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. 2015 Jul 30;8(4):120–126. doi: 10.5539/gjhs.v8n4p120

The Association Between Postpartum Depression and Pica During Pregnancy

Neda Ezzeddin 1, Roza Zavoshy 1, Mostafa Noroozi 2,, Mohammad Ebrahim Sarichloo 3, Hassan Jahanihashemi 2
PMCID: PMC4873575  PMID: 26573027

Abstract

Introduction and Objectives:

Postpartum depression (PPD) is a common disorder and social debilitating that has adverse effects on the mother, child and family. Pica is an eating disorder characterized by persistent ingestion of substances that the consumer does not define as food. The aim of this study was to investigate the association of postpartum depression with pica during pregnancy.

Method:

This is case-control study was carried out in health centers in west Tehran. 152 depressed women (case group) and 148 non-depressed women (control group) were selected randomly from these health care centers. In addition to collecting demographic and pica data, the Edinburgh Depression Scale was used. The data was analyzed by both descriptive and analytic analyses such as chi-squared and logistic regression in SPSS version 16.

Result:

In this study, there wasn’t a significant association between PPD and pica during pregnancy (P=0.153, OR=2.043, CI=0.767, 5.438), but, postpartum depression has a significant association with type (clay) (P= 0.024) and duration (more than 2 months) (P= 0.023) of pica practice.

Conclusions:

In the present study, pregnancy pica was not important risk factor for PPD but there were similar risk factors such as iron supplementation during and postpartum pregnancy with pica and PPD.

Keywords: Postpartum depression, pica, pregnancy

1. Introduction

Postpartum depression (PPD) is a common and socially debilitating disorder, with adverse effects on mother, infant and family (Field, 2010). PPD is characterized by a depressed mood, excessive anxiety, insomnia and change in weight. The onset is generally within 12 weeks after delivery (Sadock & Sadock, 2008). Its etiology remains unknown, but risk factors affecting PPD includes: genetic predisposition, environmental, social, psychological and biological factors (Leung & Kaplan, 2009).

Eating disorders such as anorexia nervosa and bulimia have potentially adverse consequences on pregnancy including increased miscarriage, low birth weight, labor complications, and PPD. Symptoms of pregnancy and PPD are more prevalent among women with a history of eating disorders, and both anorexia nervosa and bulimia are associated with PPD (Leddy, Jones, Morgan, & Schulkin, 2009; Mazzeo et al., 2006).

Pica is an eating disorder characterized by continuous ingestion of substances that the eater does not consider as food including: earth, soil or clay (Geophagia), corn or laundry starch (Amylophagia) and ice or freezer frost (Pagophagia) (Mensah, Twumasi, Amenawonyo, Larbie, & Jnr, 2010; Young et al., 2010).

Pica is usually seen among pregnant and lactating women, children, the mentally lagged, and those with mental problems. Pica is not limited to a geographical area, race, sex, culture, or social position (Mortazavi & Mohammadi, 2010), and its prevalence during pregnancy varies from 0.02% to 74% (Boatin et al., 2012). The prevalence of pica in pregnant women has been reported 15.5% in Zahedan (a city in the southeastern of Iran) (Mortazavi & Mohammadi, 2010) and 22.3% in Kermanshah (a city in the West of Iran) (Rezavand & Rawshani, 2006). Etiology of pica is unknown, but some hypotheses attribute pica to deficiency of nutrients such as iron, calcium, copper, zinc, etc., leading to consumption of inedible substances containing these nutrients (Janbabai et al., 2011).

Many people with pica are ashamed to express it, as they consider it a mental disorder. Yet, it poses harmful consequences such as intestinal obstruction and perforation, preterm labor, mercury and lead poisoning, hyper- and hypokalemia, obesity, nutritional deficiency in pregnancy, anemia, iron deficiency, etc (Grotegut et al., 2006; Thihalolipavan, Candalla, & Ehrlich, 2013).

Previous studies have demonstrated the relationship of eating disorders such as anorexia nervosa and bulimia with PPD. However, few studies have investigated the relationship between PPD and pica. Since etiologies of pica and PPD are unknown, this study aims to determine the relationship between PPD and pregnancy pica.

