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Indian Journal of Psychiatry logoLink to Indian Journal of Psychiatry
. 2022 Jun 8;64(3):284–288. doi: 10.4103/indianjpsychiatry.indianjpsychiatry_1318_20

Impact of perinatal maternal depression on child development

Rita Roy 1,, Madhushree Chakraborty 1, Kaberi Bhattacharya 2, Turna Roychoudhury 1, Suchandra Mukherjee 1
PMCID: PMC9290416  PMID: 35859561

Abstract

Background:

As India reduced maternal mortality by 50% in the last decade, the mental health of mothers has slowly started catching our attention. Increased participation of women in the economic sector and awareness of women’s rights has added to this process. Perinatal depression has been associated with negative birth outcomes and poor child development. The paucity of research from eastern India poses challenges for physicians and hinders effective medical interventions.

Aim:

To investigate the effect of antenatal and postnatal depression on child development at 12 months of age.

Method:

In total, 174 mothers were administered Bengali Edinburgh Postnatal Depression Scale (EPDS-B) for assessment of antenatal and postnatal depression. Developmental Assessment Scale in Indian Infants (DASII) was administered to assess the motor and cognitive development of their children (n = 153) at 12 months.

Result:

The prevalence of antenatal and postnatal depression was 28.7% and 16.7%, respectively. Antenatal depression predicted postnatal depression (b = 0.631). Mothers with AD scored significantly low on family support measures (P = 0.012). Children of mothers with AD had low motor and cognitive attainment at the age of 12 months (P = 0.022).

Conclusion:

Screening and treatment of mental health need to be included in the antenatal care routine to facilitate appropriate child development.

Keywords: Antenatal, child development, maternal depression, postnatal

INTRODUCTION

Pregnancy brings about a huge transition in women’s life. Traditionally, it is presumed to be uniquely fulfilling and emotionally satisfying—so much so that women may feel pressured to be happy.[1] However, harsh social and material realities can force women into mental distress during pregnancy.[1,2] Coping with the physical[3] and physiological[4] changes that take place to accommodate the growing fetus can also bring about unprecedented emotional distress.[3,4,5] Consequently, non-psychotic mental disorders such as stress, anxiety, and depression are quite common in the antenatal as well as postnatal stages.[6,7] According to a recent review, psychiatric illness in Indian women has escalated in general and in the perinatal period in particular.[8]

Both antenatal[9] and postnatal[10] emotional distress can result in negative birth outcomes and poor developmental attainment.[9,10,11] However, while postnatal mental health issues have received significant attention, antenatal mental health problems remain far less explored[12] despite it being no less common than postnatal mental health illnesses.[13,14] The medical myth regarding hormonal protection against psychological distress during pregnancy,[15] coupled with social expectations from expecting mothers may cumulate to disregard and suppress the personal experience of emotional distress. Consequently, the effect of antenatal emotional distress on birth outcomes and development of children remains relatively unexplored.

So far, no study from eastern India has been conducted to investigate how non-psychotic mental disorders in pregnant women might influence the growth and development of their children. A systematic review of Indian studies on antenatal depression (AD) draws attention toward the dearth of studies from the eastern part (n = 0).[14] The paucity of research from eastern India (n = 3) has also been noted in a systematic review and meta-analysis of postpartum depression (PND) in India.[16]

Perinatal depression, defined as depression occurring in a woman anytime during her pregnancy and within 12 months of delivery, has a wide variability in prevalence, predictors, and impacts in different populations.[17] Consequently, population-specific data can help plan effective intervention measures. In this study, we investigated the effect of AD and PND on children’s developmental parameters. We also explored the association between AD and PND.

METHODS

Participants: Literate mothers between 12 and 36 weeks of pregnancy attending the antenatal clinic at the Institute of Post Graduate Medical Education and Research and SSKM Hospital, Kolkata between March 1 and April 30, 2019 were invited to participate in this study. Mothers with twin pregnancies or with chronic medical or psychotic illnesses were excluded from the study. Participants signed an informed consent form approved by the institutional ethics committee. In total, 174 mothers and their babies (male: 93, female: 81) participated in this study [Table1]. Only 153 mothers turned up with their babies for the third session, which was conducted 1 year after delivery.

