Effect of the Monthly Injectable Combined Contraceptives versus Oral Contraceptive Pills on Mood

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Korean J Fam Med. 2021;42(6):471-476

Publication date (electronic) : 2021 November 20

doi : https://doi.org/10.4082/kjfm.20.0106

Ghada M. Khafagy^1,, Hebatallah L. Shalaby², Nagwa E. Saad³, Marwa D. Hasan¹

¹Department of Family Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt

²Department of Family Medicine, Ministry of Health, Cairo, Egypt

³Department of Internal Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt

*Corresponding Author: Ghada M. Khafagy https://orcid.org/0000-0001-6941-7291 Tel: +20-01006393140, Fax: +20-023499141, E-mail: ghada.khafagy@kasralainy.edu.eg, ghadakhafajy@yahoo.com

Received 2020 May 11; Revised 2020 July 16; Accepted 2020 July 18.

Abstract

INTRODUCTION

Family planning can be used to delay pregnancy, especially in young mothers, thereby decreasing health-related problems and deaths in early childbearing. In addition, it can prevent high risk unintended pregnancies in older women [1]. For the last 50 years, daily combined oral contraceptive pills (COC) have been the favored short-acting hormonal contraceptives among most women. However, this system is an unsuitable or suboptimal choice for others [2]. Injectable contraception has been a popular contraceptive tool for several years. Currently, over 40 million women worldwide use injectable contraceptives to prevent pregnancy [3]. Combined injectable contraceptives (CIC) containing varying proportions of both estrogen and progestin were developed as a method of choice for women desiring the benefits of injectable contraception, while minimizing the side effects of progestin-only formulations. CIC have proven to be a highly effective and reversible method of birth control [4].

Although the use of combined hormonal contraception for women with mood disorders is not restricted and is considered to be safe [5], the main cause of discontinuation of the combined contraceptive methods is the mood-related side effects. The percentage of women who complained of depressive mood, irritability, and anxiety ranges from 4%–10%, and this problem can lead to lack of compliance, resulting in unintended pregnancies [6]. Therefore, mood monitoring and reporting of negative symptoms are advised, and women should consider alternative contraceptive methods accordingly, on an individual basis [5].

In 2020, the World Health Organization reported that women are more prone to depression than men, especially during the adolescence stage, which in turn leads to disabilities and increases the risk of suicide [7]; therefore, it is important to know if any association exists between depressive symptoms and widely used contraceptive methods [8]. On reviewing the literature, we noticed that there was a lack of data on this area; accordingly, we aimed to estimate the severity of adverse mood in combined contraceptive use.

METHODS

This prospective cohort study was conducted from April 2018 to February 2019 on 128 women aged between 18–45 years old who presented to outpatient clinics seeking medical advice for contraception in the Kom-Ashfeen Family Medicine Unit, El-Kalyubia district, Egypt.

Participants were enrolled between April and August 2018. Women known to have thromboembolic diseases, hypertension, breast cancer (current or prior), diabetes, migraine with aura, and/or known psychiatric illnesses were excluded. Breastfeeding mothers and mothers who had delivered within the prior 6 months were excluded.

After initial enrollment of 208 patients according to the selection criteria, the physicians counseled the patients regarding the different contraceptive options, providing the advantages, disadvantages, and reliability of each different method; as a result of counseling, the patients individually decided which method to use. A total of 148 patients who chose to start using combined monthly injectable, combined oral pills, or an intrauterine device (IUD) were invited to participate in the study; 20 refused and 128 accepted. Those who accepted were divided into three groups according to their choice, as follows:

Group A included 48 participants who received monthly CIC; progesterone estrogen for hormonal contraception. Each 1 mL ampule contained 50 mg norethisterone enanthate and 5 mg estradiol valerate in oily solution. Forty-four patients completed the study, while four patients were lost to follow-up.