2. Methods

2.1 Study Population, Design and Data Collection

This case-control cross-sectional study was carried out from March to May 2014, among women who had referred to health care centers supported by Shahid-Beheshti University of Medical Science in the west of Tehran. Eight urban health care centers were selected by random sampling among 16 centers. These 8 centers provided a good distribution of all 16 centers based on covered population and geographic area.

152 depressed women (case group) and 148 non-depressed women (control group) were selected randomly from these health care centers. Sampling technique was stratified (each center as stratum), number of samples for each center was proportional to the size of it.

The inclusion criteria were considered being 18-45 years old; 3-8 months elapsed from their delivery, with no history of depression and chronic disease (such as cardiovascular disease, diabetes, cancers and endocrine disease) and consent to participate in the study.

A two-part questionnaire was used, containing demographic details such as age, education, occupation, infant's gender, pregnancy ranks, history of abortion or stillbirth, and also pregnancy pica.

The questionnaire of pica during pregnancy included: the kind (ice, freezer frost, soil, rosary and praying clay, raw starch, cigarette ashes, oil or petrol, baking soda, tobacco, charcoal and or any other non-food substances that eaten during pregnancy and not listed above), the onset, duration, frequency (daily, weekly or monthly) and the reasons (unable to give them, satisfy craving, relief of nausea, reduced stress and anxiety and or other reasons) of pica practice.

2.2 Measures

2.2.1 Assessment of Depression

To identify women with PPD, Edinburgh Postpartum Depression Scale (EPDS) was used, which contains 10 items on the person's feelings over the past 7 days, each with 4 options, scoring from 0 to 3, with maximum score of 30 and minimum of zero. In this study, women scoring above 10 were considered depressed, and those scoring 10 and below, non-depressed. This is a standard and approved questionnaire with reliability of 0.9 and in Persian language (Alipour, Lamyian, & Hajizadeh, 2012).

2.2.2 Anthropometric Assessment

Mothers’ height was measured in standing position, with no shoes, heels touching the wall, and face looking forward using Seca stadiometer with the precision of 0.1 cm. Mothers’ weight was measured wearing minimum clothing and no shoes using Seca digital weighing scales. BMI was calculated by dividing weight (kg) over height squared (m2).

2.3 Statistical Analysis

The data were analyzed using statistical tests, including chi-squared, logistic regression, using the Statistical Package for Social Sciences version 16 (SPSS Inc., Chicago, IL, USA).

3. Results

Mean age was 28.61±6.07 years in depressed group and 28.82±5.22 years in non-depressed group. Case (152 women) and control (148 women) groups were matched in terms of age, BMI, infant's sex, pregnancy ranks, and history of abortion or stillbirth. The result of study showed no association between mother's occupation and PPD (P=0.441). The prevalence of under diploma women in depressed group was significantly higher than non-depressed group (P=0.033) (Table 1).

Table 1.

The association between PPD and some demographics and obstetrics variables among studied mother

Variables depressed Non-depressed P-value*
(%)N (%)N
Mother age
<26 48(52.2) 44(47.8)
26-34 81(50) 81(50) 0.941
35> 23(50) 23(50)
Mother BMI
< 18.5 6(75) 2(25)
18.5-24.9 68(48.6) 72(51.4) 0.288
25-29.9 50(52.6) 45(47.4)
> 30 14(40) 21(60)
pregnancy ranks
1 72(47.4) 72(48.6)
2 50(32.9) 47(31.8) 0.972
>2 30(19.7) 29(19.6)
type of delivery
NVD 30 (43.5) 39(56.5)
Caesarean 122(52.8) 109(47.2) 0.173
the history of abortions or stillbirths
Yes 34(22.4) 32(21.6)
No 118(77.6) 116(78.4) 0.876
infant sex
Female 75(48.7) 79(51.3)
Male 76(52.8) 68(47.2) 0.482
Mother occupational status
Employment 134(51.5) 126(48.5)
Housekeepers 18(45) 22(55) 0.441
Education level of mother
Under diploma 40(62.5) 24(37.5)
Diploma and more 112(47.5) 124(52.5) 0.033
Iron supplementation During pregnancy
Yes 120(48.2) 32(62.7) 129(51.8)19(37.3) 0.058
No
Iron supplementation after pregnancy
Yes 53(37.3) 99(62.7) 89(62.7) 59(37.3) < 0.001
No
*

Chi-square test.