Table 1.

Demographic details of participants

n> Range> Minimum> Maximum> Mean> SD>
Age 174 24 18 42 25.73 4.279
Education 174 17 0 17 10.39 4.315
Socioeconomic status 174 5 1 6 3.74 0.711
Family support 174 32 0 32 5.90 3.627

Materials: A semi-structured questionnaire was used to record the age, literacy, occupation, and family income of the participants. Modified Kuppuswamy socioeconomic scale[18] was used to evaluate socioeconomic status. Family support scale (FSS)[19] was used to find out the extent of support these mothers received from spouse, family members, relatives, friends, neighbors, and community in the perinatal period.

Bengali version of the Edinburgh Postnatal Depression Scale (EPDS-B)[20,21] was administered to assess AD and PND. It is an adaptation of the original English version of EPDS. The EPDS is a self-rated questionnaire where participants are asked to respond to 10 questions that assess objectively how they felt in the last 7 days. The responses are coded from 0 to 3, with 0 meaning no distress and 3 meaning severe distress. A summed-up figure is the final score. The minimum score is 0 and the maximum 30. In this study, a score of 13 was considered as the threshold.[21]

EPDS has proved to be an effective tool for assessing PND in the Indian population.[22] Although EPDS was designed to assess PND, several studies have used it to measure AD as well.[23,24] Hence, we used EPDS-B to assess both AD and PND.

Developmental Assessment Scale in Indian Infants (DASII)[25] was administered to the children at 12 months to test their motor and cognitive development. DASII was adapted from the Bayley Scale of Infant Development (BSID).[26] The DASII is an effective and comprehensive tool that has been standardized on Indian babies by Dr. Phatak. It is applicable for infants between 0 and 30 months. It involves guided play activity using play material designed for the purpose. Independent motor and mental developmental quotients are generated based on the performance of the babies during the test.

Procedure: The study was conducted in three sessions. In the first session, participants (pregnant mothers between 12 and 36 weeks of pregnancy) completed the demographic datasheet and EPDS-B in a quiet room of the hospital. The second session was conducted 3–6 months after delivery. The EPDS and FSS were administered to all the participating mothers in this session. The third session was conducted 1 year after the delivery. Developmental Assessment Scale in Indian Infants (DASII) was administered to the infants of the participating mothers in this session. A psychologist trained and certified in DASII collected the data in the designated room of the early intervention clinic.

Statistical analysis

Data were analyzed using SPSS Statistics 21.0 (IBM Corp., Armonk, NY, US). Descriptive statistics and t tests were used to characterize the demographic parameters. One-way MANCOVA was conducted with motor and cognitive scores of the babies as the dependent variables, group (mothers with and without AD) as the independent variable, and PND as the covariate. Another one-way MANCOVA was conducted with motor and cognitive scores of the babies as the dependent variables, group (mothers with and without PND) as the independent variable, and AD as the covariate. Linear regression was also carried out to investigate if there exists a linear relationship between AD and PND.

RESULT

It was found that 28.7% (50/174) of the mothers had AD and 16.7% (29/174) had PND. In total, 31.6% (55/174) had perinatal depression [Figure 1].

Figure 1.

Figure 1

Prevalence of AD, PD, and perinatal depression

AD (b = 0.631, t = 10.663, P < 0.001) predicted PND in pregnant women (F (1, 172) = 113.7, P < 0.001, R2 = 0.398, Cohen’s f2 = 0.661).

There was no significant difference between mothers with and without AD in age (P = 0.830), education (P = 0.655), and socioeconomic status (P = 0.987). However, mothers with AD scored significantly low on family support measures (P = 0.012) [Table 2]. Mothers with and without PND were comparable in age (P = 0.339), education (P = 0.294), socioeconomic status (P = 0.476), and family support measures (P = 0.145).

Table 2.

