, transdermal and vaginal) on the plasma levels of cholesterol, triglycerides, HDL cholesterol and LDL cholesterol.
Study design
This is an observational, prospective, randomised and concurrent study amongst women of childbearing age (18-45 years), under normal clinical practice conditions, who attend a family planning appointment to request a hormonal contraceptive and do not meet any of the study's exclusion criteria and have no contraindications for the use of hormonal contraceptive methods.
Materials and methods
324 women were included using a group randomisation system with the following distribution: 64 were randomised to the transdermal Norelgestromin group, 61 to the transvaginal-release Etonogestrel group, 67 to the oral Chlormadinone group, 69 to the oral Drospirenone group and 63 to a control group in which the subjects were not given any type of treatment. Plasma levels of cholesterol, triglycerides, HDL cholesterol and LDL cholesterol were determined before treatment and six months after taking the hormone steroid treatment, except in the case of the control group which was not give any medication.
Results
A statistically significant reduction of LDL cholesterol was found in the treatment group that received oral Chlormadinone and in the control group. On the contrary, this value increased in the other treatment groups, although this was not of statistical significance.
Coagulation parameters; Hormonal contraceptives; Platelet; Venous tromboembolism
The association of Hormonal Contraceptives (HC) and increased risk of cardiovascular disease and of Venous Thromboembolism (VTE) has been demonstrated in different studies [1,2], with evidence of a direct relation between this risk and the dose of the oestrogen component in the formulation [3,4].
In this respect, there has been a great emphasis in the past decades on the influence of plasma lipoproteins as a cardiovascular risk factor, to such an extent that any abnormal lipid profile was associated with increased cardiovascular risk.
It is widely accepted that the oestrogen component has a positive effect on the lipid profile, and thus, the higher the oestrogen dose in the preparation, higher is the positive effect on lipoproteins [5-8] (Figure 1). The evolution of contraceptives has tended to reduce the oestrogen/progestogen ratio, which has been counteracted by a reduction in the progestogen dose, leading to lower androgenicity. Preparations containing second-generation progestogens have a more negative effect on the lipid profile in relation to HDL levels, in comparison with those that contain third-generation progestogens. This difference is reduced when the progestogen and accompanying oestrogen doses are lowered (Table 1). The untoward effects of progestogen lead to a rise in LDL-cholesterol and apoprotein B, and a fall in HDL cholesterol and apoprotein A, all of which leads in turn to an atherogenic profile.
Figure 1: Influence of different CHCs on the lipid profile (*p<0.05).
|
VLDL |
TG |
LDL |
HDL |
Apoprotein A |
High-dose oestrogens |
ááá |
ááá |
|
áá |
áá |
Low-dose oestrogens |
áá |
áá |
|
á |
á |
2nd generation progestogens |
â |
â |
á |
á/-- |
â |
3rd generation progestogens |
-- |
-- |
á/-- |
á/-- |
â |
Table 1: Effect of steroids on the lipid profile [5-8].
In this respect it has been demonstrated that Norgestimate, Desogestrel and Gestodene increase HDL-C (lipoprotein protectors) but it is not known whether these biochemical changes are important from a clinical point of view [9-11]. Engel et al. [12], performed coronary angiography in women who had suffered a myocardial infarction and found that 36% of the women who had used oral contraceptives had diffuse atherosclerosis, while 79% of those who did not use oral contraceptives also had it, concluding that in women with previous myocardial infarction who were taking oral contraceptives, the infarction was not of atherosclerotic origin, but rather of thrombotic origin. This viewpoint supports the hypothesis put forward by Lobo et al. [13], that micro-dose oral contraceptives, including last-generation progestogens, afford heart protection.
Low-dose contraceptives have no effect on total cholesterol and its fractions, despite reducing the progestogen/oestrogen ratio, since the type of progestogen has been modified (it is less androgenic) and the dose has also been reduced [5,14].
In this study we used low-dose HC, varying the progestogen component and route of administration as authorised in recent years on the Spanish market. Thus, the following combinations of HC were given for 6 months:
Combined HC containing 2mg of Chlormadinone Acetate (CMA) and 0.030mg of EE.
Combined HC containing 3mg of Drospirenone (DRSP) and 0.030mg of EE.
Study design
The study scrupulously followed the recommendations of the Declaration of Helsinki (Hong Kong, 1989), European Good Clinical Practice Guides, and all participants were duly informed in writing, and provided their consent before commencing the study.