The prevalence of pica was 11.8% in depressed women, and 4.7% in non-depressed women (P=0.026, OR=2.7), which meant that women with pregnancy pica were 2.7 times more likely to be affected by PPD (table 2). Sixty-four percent of women were reported practicing pica regularly on daily basis and Pagophagia (ice and freezer frost) was the most common non-food substance (76%, n=19) followed by Rosary and praying clay (24%, n=6). 64% of women experienced pica daily and Pica was most prevalent (84%, n=21) in the first trimester followed by 12% (n=3) and 4% (n=1) in the second and third trimester respectively. Ten women (40%) had no reason for pica, but 4 (16%) had severe craving, 1 (4%) wanted to reduce nausea, 8 (32%) wanted to reduce stress and anxiety, and 2 (8%) expressed other reasons. Women who practiced long term pica during pregnancy, were more prone to PPD (P=0.023), and all women with rosary and praying clay picas (n=6) were affected by PPD (P=0.024) (table 3). The results of study showed a significant association between regular iron supplementation during pregnancy and pica practice (P< 0.001) (Table 4), also there were significant association between postpartum iron supplementation with PPD (P< 0.001). Iron supplementation during pregnancy also had protective effect against PPD but wasn’t statistically significant (p=0.058) (Table 1).

Table 2.

The association between PPD and Pica during pregnancy

groups Pica during pregnancy Total P-value* OR** (95% CI***)

No Yes
N (%) N (%) N (%)
Non-depressed 141(95.3) 7(4.7) 148(100)
Depressed 134(88.2) 18(11.8) 152(100) 0.026 2.70 (1.095-6.685)
Total 275(91.7) 25(8.3) 300(100)
*

Chi-square test;

**

OR = odds ratio;

***

CI =confidence interval.

Table 3.

The association between Length and kind of pregnancy Pica with PPD

Variables Length of Pica during pregnancy (month) Type of pica
(%)N (%)N
0 ≥2 > 2 Nothing Ice and Freezer frost Rosary and praying clay
Depressed 134(48.7) 2(40) 16(80) 134(48.7) 12(63.2) 6(100)
Non-depressed 141(51.3) 3(60) 4(20) 141(51.3) 7(36.8) 0
Total 275(100) 5(100) 20(100) 275(100) 19(100) 6(100)
P-value* 0.023 0.024

Table 4.

The association between iron supplementation during pregnancy and pica practice

Variables Pica practice P-value*

No Yes Total
N (%) N (%) N (%)
Iron supplementation during pregnancy
Yes 237(95.2) 12(4.8) 249(100) P< 0.001
No 38(74.5) 13(25.5) 51(100)
*

Chi-square test.

By adjusting the confounding factors affecting depression in logistic regression, only iron supplementation after pregnancy was significant (Table 5).

Table 5.

Final logistic regression model for predicting PPD

variables P-value OR* 95 % C.I**
Lower Upper
Maternal education 0.201 1.485 0.81 2.723
Pica during pregnancy 0.153 2.043 0.767 5.438
Iron supplementation during pregnancy 0.822 1.084 0.536 2.191
Iron supplementation after pregnancy < 0.001 2.705 1.628 4.496

Note. Table is based on results of binary logistic regression (only for significant situations based on chi-square Test on Table 1).

*

Odds ratio

**

Confidence Interval.

4. Discussion

PPD is a common and multi factorial psychiatric disorder with biological, psychological, and sociological aspects interacting with mothers risk individually (Klainin & Arthur, 2009; Sooki et al., 2012). According to the various studies, women whit eating disorder such as anorexia nervosa and bulimia are exposed to different complications, including PPD (Leddy et al., 2009; Mazzeo et al., 2006; Meltzer-Brody et al., 2011). In this study, we assessed another form of eating disorder known as pica. The results of study showed that women who practiced pica during pregnancy, were more likely to PPD but by adjusting in logestic regression, it wasn’t statistically significant. There are very few studies on the association between pregnancy pica and PPD, and since the prevalence of pica is high in some African countries and Latin America (López & Langini, 2007; Nyaruhucha, 2009), more studies may be helpful.