Details of women with and without perinatal depression and their babies

Perinatal depression n Mean Sth. Deviation t P
Age No perinatal depression 119 25.78 3.981 0.233 0.816
Perinatal depression 55 25.62 4.901
Education No perinatal depression 119 10.71 4.251 1.459 0.146
Perinatal depression 55 9.69 4.409
Socioeconomic status No perinatal depression 119 3.73 0.756 −0.280 0.780
Perinatal depression 55 3.76 0.607
Family support No perinatal depression 119 6.36 3.864 2.525 0.012
Perinatal depression 55 4.89 2.833
Gestation age in weeks No perinatal depression 119 36.07 3.124 −1.123 0.263
Perinatal depression 55 38.67 3.672
Birth weight in g No perinatal depression 119 2431.71 775.164 0.686 0.494
Perinatal depression 55 2342.38 848.944

There was a statistically significant difference between the children of mothers with and without AD on the combined developmental parameters after controlling for PND, F (2, 149) = 3.899, P = 0.022, Wilks’ L = 0.950, and partial h2 = 0.050. Pairwise comparisons with Bonferroni correction indicated that the mean cognitive development scores of children of mothers without AD (M = 93.9, SD = 11.3) was significantly higher than the children of mothers with AD (M = 86.9, SD = 11.6) (P = 0.006, Cohen’s d = 0.61) [Figure 2]. The mean motor development scoresof children of mothers without AD (M = 95.7, SD = 12.4) were higher than those of the children of mothers with AD (M = 90.4, SD = 12.5). This difference was not statistically significant (P = 0.325), but the effect size was not insignificant (Cohen’s d = 0.427).

Figure 2.

Figure 2

Cognition and motor development with or without antenatal depression

There was no statistically significant difference between the children of mothers with and without PND on the combined developmental parameters after controlling for AD, F (2, 149) = 1.450, P = 0.238, Wilks’ L = 0.981, and partial h2 = 0.019.

DISCUSSION

We investigated the impact of maternal depression on the motor and cognitive development of children. The prevalence of perinatal depression was found to be 31.6%. This rate is higher than that found in the studies from north India (14%)[27] and central India (12.4%).[17]

The prevalence of AD in this study was found to be 28.7%. The result is quite consistent with that reported by Maheshwari et al.[28] (AD = 24.8%) and Rehman et al.[29] (AD = 26%), who studied pregnant women attending antenatal clinics of urban/tertiary health care centers in Bangalore and Srinagar, respectively. Another study done in a tertiary care center of Karnataka reported a higher prevalence of AD (36.75%).[30] However, this study investigated a wider age range of pregnant women (15–45) than ours (18–42). A higher prevalence of AD (65%) was reported in a study from south India which investigated rural women near Chennai.[31] It may be noted that living in rural areas has been associated with an increased risk of perinatal mental illness.[32] The prevalence rate was low in Indian studies that used the Beck Depression Inventory Scale (BDI) to assess AD.[33,34] The prevalence rate found in our study (28.7%) is close to the one reported for Southeast Asian women (22.6%) in a recent meta-analysis study that used pooled samples, but it is higher than the country average (17.74%) reported in the same study.[35]

The prevalence of PND was found to be 16.7% in this study. This is lower than the pooled prevalence of PND in eastern India (23%) and the pooled prevalence of PND calculated for Indian women (22%).[16] However, two of the three studies from eastern India that were included in the meta-analysis had assessed PND within 2 weeks of delivery. Thus, the prevalence of PND in eastern India may be higher as the researchers had conflated baby blues with PND. AD predicted PND. This is consistent with the findings reported by Cury and Menezes, who investigated the association between AD and PND in the Brazilian population.[36] This is also consistent with the results by Kingston et al.,[37] who reviewed 2448 studies to investigate the association between antenatal and postnatal psychological distress.

Mothers with AD scored significantly low on family support measures. Though we measured AD during pregnancy and family support during the first 3–6 months postpartum, we anticipated that support from family and friends would remain the same in both antenatal and postnatal periods. This is consistent with several other studies that suggest the importance of family support in improving the mental health of pregnant women.[12,14,38] Lack of social and partner support was identified as the second most commonly associated risk factor for antenatal depression in four systematic reviews encompassing 47 primary studies consisting of around 226,000 participants.[39]

Children of mothers with AD had low motor and cognitive attainment at the age of 12 months. The difference in cognitive development was statistically significant. This is again quite in line with Kingston et al.[37] The authors stated that most studies obtained medium effect sizes for the association between antenatal psychological distress and cognitive development.