Group B included 40 participants who received COCs; progestin-estrogen combination for oral contraception; the contraceptive pack contains 21 tablets each with 0.15 mg levonorgestrel and 0.03 mg Ethinyl estradiol. All patients in this group completed the study.

The control group, C, included 40 participants who used a copper T IUD, all of whom completed the study.

In the first visit, the medical history of all patients in the three groups was taken using the sheet of El-Gilany et al. [9], which surveyed sociodemographic data, medical, menstrual, and obstetric history. This was followed by a clinical examination. Patients were assessed for depressive symptoms in their intermenstrual phase using the validated Arabic form of the Patient Health Questionnaire-9 (PHQ-9) before the start of the contraceptive method and 6 months later [10]. The PHQ-9 is a validated tool that assists clinicians in diagnosing depression and monitoring treatment responses. The nine items of the PHQ-9 are based directly on the nine diagnostic criteria for major depressive disorder in the Diagnostic and Statistical Manual of Mental Disorders, 4th edition; its internal consistency is 0.89. A PHQ-9 score ≥10 has a sensitivity of 88% and a specificity of 88% for major depression. PHQ-9 scores of 5, 10, 15, and 20 represented mild, moderate, moderately severe, and severe depression, respectively [11,12].

RESULTS

Table 1 shows that there was no statistically significant difference between the three groups in terms of age and social class, ensuring homogeneity and matching of the three groups. Further, there was no statistically significant difference between the three studied groups in terms of the obstetric history (number of pregnancies (P=0.77), abortions (P=0.09), children (P=0.62), previous cesarean sections (P=0.49), normal labors (P=0.35), age of the oldest (P=0.93) and youngest son (P=0.98); and all participants’ deliveries were performed under medical supervision and passed safely without any post-partum complications.

Table 1.

Socio-demographic characteristics of the study subjects

The majority of the women in this study had regular menses, moderate in quantity, and there was no statistically significant difference between the three studied groups in terms of menstrual history (P=0.3), or the types of previously used contraceptive methods (P=0.51).

Table 2 shows that there were statistically significant differences between the three studied groups in terms of the PHQ-9 score after 6 months of follow-up (P<0.05), and the mean change in PHQ-9 score was higher in the combined injectable users, although this difference was not statistically significant compared to oral contraceptives (P=0.51). Table 3 shows that there were statistically significant differences between the pre- and post-results of groups A and B regarding PHQ-9 score after 6 months of follow-up (P<0.05). As shown in the boxplot graph in Figure 1, there were statistically significant differences between groups A and B in terms of the PHQ-9 score after 6 months of follow-up (P<0.05).

Table 2.

Comparison between the PHQ-9 score in the studied groups before the study and after 6 months of follow-up

Table 3.

Comparison between pre and post results of PHQ-9 within each of the three groups

Figure. 1.

Flow chart demonstrating the selection of study participants. CIC, combined injectable contraceptives; COC, combined oral contraceptives; IUD, intrauterine device.

Figure 2 shows that before the study, there were no statistically significant differences among the studied groups regarding PHQ-9 score categories. The largest percentage of participants had no depression; 77.3% of the women in group A (COC users), 75% of the women in group B (CIC users), and 87.5% of the women in group C (IUD users) did not have depression, while 22.7%, 22.5%, and 12.5% of women in groups A, B, and C had mild depression, respectively.

Figure. 2.

Comparison between the Patient Health Questionnaire-9 (PHQ-9) scores in the studied groups before the study and after 6 months of follow-up. The symbol ° indicates possible outliers and the symbol ★ indicates the most probable outliers.

Figure 3 shows that after 6 months of follow-up, 54.5% of the women in group A, 50% of the women in group B, and 27% of the women in group C became mildly depressed; these increases were statistically significant in group A (P=0.006) and group B (P=0.03).

Figure. 3.

Comparison among the studied groups regarding Patient Health Questionnaire-9 (PHQ-9) depression categories before and after 6 months. P-value for group A (combined injectable contraceptives users) is 0.006; for group B (combined oral contraceptives users) is 0.03; and for group C (intrauterine device users) is 0.09.