Stress and anxiety is known as a risk factor for pica behavior in some studies. In case control study, an adult female patient ingested chalk in stressful situation (Bhatia & Gupta, 2009). Stressful life events also identified as an important predictors of PPD (Robertson, Grace, Wallington, & Stewart, 2004). We didn’t assess women Stress and anxiety during pregnancy but 32% (table 6) of women declared that pica reduced their stress and anxiety during pregnancy and all of them practiced PPD. We conclude that maybe Stress and anxiety during pregnancy is a cause of pica practice during pregnancy and PPD after delivery.

Table 6.

Frequency of Pica reasons by women in depressed and non-depressed groups

groups Pica reasons by women N (%)

Unable to say satisfy craving Relief of nausea reduced stress and anxiety Other reasons
Non-depressed 4 (40) 1(25) 1(100) 0(0) 1(50)
depressed 6(60) 3(75) 0 8(100) 1(50)
Total 10(100) 4(100) 1(100) 8(100) 2(100)

Anemia is known as important risk factors for pica behavior (Khoushabi et al., 2014; Rezavand & Rawshani, 2006; Saunders et al., 2009; Young et al., 2010). In some studies, there were also significant association between Anemia and PPD (Beard et al., 2005; Goshtasebi, Alizadeh, & Gandevani, 2013). In this study, pregnancy and postpartum anemia not assessed but the results of study showed a significant association between iron supplementation during pregnancy and pica practice. Iron supplementation during and postpartum also had a protective effect against PPD. In systematic Reviews, Iron supplements aimed at preventing PPD (Miller, Murray, Beckmann, Kent, & Macfarlane, 2013). A hypothesis about the association between PPD and pregnancy pica may related to anemia that manifest itself as a pica during pregnancy and PPD after delivery. So suggested that future studies assess anemia during and postpartum pregnancy when evaluate this association.

Limitation and Conclusions

In the present study, we tried to limit and match some confounding variables in assessing the relationship between PPD and pregnancy pica. So, recommended that future studies be conducted longitudinally and neutralization of other variables.

In this study, there wasn’t significant association between PPD and pica practice. In others studies, the association between another forms of eating disorders examined but pica practice not well studied. Given the importance of the subject on the individual and the community, further studies in this area are recommended.

In the present study, iron supplementation during and postpartum were an important factor against pica practice and PPD. Although iron supplementation for pregnant women is free in Iranian health care centers but some women don’t take iron supplements. Health practitioners should justify pregnant women about importance of taking supplements. In this study, pregnancy pica assessed 3-8 month after delivery so, maybe the prevalence of pica have been underestimated because of forgetfulness. Also, there are other variables may affect incidence of postpartum depression.

Footnotes

Conflict of Interest

Authors have no conflict of interests.