Our result is consistent with a growing body of literature that reports altered uterine physiology in response to maternal psychological state.[40] Maternal depression and anxiety can affect intrauterine artery blood flow. Increased uterine artery resistance restricts uterine blood flow, cutting down the supply of oxygen and nutrients to the growing fetus. This may affect the growth and development of the fetus. Also, maternal stress during pregnancy may increase the levels of cortisol and corticotrophin-releasing hormone in the mother and subsequently in fetal circulation. These hormones may contribute to behavior disorders and cognitive deficits, including attention and learning disorders.

There was no significant effect of PND on the developmental attainments of children when the effect of AD was controlled. It may be noted that the effect of PDD on developmental parameters has been reported to be inconclusive. Variable effect sizes were reported for the association between postnatal mental distress and cognitive development by Kingston et al.[37] However, further research is needed to confirm the long-term effects of PND on motor and cognitive development. A strong correlation between AD and PND suggests that the effect of PND on child development observed by some researchers may be primarily due to AD.

Small sample size, using a screening tool instead of a diagnostic test, and having the same cut-off scores for antenatal and PND were some of the limitations of the present study. Moreover, we did not consider all the factors such as planned versus unplanned pregnancy, multigravidity, history of abortion, phase of pregnancy, employment status, gender preference, domestic violence, and medication, which could affect maternal depression. We did not assess other non-psychotic mental health parameters such as anxiety and stress, which are reported to affect developmental attainments. Despite these limitations, this study provides much-needed preliminary information on perinatal mental illness among women in eastern India and its impact on child development. Future investigations on larger samples including all the important risk factors will help lend further insight.

CONCLUSION

The high prevalence of AD, its adverse effect on developmental attainments of children, and its positive correlation with PND indicate a pressing need to include mental health screening in antenatal care routine. An adequate and timely intervention of AD can help ameliorate the burden of postpartum depression and adverse child developmental attainments associated with perinatal depression.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

