Background
Major depression is the leading cause of the global burden of disease today [
1]. It is also the most prevalent psychiatric disorder during pregnancy [
2]. Prenatal depression can lead to serious health risks for both the mother and infant [
3,
4]. A recent systematic review revealed that in low- and lower-middle-income countries (LMICs) average prevalence of perinatal mental disorder (25.3%: 95% CI: 21.4–29.6%) was considerably higher than the 7–15% prevalence in high-income countries [
2]. Nonetheless, low-income countries assign about 0.5% of their health budget to mental health while high-income countries devote 5.1%, an amount, still disproportionately small (given the prevalence and impact of mental disorders), to implement a series of highly cost-effective interventions [
1].
In Ethiopia the prevalence of prenatal depression varies widely based on the instruments used and study settings. A 12% prevalence of prenatal depression was reported using PHQ-9 scale [
4], 23% using Beck Depression Inventory (BDI) scale [
5], 25% using Edinburgh Postnatal Depression Scale [
6] and 31.5% using WHO Self-Reported Questionnaire with 20 items (SRQ-20) [
7]. A community based study showed a 12% prevalence of common mental disorder during pregnancy [
4]. Whereas, health facility based studies revealed 23–31.5% prevalence [
5‐
7].
Based on previous research findings in low, middle and high income countries, socio-demographic factors such as age [
5,
8], income [
9] and educational attainment [
7] were identified as factors affecting prenatal depressive symptoms. Clinical factors includes previous depression [
8], concomitant high anxiety in pregnancy (Strewart et al., 2003) and a history of miscarriage and induced abortion [
10,
11]. Studies also showed that household food insecurity [
12] and anaemia [
13] are identified as nutrition related factors for prenatal depression. A number of studies also indicated that intimate partner violence is another factor associated with depression during pregnancy [
14,
15].
Several studies have shown a role of nutrition in mental distress, and they mostly documented the psychological effects of nutrient deficiencies. These studies indicated that deficiencies in folate, vitamin B12, calcium, iron, selenium, zinc, and polyunsaturated fatty acids (PUFAs) are associated with depression. Particularly, omega-3 fatty acids are getting special attention regarding their efficacy in depression treatment [
16]. Nutrition is a modifiable risk factor, and therefore is possible to be improved with targeted programs in addition to support programs to reduce maternal distress [
17].
Studies exploring the association between maternal nutrition and prenatal depression are still inconclusive and the limited studies available did not control for important variables such as intimate partner violence and social support [
18]. In Ethiopia, though the prevalence and determinants of intimate partner violence is well studied in the general population, there are limited data describing its association with prenatal depression [
19]. This study aims to describe the prevalence of prenatal depression and whether it is associated with maternal nutrition, intimate partner violence and social support among pregnant women in rural Ethiopia.
Methods
This study utilizes baseline data from a prospective, community-based, quasi-experimental birth cohort study within Empowering New Generations to Improve Nutrition and Economic opportunities (ENGINE) program. ENGINE is a USAID funded program, which aims to improve nutritional status of mothers’ and young children in Ethiopia through a multi-sectoral approach targeting health, nutrition and agriculture. The ENGINE birth cohort study was led by Tufts University and aimed to investigate the benefits of an integrated nutrition program and its co-location with agricultural growth program on household agricultural production and productivity, food security, diet diversity, socio-economic status and livelihoods, as well as health status, anthropometry and hemoglobin for mother and her child.
This study had an open cohort design, with rolling recruitment and follow up of pregnant women for a period of two years. The study was conducted from March 2014 to March 2016 in three Districts (Woliso, Tiro-Afeta and Gomma) in the South Western part of Ethiopia. A total of 4680 pregnant women were recruited between 12 to 32 weeks of gestation and followed up until 12 months postpartum. Data was collected once during pregnancy for all women (twice for those in the first trimester at recruitment), at birth, and then every three months until the child was 12 months old. Data collection was conducted by trained nurses electronically using Open Data Kit (ODK) software on handheld tablets and submitted to a secured server via an internet connection. Ethical clearance was obtained from Jimma University ethical review board. Informed written consent was obtained from all individual participants included in the study. All interviews were conducted in private and confidentiality was ensured for each study participants.