DISCUSSION

The findings of this study showed that there were statistically significant mild increases in the PHQ-9 scores of CIC users and COC users after the 6-month follow-up period (Table 3). Although there was no statistically significant difference between the groups in PHQ-9 score at the beginning of the study, after the 6-month follow-up period, a statistically significant difference (P<0.05) was observed, where group A, monthly combined injectable contraceptive users, had the highest mean value (5.2±2.1), followed by group B, the COC users, (4.6±2.03) (Table 2).

Previous studies have revealed that emotion regulation areas such as the amygdala and the hypothalamus contain estrogenic receptors, and animal studies have shown that both estrogen and progesterone modulate the synthesis of neurotransmitters, such as serotonin [13]. The types of synthetic progestins vary and can cross the blood-brain barrier [14]. Other researchers have found that oral contraceptive users have blunted responses to stress tests [15].

Consistent with our study, Anderl et al. [16] reported that there is a long-term association between adolescent oral contraceptive use and depression risk in adulthood, regardless of current oral contraceptive use, suggesting that adolescence may be a sensitive period during which oral contraceptive use could increase women’s risk of depression, even years after the first exposure. In addition, de Wit et al. [17] in 2020 concluded, in a prospective cohort study conducted to investigate the association between oral contraceptive use and depressive symptoms, that although oral contraceptive use showed no association with depressive symptoms, the monitoring of depressive symptoms in adolescents who use oral contraceptives is important, as the use of oral contraceptives may affect their quality of life and put them at risk of non-adherence.

According to Lundin et al. [6] in 2016, COC use is associated with small but statistically significant mood side effects during the intermenstrual phase. These findings are driven by a subgroup of women who clearly suffer from COC-related side effects. However, positive mood effects were noted in the premenstrual phase, and the proportion of women with clinically relevant mood worsening did not differ between the different treatment groups. Conversely, a double-blinded randomized placebo-controlled trial conducted by Zethraeus et al. [18] in 2017 found that COC had no effect on depressive mood.

After the 6-month follow-up period in our study, approximately 34.1% and 27.5% of the study groups moved from the non-depression stage to mild depression in CIC and COC users, respectively.

Hall et al. [19] in 2015 in his review article suggested that modern contraceptives with a lower dosage of steroids do not have a clinically relevant impact on women’s mood, as compared to higher doses of steroids that were used during the 1970s when depression was a known side effect of oral contraceptives use.

In agreement with our study, a prospective cohort study conducted by Skovlund et al. [20] in 2016 on women and adolescents aged 15 to 34 years in Denmark with no history of prior depression diagnosis, found that those who used hormonal contraceptives had a greater risk of developing depression within 6 months of using contraceptives than those who did not use contraceptives. They thus concluded that the use of hormonal contraception, especially rings, patches, or progesterone-only forms, was associated with the subsequent use of antidepressants, and the first diagnosis of depression, suggesting depression as a potential adverse effect of hormonal contraceptive use, particularly among adolescents.

Although some of these contraceptive methods are combined, differences in side effects according to the methods of delivery have been; for example, the risk of depression is higher with long-acting reversible contraceptive methods than with oral contraceptive pills. Consequently, different kinds of hormonal contraceptives containing different doses, types, and ratios of estrogen and progestin may affect the mode and central nervous system differently. Our study suggests that only some women are susceptible to these side effects, but we could not determine which group is more prone to depression; thus, medical care providers need to be aware of this possible risk, and provide counseling in addition to following up our patients effectively.

Although not significantly different, in our study the risk of depression was higher in combined injectable users that in those who used oral contraceptives. This knowledge would help medical care workers to choose the most suitable contraceptive methods for susceptible patients, while providing patients with more comprehensive information regarding the safety concerns of using these methods, especially for patients who were previously diagnosed or had received treatment for major depression.

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