REFERENCES

  • 1.Sneha R. Are Indian mothers happy?The wire. 2018. Available from: https://thewire.in/health/are-indian-mothers-happy .
  • 2.Prost A, Lakshminarayana R, Nair N, Tripathy P, Copas A, Mahapatra R, et al. Predictors of maternal psychological distress in rural India:A cross-sectional community-based study. J Affect Disord. 2012;138:277–86. doi: 10.1016/j.jad.2012.01.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Meltzer-Brody S. New insights into perinatal depression:Pathogenesis and treatment during pregnancy and postpartum Dialogues Clin Neurosci. 2011;13:89–100. doi: 10.31887/DCNS.2011.13.1/smbrody. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Moya J, Phillips L, Sanford J, Wooton M, Gregg A, Schuda L. A review of physiological and behavioral changes during pregnancy and lactation:Potential exposure factors and data gaps. J Expo Sci Environ Epidemiol. 2014;24:449–58. doi: 10.1038/jes.2013.92. [DOI] [PubMed] [Google Scholar]
  • 5.Altshuler LL, Hendrick V, Cohen LS. An update on mood and anxiety disorders during pregnancy and the postpartum period. Prim Care Companion J Clin Psychiatry. 2000;2:217–22. doi: 10.4088/pcc.v02n0604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Satyanarayana VA, Lukose A, Srinivasan K. Maternal mental health in pregnancy and child behavior. Indian J Psychiatry. 2011;53:351–61. doi: 10.4103/0019-5545.91911. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Howard LM, Molyneaux E, Dennis CL, Rochat T, Stein A, Milgrom J. Non-psychotic mental disorders in the perinatal period. Lancet. 2014;384:1775–88. doi: 10.1016/S0140-6736(14)61276-9. [DOI] [PubMed] [Google Scholar]
  • 8.Harsha1 G, Acharya M. Trajectory of perinatal mental health in India. Indian J Soc Psychiatry. 2019;35:47–54. [Google Scholar]
  • 9.O'Connor TG, Monk C, Fitelson EM. Practitioner review:Maternal mood in pregnancy and child development-Implications for child psychology and psychiatry. J Child Psychol Psychiatry. 2014;55:99–111. doi: 10.1111/jcpp.12153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.A-C Bernard-Bonnin, Canadian Paediatric Society, Mental Health and Developmental Disabilities Committee. Maternal depression and child development. Paediatr Child Health (Oxford) 2004;9:575–83. [Google Scholar]
  • 11.Dunkel Schetter C, Tanner L. Anxiety, depression and stress in pregnancy:Implications for mothers, children, research, and practice. Curr Opin Psychiatry. 2012 doi: 10.1097/YCO.0b013e3283503680. doi:10.1097/YCO.0b013e3283503680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Biaggi A, Conroy S, Pawlby S, Pariante CM. Identifying the women at risk of antenatal anxiety and depression:A systematic review. J Affect Disord. 2016 doi: 10.1016/j.jad.2015.11.014. doi:10.1016/j.jad. 2015.11.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Evans J, Heron J, Francomb H, Oke S, Golding J. Cohort study of depressed mood during pregnancy and after childbirth. BMJ. 2001;323:257–60. doi: 10.1136/bmj.323.7307.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Arora P, Aeri B. Burden of antenatal depression and its risk factors in Indian settings:A systematic review. Indian J Med Spec. 2019;10:55–60. [Google Scholar]
  • 15. [[Last accessed on 2022 Apr 08]]. Available from: https://med.stanford.edu/womensneuroscience/wellness_clinic/Pregnancy.html .
  • 16.Upadhyay RP, Chowdhury R, Salehi A, Sarkar K, Singh SK, Sinha B, et al. Postpartum depression in india:A systematic review and meta-analysis. Bull World Health Organ. 2017;95:706–17C. doi: 10.2471/BLT.17.192237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Rathod SD, Honikman S, Hanlon C, Shidhaye R. Characteristics of perinatal depression in rural central, India:A cross-sectional study. Int J Ment Health Syst. 2018;12:68. doi: 10.1186/s13033-018-0248-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Saleem SM. Modified Kuppuswamy Scale Updated for Year 2018. Paripex- Indian J Res. 2018;7:6–7. [Google Scholar]
  • 19.Persha A, Sheilaja Rao VRP. Early Intervention to IUGR Children at Risk for Developmental Delays. secunderabad, AP: NIMH, Manovikasnagar; 2003. [Google Scholar]
  • 20.Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression:Development of the 10-item Edinburgh postnatal depression scale. Br J Psychiatry. 1987;150:782–6. doi: 10.1192/bjp.150.6.782. [DOI] [PubMed] [Google Scholar]
  • 21.Maity C, Saha S, Sanyal D, Biswas A. The Bengali adaptation of Edinburgh postnatal depression scale. IOSR-JNHS. 2015;4:12–6. [Google Scholar]