Data analysis
The data was analyzed using SPSS version 20. Bivariate and multivariate logistic regression analyses were computed to examine the relationship between the independent variables and prenatal depressive symptoms. The binary form of the dependent variable was coded as “1” for prenatal depressive symptoms (PHQ-9 score > = 8) and “0” for the absence (PHQ-9 score < 8). First binary logistic regression analyses were conducted between each individual independent variable and prenatal depressive symptoms. The findings were reported using unadjusted Odds Ratios (OR) and its 95% confidence interval (CI).
Then a full model including the nutritional (household food insecurity, anaemia, MUAC, fasting, nutrition related knowledge) socio-demographic (age, religion, marital status, family size and wealth index) and other confounders (obstetric factors, acute illnesses, social support, chat chewing practices and intimate partner violence) were fitted using a multivariate binary logistics regression to identify the independent predictors of prenatal depressive symptoms. Adjusted odds ratios (OR) and their 95% CI were presented as indicators of strength of association. A p-value of 0.05 or less was used to determine the cut-off points for statistical significance.
Discussion
The key contribution of this paper is to show the prevalence of prenatal depressive symptoms and its association with nutrition related factors, intimate partner violence and social support in rural Ethiopia. This finding has important implications, particularly in Ethiopia, where the burden of mental health diseases and intimate partner violence are high, resource allocation towards mental health care is poor with four psychiatrists per 10,000,000 population [
27], inadequate nutritional status in pregnancy is still a considerable public health burden and both nutrition and intimate partner violence are modifiable risk factors.
The relationship between IPV, depression and food insecurity are all bidirectional and social support plays a buffering and protective role in this link. Depression is the most common mental health consequences of IPV [
28,
29]. Previous studies indicated that women who experience IPV have about four times greater risk of depression than women who do not experience IPV. On the other hand, depression is associated with the use of hostility, insult, and threat in marital interactions [
30,
31]. When we see the pathway between IPV and household food insecurity, previous research demonstrated that it is mediated by depression [
32].
Poverty is one of the key contributors to intimate partner violence [
33]. Since poverty is inherently stressful, it has been argued that intimate partner violence may result from stress and that poorer men have fewer resources to reduce stress. Poverty as it impairs purchasing power, results in household food insecurity. IPV may affect the couple’s capacity to organize the home environment and manage the resources available in order to guarantee the food and nutrition security of the family. Looking this link from household food insecurity side, a broader anthropological conceptualization of food insecurity posits that acute or chronic exposure to periods of food uncertainty can influence mental and physical health outcomes. Social support plays a buffering role for both depressive symptoms and IPV. Social support from family or friends buffers the effects of environmental stressors such as IPV and poverty and could decrease individual’s vulnerability to depression [
34].
Consistent with previous studies in low, middle and high income countries, this study revealed that household food insecurity is strong predictor of prenatal depressive symptoms [
12,
35‐
38]. Food insecurity by itself is a stressful life event, and the occurrence of stressful events was shown to affect the hypothalamic-pituitary-adrenocortical (HPA) axis. It is also known that hypothalamic dysfunction was linked to the onset and recurrence of depression [
39].
Moreover, previous studies indicated that food insecurity was linked to specific nutrient deficiencies, which were also associated with depressive symptoms [
16,
40]. These studies showed that food insecurity influences prenatal depression through deficiencies in energy, vitamin B12, Selenium or folic acid. Yet, another study also indicated that low-income women with depressive symptoms and life stressors represent an at-risk group for low diet quality during pregnancy and hence the link between depression and nutrient deficiencies is bidirectional [
41]. Using nationally representative data and a number of different modeling approaches, Noonan and colleagues found robust evidence that maternal depression has adverse effects on household food insecurity [
42]. Hence, the association between depression and food insecurity is also bidirectional.
In this study, pregnant women with depressive symptoms had lower haemoglobin levels than women without depressive symptoms. In agreement with our findings, previous observational studies generally established that anaemia is associated with depression [
13,
43]. However, a placebo and high-iron diet controlled supplementation trial among female participants in high income countries found no association between depression and anaemia [
44].