The women were randomised into 5 groups. 4 of these groups were treatment groups: NGNM group (TRS, 0.120mg NGMN/ 0.02mg EE); ENG group (VRS, 0.120 ENG and 0.015mg EE); CMA group (oral, 2mg CMA/ 0.030mg EE); DRSP group (oral, 3mg DRSP/ 0.030mg EE); and a control group (which was not given any CHC).
The contraceptive was administered on the first day following menstruation, and each patient was informed of the correct method of administering each CHC.
The study was conducted in the gynaecology clinic at the Vicalvaro Municipal Health Centre in Madrid (Spain) between October 2008 and February 2009.
The study inclusion criteria were: Women of childbearing age (18-45 years), without any contraindications for having hormonal contraceptives prescribed, who were not planning to become pregnant during the duration of the study (6 months) and who attended the gynaecology clinic requesting a hormonal contraceptive method in the case of the patients in the treatment groups, or for a routine check-up, not having used any hormonal contraceptive method for 6 months prior to commencing the study (control group).
The study exclusion criteria included contraindicated use of CHC, age under 18 or over 45 years old, women who might want to become pregnant within 8 months, patients who did not agree to undergo clinical and laboratory tests at the intervals defined in the study protocol, and women who referred to poor compliance with the established dose regime in their contraceptive history.
The study was planned to last 6 months and entailed 2 visits: A baseline visit and a final visit.
The following procedures were scheduled at the baseline visit: medical history, cervical-vaginal cytology, transvaginal ultrasound, verification of normal laboratory test values with regard to lipid profile and blood biochemistry, recording of blood pressure, height and weight, and calculation of Body Mass Index (BMI).
After 6 months of treatment, a second visit was scheduled in order to assess the following parameters: treatment follow-up, medical history, transvaginal ultrasound, evolution of laboratory values, recording of blood pressure, height and weight, calculation of BMI, compliance with medication regime, as well as an assessment of any adverse events derived from the use of the CHC.
Laboratory tests
Blood samples were obtained through venipuncture. Approximately 12ml of blood were taken and distributed as follows: 3ml in a glass test tube containing 0.05ml of 8% EDTA for haematology; 4ml in a glass test tube without anticoagulant for biochemistry. A Coulter autoanalyser was used for the blood count and a Siemens ADVIA® 1650 Chemistry System autoanalyser was used for biochemistry.
Lyphochek® and Assayed Chemistry Control (Biorad) were used as reference controls for the different laboratory values.
The specific laboratory values that were determined for the lipid profile parameters were: Total cholesterol (g/dL); HDL cholesterol (g/dL); LDL cholesterol (g/dL), triglycerides (g/dL).
We also calculated the atherogenicity index in each subject in the treatment groups and in the control group.
Statistical analysis
We assessed the influence of the four OHC on the lipid parameters. All parameters have been summarised, with respective descriptive statistics, mean and standard deviation.
We used Student's t-test to compare the biochemistry parameters. We used SPSS v.15.0 statistical package for the statistical analysis of data.
Statistical significance was considered as a value of p<0.05.
Distribution of study subjects
A total of 324 women of childbearing age were included. They were randomised to the following groups: EE/NGMN (n=64); EE/ENG (n=62); EE/CMA (n=68); EE/DRSP (n=70); Control (n=64).
During the 6 months that the study lasted, there were no drop-outs for adverse effects, protocol breaches or non-compliance with inclusion criteria.
Baseline characteristics
Baseline demographic data included age, weight, height, BMI and age at first menstruation (menarche) (Table 2). It can be observed that there were no differences between the different study groups.
|
EE/NGMN (n=62) |
EE/ENG (n=60) |
EE/CMA (n=68) |
EE/DRSP (n=70) |
Control (n=64) |
Age (years) |
28±6.15 |
28.77±13.18 |
29.79±7.23 |
28.51±6.20 |
33.66±5.86 |
Weight (kg) |
62.38±13.18 |
60.14±11.93 |
60.81±8.53 |
61.36±8.27 |
64.00±11.79 |
Height (cm) |
181.66±8.14 |
131.13±22.68 |
161.44±6.64 |
162.26±6.04 |
161.63±6.16 |
BMI: |
23.31±3.78 |
22.68±3.92 |
23.03±2.72 |
23.14±3.17 |
24.13±3.96 |
Menarche (years) |
12.34±1.3 |
12.77±1.64 |
12.26±1.5 |
12.66±1.02 |
12.66±1.4 |
Table 2: Baseline demographic data.