  • 22.Russell PSS, Chikkala SM, Earnest R, Viswanathan SA, Russell S, Mammen PM. Diagnostic accuracy and clinical utility of non-English versions of Edinburgh Post-Natal Depression Scale for screening post-natal depression in India:A meta-analysis. World J Psychiatry. 2020;10:71–80. doi: 10.5498/wjp.v10.i4.71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Faleschini S, Rifas-Shiman SL, Tiemeier H, Oken E, Hivert MF. Associations of prenatal and postnatal maternal depressive symptoms with offspring cognition and behavior in mid-childhood:A prospective cohort study. Int J Environ Res Public Health. 2019;16:1007. doi: 10.3390/ijerph16061007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Bavle AD, Chandahalli AS, Phatak AS, Rangaiah N, Kuthandahalli SM, Nagendra PN. Antenatal depression in a tertiary care hospital. Indian J Psychol Med. 2016 doi: 10.4103/0253-7176.175101. doi:10.4103/0253-7176.175101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Patni B. Developmental assessment scales for Indian infants (DASII) Indian J Pract Pediatr. 2012;14:409–12. [Google Scholar]
  • 26.Nancy B. Bayley scales of infant and toddler development:administration manual. San Antonio, TX: Harcourt Assessment; 2006. [Google Scholar]
  • 27.Sidhu G, Sidhu T, Kaur P, Lal D, Sangha N. Evaluation of peripartum depression in females. Int J Appl Basic Med Res. 2019;9:201–5. doi: 10.4103/ijabmr.IJABMR_23_19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Maheshwari M, Divakar SV. A cross sectional study on mental health status of pregnant women at urban health centre of Bangalore, India. Int J Community Med Public Heal. 2016 doi:10.18203/2394-6040.ijcmph 20160925. [Google Scholar]
  • 29.Rehman BU, Ahmad J, Kaul RUR, Haque MK ul. An epidemiological study to assess the mental health status of pregnant women in a tertiary care hospital, Srinagar, Jammu and Kashmir, India. Int J Reprod Contraception, Obstet Gynecol. 2017 doi:10.18203/2320-1770.ijrcog20172355. [Google Scholar]
  • 30.Hegde S.S., Pai KK, Abhishekh HA, Sandeep KR. Prevalence of antenatal depression and gender preference:A cross sectional study among Mangalore population, Karnataka, India. J Pharm Biomed Sci. 2013;30:1011–4. [Google Scholar]
  • 31.Srinivasan N, Murthy S, Singh AK, Upadhyay V, Mohan SK, Joshi A. Assessment of burden of depression during pregnancy among pregnant women residing in rural setting of Chennai. J Clin Diagnostic Res. 2015;9:LC08–12. doi: 10.7860/JCDR/2015/12380.5850. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Ginja S, Jackson K, Newham JJ, Henderson EJ, Smart D, Lingam R. Rural-urban differences in the mental health of perinatal women:A UK-based cross-sectional study. BMC Pregnancy Childbirth. 2020;20:464. doi: 10.1186/s12884-020-03132-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Ajinkya S, Jadhav P, Srivastava N. Depression during pregnancy:Prevalence and obstetric risk factors among pregnant women attending a tertiary care hospital in Navi Mumbai. Ind Psychiatry J. 2013;22:37–40. doi: 10.4103/0972-6748.123615. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Shrestha N, Hazrah P, Sagar R. Incidence and prevalence of postpartum depression in a rural community of India. J Chitwan Med Coll. 2015;5:11–9. [Google Scholar]
  • 35.Mahendran R, Puthussery S, Amalan M. Prevalence of antenatal depression in South Asia:A systematic review and meta-analysis. J Epidemiol Community Health. 2019 doi: 10.1136/jech-2018-211819. doi:10.1136/jech-2018-211819. [DOI] [PubMed] [Google Scholar]
  • 36.Faisal-Cury A, Menezes PR. Antenatal depression strongly predicts postnatal depression in primary health care. Rev Bras Psiquiatr. 2012;34:446–50. doi: 10.1016/j.rbp.2012.01.003. [DOI] [PubMed] [Google Scholar]
  • 37.Kingston D, McDonald S, Austin MP, Tough S. Association between prenatal and postnatal psychological distress and toddler cognitive development:A systematic review. PLoS One. 2015 doi: 10.1371/journal.pone.0126929. doi:10.1371/journal.pone. 0126929. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Hu Y, Wang Y, Wen S, Guo X, Xu L, Chen B, et al. Association between social and family support and antenatal depression:A hospital-based study in Chengdu, China. BMC Pregnancy Childbirth. 2019;19:420. doi: 10.1186/s12884-019-2510-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Dadi AF, Miller ER, Bisetegn TA, Mwanri L. Global burden of antenatal depression and its association with adverse birth outcomes:An umbrella review. BMC Public Health. 2020;173:20. doi: 10.1186/s12889-020-8293-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Field T. Prenatal depression effects on early development:A review. Infant Behav Dev. 2011;34:1–14. doi: 10.1016/j.infbeh.2010.09.008. [DOI] [PubMed] [Google Scholar]

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