References

  1. Alipour Z, Lamyian M, Hajizadeh E. Sleep Quality in Late Pregnancy and Postpartum Depression. The Iranian Journal of Obstetrics Gynecology and Infertility. 2012;14(8):39–47. in persian. http://dx.doi.org/10.1016/j.ijgo.2012.02.004 . [Google Scholar]
  2. Beard J. L, Hendricks M. K, Perez E. M, Murray-Kolb L. E, Berg A, Vernon-Feagans L, Tomlinson M. Maternal iron deficiency anemia affects postpartum emotions and cognition. The Journal of Nutrition. 2005;135(2):267–272. doi: 10.1093/jn/135.2.267. http://www.ncbi.nlm.nih.gov/pubmed/15671224 . [DOI] [PubMed] [Google Scholar]
  3. Bhatia M. S, Gupta R. Pica responding to SSRI: an OCD spectrum disorder? The World Journal of Biological Psychiatry. The Official Journal of the World Federation of Societies of Biological Psychiatry. 2009;10(4 Pt 3):936–938. doi: 10.1080/15622970701308389. http://dx.doi.org/10.1080/15622970701308389 . [DOI] [PubMed] [Google Scholar]
  4. Boatin A, Wylie B, Singh M. P, Singh N, Yeboah-Antwi K, Hamer D. Prevalence of and risk factors for pica among pregnant women in Chhattisgarh, India. American Journal of Obstetrics & Gynecology. 2012;206(1):S299. http://dx.doi.org/10.1016/j.ajog.2011.10.689 . [Google Scholar]
  5. Field T. Postpartum depression effects on early interactions, parenting, and safety practices: a review. Infant Behavior & Development. 2010;33(1):1–6. doi: 10.1016/j.infbeh.2009.10.005. http://dx.doi.org/10.1016/j.infbeh.2009.10.005 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Goshtasebi A, Alizadeh M, Gandevani S. B. Association between Maternal Anaemia and Postpartum Depression in an Urban Sample of Pregnant Women in Iran. Journal of Health, Population, and Nutrition. 2013;31(3):398–402. doi: 10.3329/jhpn.v31i3.16832. Retrieved from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805890/ [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Grotegut C. A, Dandolu V, Katari S, Whiteman V. E, Geifman-Holtzman O, Teitelman M. Baking soda pica: a case of hypokalemic metabolic alkalosis and rhabdomyolysis in pregnancy. Obstetrics and Gynecology. 2006;107(2 Pt 2):484–486. doi: 10.1097/01.AOG.0000203666.99256.ed. http://dx.doi.org/10.1097/01.AOG.0000203666.99256.ed . [DOI] [PubMed] [Google Scholar]
  8. Janbabai G, Azadeh H, Farazmandfar T, Sayadi S, Sharifian R, Taghipour M. The Prevalence of Pica and the Associated Factors in Women with Iron Deficiency Anemia. Journal of Mazandaran University of Medical Sciences. 2011;21(85):21–26. [Google Scholar]
  9. Khoushabi F, Ahmadi P, Shadan M. R, Heydari A, Miri A, Jamnejad M. Pica Practices among Pregnant Women Are Associated with Lower Hemoglobin Levels and Pregnancy Outcome. Open Journal of Obstetrics and Gynecology. 2014;04(11):646–652. http://dx.doi.org/10.4236/ojog.2014.411090 . [Google Scholar]
  10. Klainin P, Arthur D. G. Postpartum depression in Asian cultures: a literature review. International Journal of Nursing Studies. 2009;46(10):1355–1373. doi: 10.1016/j.ijnurstu.2009.02.012. http://dx.doi.org/10.1016/j.ijnurstu.2009.02.012 . [DOI] [PubMed] [Google Scholar]
  11. Leddy M. A, Jones C, Morgan M. A, Schulkin J. Eating disorders and obstetric-gynecologic care. Journal of Women's Health (2002) 2009;18(9):1395–1401. doi: 10.1089/jwh.2008.1183. http://dx.doi.org/10.1089/jwh.2008.1183 . [DOI] [PubMed] [Google Scholar]
  12. Leung B. M. Y, Kaplan B. J. Perinatal depression: prevalence, risks, and the nutrition link--a review of the literature. Journal of the American Dietetic Association. 2009;109(9):1566–1575. doi: 10.1016/j.jada.2009.06.368. http://dx.doi.org/10.1016/j.jada.2009.06.368 . [DOI] [PubMed] [Google Scholar]
  13. López L. B, Langini S. H. Maternal iron status and neonatal outcomes in women with pica during pregnancy. International Journal of Gynaecology and Obstetrics: The Official Organ of the International Federation of Gynaecology and Obstetrics. 2007;98(2):151–2. doi: 10.1016/j.ijgo.2007.03.038. http://dx.doi.org/10.1016/j.ijgo.2007.03.038 . [DOI] [PubMed] [Google Scholar]