Lipid parameters
The data for the lipid parameters assessed in this study are shown in table 3.
|
|
|
Mean |
Min |
Max |
Standard Dev. |
p |
EE/NGMN (n=62) |
Tot chol |
Start |
183.74 |
99 |
250 |
39.62 |
0.00055 |
|
|
6 cycles |
195.29 |
118 |
275 |
34.68 |
|
|
HDL-Chol |
Start |
59.61 |
40 |
81 |
10.10 |
0.00000 |
|
|
6 cycles |
67.35 |
46 |
96 |
11.65 |
|
|
LDL-Chol |
Start |
112.68 |
37 |
200 |
35.05 |
0.88517 |
|
|
6 cycles |
113.06 |
37 |
204 |
29.88 |
|
|
TG |
Start |
82.26 |
25 |
159 |
32.47 |
0.76883 |
|
|
6 cycles |
99.58 |
33 |
211 |
47.17 |
|
EE/ENG (n=60) |
Tot chol |
Start |
179.97 |
116 |
252 |
32.05 |
0.25729 |
|
|
6 cycles |
185.23 |
89 |
260 |
44.28 |
|
|
HDL-Chol |
Start |
62.84 |
42 |
105 |
13.38 |
0.40696 |
|
|
6 cycles |
64.26 |
44 |
103 |
17.40 |
|
|
LDL-Chol |
Start |
104.77 |
55 |
174 |
24.27 |
0.95225 |
|
|
6 cycles |
104.97 |
45 |
184 |
33.37 |
|
|
TG |
Start |
77.90 |
38 |
170 |
31.57 |
0.07470 |
|
|
6 cycles |
85.39 |
56 |
180 |
35.77 |
|
EE/CMA (n=68) |
Tot chol |
Start |
177.79 |
131 |
265 |
32.34 |
0.01784 |
|
|
6 cycles |
185.56 |
116 |
259 |
35.16 |
|
|
HDL-Chol |
Start |
62.09 |
42 |
91 |
11.19 |
0.00000 |
|
|
6 cycles |
70.41 |
36 |
112 |
17.03 |
|
|
LDL-Chol |
Start |
103.32 |
59 |
158 |
28.51 |
0.03868 |
|
|
6 cycles |
97.12 |
39 |
150 |
28.51 |
|
|
TG |
Start |
78.06 |
40 |
200 |
34.06 |
0.00000 |
|
|
6 cycles |
98.85 |
40 |
219 |
45.01 |
|
EE/DRSP (n=70) |
Tot chol |
Start |
174.97 |
106 |
238 |
33.49 |
0.10900 |
|
|
6 cycles |
182.63 |
115 |
262 |
44.12 |
|
|
HDL-Chol |
Start |
63.66 |
34 |
101 |
19.07 |
0.00011 |
|
|
6 cycles |
70.06 |
41 |
112 |
21.74 |
|
|
LDL-Chol |
Start |
98.40 |
56 |
143 |
22.42 |
0.87503 |
|
|
6 cycles |
98.94 |
48 |
187 |
30.47 |
|
|
TG |
Start |
77.54 |
29 |
206 |
35.65 |
0.01645 |
|
|
6 cycles |
86.03 |
37 |
220 |
40.05 |
|
Control (n=64) |
Tot chol |
Start |
182.78 |
138 |
228 |
24.13 |
0.08242 |
|
|
6 cycles |
178.03 |
140 |
214 |
21.06 |
|
|
HDL-Chol |
Start |
59.97 |
36 |
79 |
9.75 |
0.66525 |
|
|
6 cycles |
59.50 |
37 |
80 |
9.19 |
|
|
LDL-Chol |
Start |
110.03 |
71 |
165 |
22.37 |
0.00334 |
|
|
6 cycles |
103.25 |
58 |
140 |
17.79 |
|
|
TG |
Start |
83.72 |
40 |
183 |
35.24 |
0.84350 |
|
|
6 cycles |
84.72 |
31 |
199 |
40.90 |
|
Table 3: The effect of study treatment on lipid and lipoprotein profiles.
The group given EE/NGMN through TRS (transdermal release system) underwent a mean increase of 11.55mg/dl in total cholesterol. Their HDL cholesterol values, in turn, underwent a mean increase of 7.74mg/dl. LDL cholesterol levels remained almost unchanged, unlike triglyceride levels, which underwent a mean increase of 17.32mg/dl at the end of the study period.
On the other hand, the EE/ENG treatment group, administered through VRS (vaginal release system) also showed a small increase in total cholesterol values, of 5.26mg/dl. HDL and LDL cholesterol values at the end of the study hardly changed at all in comparison with the baseline values. A slight upward trend was observed in the mean triglyceride value, of 7.49mg/dl.