The relationship and direction of the relationship between depression and maternal anaemia remains unclear and still needs further investigation. However, there are different hypotheses about the mechanisms linking anaemia with depression. Iron is a co-factor in synthesis of tyrosine and tryptophan. Tyrosine and tryptophan are precursors for the neurotransmitters dopamine, norepinephrine and serotonin [
45]. The traditional monoamine hypothesis of depression speculates that low dopamine, norepinephrine, and serotonin concentrations may result in depression [
46]. In addition, iron is a cofactor for the reaction leading to the production and secretion of glutamate [
47]. The glutamate hypothesis of depression has posited that dysregulation of the glutamatergic system results in depression [
48].
In congruence with other previous studies, we found a statistically significant association between intimate partner violence and prenatal depressive symptoms [
14,
15,
49]. Because of fear of stigmatization, battered women often experience feelings of shame, isolation and entrapment and did not communicate openly to others that violence occurred to them by their spouses [
50]. This results in lack of support from friends and families and rather leads to more depression.
Respondents with prenatal depressive symptoms reported poorer maternal social support compared to their counterparts. Our finding is consistent with the suggestion that social support may safeguard the adverse effects of prenatal psychological distress on birth outcomes [
51,
52]. The buffering hypothesis of social support postulated that the potential pathogenic effect of stressful events is reduced when support is accessible [
53].
The prevalence of depressive symptoms during pregnancy in our study was lower compared to previous prevalence reports in Ethiopia [
4‐
7,
54]. The relatively lower prevalence in our study probably reflects the fact that this is a population based study while the prior studies were health facility based. It could be postulated that the difference in rates could be due to different population sub-groups, for example in the health facility based studies, respondents are likely to be medical patients who may be reporting somatic symptoms (e.g. fatigue and anorexia) that might be confounded by the underlying condition that the patients are seeking care. Spitzer et al. [
55] recommended that tools with questions about appetite, fatigue, or sleep (e.g., PHQ-9) must be interpreted cautiously, as impairment might reflect the physical effect of pregnancy rather than depressive symptoms.
We found a statistically significant difference in prenatal depressive symptoms prevalence among the three study districts with the lowest prevalence found in Woliso. Worldwide estimates of depressive symptoms vary widely between studies and settings, discrepancies being attributable to real differences between countries but also to the method of assessment [
56]. Previous studies in Ethiopia reported a differential prenatal depressive symptoms prevalence by study sites [
4‐
7]. Each of these studies used different tools to screen depressive symptoms.
Adjusting for relevant confounding variables, we found that marital status, geographical location, family size, household food insecurity and anaemia were identified as predictors of prenatal depressive symptoms. The association between marital status and prenatal depressed mood is consistent with a number of studies in low, middle and high income countries where they found higher rates of mental distress in the widowed, separated and divorced women in comparison with married women [
57,
58]. However, other general population studies reported no association [
59,
60].
The main strength of this study lies in access to community based data to describe prevalence and associated risk factors of depressive symptoms during pregnancy. This study is also based on large sample size and huge response rate; a very thorough description of the population with a big number of questionnaires on different socio-demographic, nutritional and other clinical risk factors. Being a cross-sectional analysis, the usual restrictions inherent to cross-sectional and observational studies apply here; no information about causality. An additional limitation of this study is that we used one month recall on the food-insecurity measure, but a two weeks recall on the measure of depressive symptoms, which raises concerns over the reported associations.
Conclusions
Prenatal depressive symptomatology is quite common during pregnancy. Socio-demographic factors such as marital status, family size and geographical location are associated with an increased prevalence of prenatal depressive symptoms. Similarly, nutrition related factors such as household food insecurity and anaemia are associated with prenatal depression. While social support from friends, families and spouse during pregnancy are protective, intimate partner violence augments prenatal depression.
The implications of our study for practice are to emphasize the need for targeted screening for intimate partner violence and depressive symptoms during pregnancy and to link cases to health facilities where treatment is available. In this regard we recommend the Ethiopian Ministry of Health to integrate screening of depressive symptoms and intimate partner violence in routine antenatal care services. Policies aimed at reducing household food insecurity, maternal anaemia, intimate partner violence and promoting maternal social support are likely to have a significant public health impact in preventing prenatal depression. Organizing a mental health team, including health extension workers, in antenatal services to screen and treat prenatal depression together with the aforementioned risk factors during pregnancy might prevent or ameliorate prenatal depression.