  14. Mazzeo S. E, Slof-Op't Landt M. C. T, Jones I, Mitchell K, Kendler K. S, Neale M. C, Bulik C. M. Associations among postpartum depression, eating disorders, and perfectionism in a population-based sample of adult women. The International Journal of Eating Disorders. 2006;39(3):202–211. doi: 10.1002/eat.20243. http://dx.doi.org/10.1002/eat.20243 . [DOI] [PubMed] [Google Scholar]
  15. Meltzer-Brody S, Zerwas S, Leserman J, Holle A. V, Regis T, Bulik C. Eating Disorders and Trauma History in Women with Perinatal Depression. Journal of Women's Health. 2011;20(6):863–870. doi: 10.1089/jwh.2010.2360. http://dx.doi.org/10.1089/jwh.2010.2360 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Mensah F. O, Twumasi P, Amenawonyo X. K, Larbie C, Jnr A. K. B. Pica practice among pregnant women in the Kumasi metropolis of Ghana. International Health. 2010;2(4):282–286. doi: 10.1016/j.inhe.2010.09.004. http://dx.doi.org/10.1016/j.inhe.2010.09.004 . [DOI] [PubMed] [Google Scholar]
  17. Miller B. J, Murray L, Beckmann M. M, Kent T, Macfarlane B. Dietary supplements for preventing postnatal depression. The Cochrane Database of Systematic Reviews. 2013;10:CD009104. doi: 10.1002/14651858.CD009104.pub2. http://dx.doi.org/10.1002/14651858.CD009104.pub2 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Mortazavi Z, Mohammadi M. Prevalence of pica in pregnant women referred to health care centers in Zahedan, Iran (2002-2003) African Journal of Food Science. 2010;4(10):642–645. [Google Scholar]
  19. Nyaruhucha C. N. M. Food cravings, aversions and pica among pregnant women in Dar es Salaam, Tanzania. Tanzania Journal of Health Research. 2009;11(1):29–34. [PubMed] [Google Scholar]
  20. Rezavand N, Rawshani D. Pica its Related Iron Deficiency Anaemia in Pregnant Women. Journal of Kermanshah University of Medical Sciences. 2006;10(3):226–234. in persian. [Google Scholar]
  21. Robertson E, Grace S, Wallington T, Stewart D. E. Antenatal risk factors for postpartum depression: a synthesis of recent literature. General Hospital Psychiatry. 2004;26(4):289–295. doi: 10.1016/j.genhosppsych.2004.02.006. http://dx.doi.org/10.1016/j.genhosppsych.2004.02.006 . [DOI] [PubMed] [Google Scholar]
  22. Sadock B. J, Sadock V. A. Kaplan & Sadock's Concise Textbook of Clinical Psychiatry. 10th ed. Vol. 26. Lippincott Williams & Wilkins; 2008. [Google Scholar]
  23. Saunders C, Padilha P, de Della C, Líbera B, Nogueira J. L, de Oliveira L. M, Astulla A. [Pica: epidemiology and association with pregnancy complications] Revista Brasileira De Ginecologia E Obstetrícia: Revista Da Federação Brasileira Das Sociedades De Ginecologia E Obstetrícia. 2009;31(9):440–446. doi: 10.1590/s0100-72032009000900004. [DOI] [PubMed] [Google Scholar]
  24. Sooki Z, Tagharobi Z, Sharifi S, Sharifi K, Musavi S, Zahmatkesh B. Predictors of Postpartum Depression in an Iranian Population, 2006. Nursing and Midwifery Studies. 2012;1(1):12–15. [Google Scholar]
  25. Thihalolipavan S, Candalla B. M, Ehrlich J. Examining pica in NYC pregnant women with elevated blood lead levels. Maternal and Child Health Journal. 2013;17(1):49–55. doi: 10.1007/s10995-012-0947-5. http://dx.doi.org/10.1007/s10995-012-0947-5 . [DOI] [PubMed] [Google Scholar]
  26. Young S. L, Khalfan S. S, Farag T. H, Kavle J. A, Ali S. M, Hajji H, Stoltzfus R. J. Association of Pica with Anemia and Gastrointestinal Distress among Pregnant Women in Zanzibar, Tanzania. The American Journal of Tropical Medicine and Hygiene. 2010;83(1):144–151. doi: 10.4269/ajtmh.2010.09-0442. http://dx.doi.org/10.4269/ajtmh.2010.09-0442 . [DOI] [PMC free article] [PubMed] [Google Scholar]

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