With regard to the women included in the oral EE/CMA treatment group, a small increase was found in total cholesterol values, of 7.77mg/dl. HDL cholesterol values underwent a mean increase of 8.32mg/dl. There was a noteworthy fall in mean LDL cholesterol values from the start to the end of the study, of 6.2mg/dl. On the contrary, triglyceride values increased 20.79mg/dl.
When analysing the group of women who were given the oral preparation containing ethinyl estradiol and drospirenone, they were found to have an increase in total cholesterol of 7.66mg/dl. The HDL cholesterol level increased 6.4mg/dl at the end of the six-month treatment period. The end LDL cholesterol values were similar to those obtained in the first test. Triglyceride values rose minimally, by 8.49mg/dl.
Amongst the women who were not subjected to exogenous steroid hormone action (control group), there was a minimal fall in total cholesterol levels of 4.75mg/dl. The most notable finding in the second test results in this group of women was that the HDL cholesterol and triglyceride values remained unaltered in comparison with the baseline tests. However, the LDL cholesterol values decreased by 6.78mg/dl in comparison with the initial values, even though these women were not given any treatment.
Contraceptive measures are not a modern practice. Efforts to limit reproduction are as ancient as sexual relations themselves. Contraceptives are one of the most commonly-used synthetic substances worldwide in preventing pregnancy. They are not risk free, however, and appropriate medical assessment is required before starting to take them.
Combined hormonal contraceptives are composed of two substances, regardless of the route of administration that is chosen. One is a synthetic (not natural) oestrogen. The commonest is ethinyl estradiol and, less frequently, mestranol. The metabolism of this compound varies from person to person and in different populations. At the same dose, positive and negative effects can be highly variable [15-17]. During the course of the broad experience that has been gained with these compounds, great importance has been given to the dose of the oestrogen component, and its relationship with undesired side effects, such as thromboembolism and circulatory problems [17-19].
The second component is gestagen or progestogen. This compound has undergone great changes in the last 20 years, because new products have been developed with lower doses, leading to a significant reduction in side effects, such as androgenic manifestations and modifications in the lipid profile [20-23].
Older contraceptives had a high dose of progestogens and were associated with adverse changes in the lipid profile [7,24]: Decreased HDL-C and increased LDL-C, creating atherogenic conditions [25]. Oestrogens in themselves cause an increase in HDL-C and lower LDL-C, and therefore the lipid profile depends on the balance between the effects of oestrogen and progestogen. It is very likely that the ethinyl estradiol in oral contraceptives directly protects coronary arteries from atherogenesis, inhibiting LDL-C in blood vessel walls [25]. It is believed that third-generation progestogens have a neutral action on lipids and therefore, combined oral contraceptives containing progestogens would have a positive effect on lipid changes [25].
In this study, the products that we analysed had a similar quantity of EE, belonging to the so-called low-dose CHC group, and we varied the progestogen dose and route of administration. A correct balance between the EE and progestogen content in the preparation is very important in order to minimise the impact on the lipid profile [26].
Randomised clinical trials that are available at present have been conducted on small sample groups, and do not compare risks between women taking OHC and those who do not, but between women taking different types of OC. Some studies have found statistically significant increases in different biochemistry parameters, but within normal values.
Evidences obtained from first-generation OCs cannot be extrapolated to third-generation preparations that are used nowadays, with ethinyl estradiol doses that are six times lower and combined with radically different progestogens [19,27]. In general, the actions of synthetic steroids are very different when oestrogens or progestogens are used on their own or in combination. Ethinyl estradiol causes an increase in HDL, a reduction in LDL plasma levels, and increased VLDL, and TGL to a lesser extent [28-30]. In general, progestogens reduce VLDL and HDL fractions in plasma and increase LDLs [28-30].
However, there are very significant differences between the different types of progestogens. The strongest atherogenic action is found in 19-nortestosterone derivatives (norethisterone and lynestrenol). On the contrary, the least impact is presented by hydroxyprogesterone derivatives (cyproterone acetate) and third-generation progestogens [20-23]. As a consequence, the global effect of OCs depends, theoretically, on the combination of the EE dose and the type and dose of the progestogen.
Oestrogens act on HDLs by means of two mechanisms: by suppressing hepatic lipase activity, leading to a reduction in HDL2 conversion into HDL3, and by increasing apoprotein A synthesis [30-32]. On the contrary, androgenic progestogens stimulate hepatic lipase activity. These mechanisms explain why an increase in oestrogen-induced increase in HDLs can be counteracted by the progestogenic component [33,34]. That is why OCs in current use contain third-generation progestogens, offering a clearly positive balance in HDL metabolism because they do not neutralise the beneficial effects of EE.
The mechanism by which androgenic progestogens increase LDL values is still not clear. Theoretically, the way these progestogens stimulate hepatic lipase activity should facilitate VLDL conversion into LDL [33,34]. This mechanism, together with the EE-induced stimulation in VLDL production, could result in increased LDL values. Contraceptive preparations containing third-generation progestogens has a lesser impact on the lipid profile.
OHC action on VLDLs and TGs represent one of the most important aspects in the way OCs influence lipid metabolism. The majority of studies have found an increase in TG and VLDL plasma values in eminently oestrogenic preparations, as a result of the increased VLDL product and reduced clearance rate induced by EE [33]. OHCs containing 19-nortestosterone-derivative progestogens have a palliative action on this effect.
Recent studies have demonstrated with sufficient evidence that OCs do not significantly increase lipoprotein A plasma values, and elevated lipoprotein A is clearly associated with ischaemic diseases.
In this study, after analysing total cholesterol values, we found a minimal increase in all groups except the control group, which showed a slight, insignificant fall [5,14] (Figure 1). This minimum impact on total cholesterol levels does not have a clinical repercussion in healthy women, and it confirms the results obtained in similar studies for the following combinations: 0.120mg NGMN/ 0.02mg EE in TRS format [35], 0.120 ENG and 0.015mg EE in VRS [36,37], 2mg CMA/ 0.030mg EE orally [38] and with the oral combination of 3mg DRSP/ 0,030mg EE [39,40].
In our study the biggest increase in total cholesterol was found in the Drospirenone and Norelgestromin groups, with a common increase for both of 11.5mg/dl. The smallest increase was found in the vaginal ring group, with a mean of 5.5mg/dl. These values are of statistical significance (p<0.05), but will not be clinically relevant in healthy women. Furthermore, the minimum increases in cholesterol levels match previously published studies on this type of CHC [35,39,40].
With regard to the HDL figures, a small increase was observed in all treatment groups, and the highest values were found in those who took Drospirenone and Norelgestromin, with a figure of 7mg/dl (Figure 1).
In relation to repercussion in LDL cholesterol values, changes were minimal in all treatment groups. The biggest reduction was found in women taking Chlormadinone, with a value of 6.21mg/dl.
The impact on triglycerides shows an increase in all treatment groups. The maximum value was found in the Chlormadinone group, with an increase of 20.7mg/dl, and the minimum value was found in the Etonogestrel group, with a value of 9.8mg/dl. In all study compounds it was confirmed that CHCs have a negative impact on triglyceride values, regardless of their route of administration [35-40].
Although it is suggested that the low-dose oral contraceptives that are used at present, combined with third-generation progestogens, have a clearly positive balance because they do not neutralise the beneficial action of ethinyl estradiol on high density lipoproteins, it is also acknowledged that androgenic progestogens stimulate the activity of hepatic lipase, leading to reduced HDL and decreasing apoprotein A synthesis. These mechanisms would explain why an ethinyl estradiol-induced increase in HDL could be counteracted by the progestogenic component, which also causes an increase in low density lipoproteins [41].
These modifications in the lipid profile have a minimal or nil clinical impact, although it should be remembered these treatments are potentially prescribed over a long period of time.
In view of the results obtained from this study and previous studies, we can recommend that in a healthy population there is little evidence to support the need for systematic determination, either in new users or in women who are already taking them. On the contrary, it is essential to assess this in women with established cardiovascular disease or with multiple risk factors (arterial hypertension, obesity, smokers, family history of premature heart disease).
On the contrary, combined hormonal contraceptives are contraindicated in women with ischaemic heart disease and hyperlipidaemia, even if the latter is controlled with medication. They are relatively contraindicated in women with isolated hyperlipidaemia without other associated cardiovascular risk factors.
OCs with third-generation progestogens are not recommended if there is hypertriglyceridaemia, since they lead to increased triglyceride plasma levels. It appears that hypertriglyceridaemia is related to an increase in prothrombotic factors and a reduction in fibrinolysis.
In our study, the oral combination EE/CMA was the CHC that causes the least impact on the lipid profile.
Citation: Beltran DA, Crespo AB, Valle SG, Iglesias AG (2020) Effect of Four Hormonal Contraceptives on Lipid Profile Under Real Conditions of Use After 6 Months of Treatment. J Food Sci Nutr 6: 065.
Copyright: © 2020 Crespo AB, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.