Prepregnancy Body Mass Index, Gestational Weight Gain, and the Likelihood of Major Depressive Disorder During Pregnancy
Objective: We assessed the relation between prepregnancy body mass index (BMI) and the likelihood of major depressive disorder (MDD) during pregnancy and tested whether this association was modified by gestational weight gain.
Method: Women (N = 242) were enrolled at < 20 weeks gestation into a prospective cohort study. Diagnosis of MDD was made with the Structured Clinical Interview for DSM-IV at 20, 30, and 36 weeks gestation. Gestational weight gain was compared with the 1990 Institute of Medicine weight gain recommendations. To assess the independent association between prepregnancy BMI and the odds of MDD, MDD at each time point was used as the dependent measure in a multivariable longitudinal logistic regression model employing generalized estimating equations. The data were collected from 2003–2007.
Results: There was a strong, positive dose- response association between prepregnancy BMI and the likelihood of MDD (P = .002). Compared with a BMI of 18, the adjusted odds ratios (95% confidence interval) for BMIs of 23, 28, and 33 were 1.4 (1.1 to 1.7), 1.9 (1.3 to 2.9), and 2.6 (1.4 to 4.3), respectively. Gestational weight gain significantly modified this effect. Among women with weight gains within and above the 1990 Institute of Medicine recommendations, pregravid overweight was associated with a greater likelihood of MDD. In contrast, all women with weight gains below recommended levels had an elevated odds of depression regardless of their pregravid BMI (P < .05).
Conclusions: Because pregravid overweight, poor gestational weight gain, and MDD all pose substantial risks for fetal development and birth outcomes, health care providers should monitor depression levels in these women to facilitate appropriate depression intervention.
J Clin Psychiatry 2009;70(9):1290–1296
© Copyright 2009 Physicians Postgraduate Press, Inc.
Submitted: August 27, 2008; accepted January 28, 2009.
Online ahead of print: July 14, 2009 (doi:10.4088/JCP.08m04651).
Corresponding author: Lisa M. Bodnar, PhD, MPH, RD, Department of Epidemiology, University of Pittsburgh, A742 Crabtree Hall, 130 DeSoto Street, Pittsburgh, PA 15261 (firstname.lastname@example.org).
In US women, obesity is a substantial and escalating health problem. It is the second leading cause of preventable death1 and dramatically increases morbidity associated with many chronic diseases.2 Nearly 2 of 3 adult women are classified as overweight (body mass index [BMI] > 25 kg/m2) and 1 in 3 is obese (BMI > 30 kg/m2).3 Over the past 30 years, the prevalence of obesity in women aged 20 to 74 years has doubled.4
Not surprisingly, more women are entering pregnancy overweight. It is estimated that 1 in 5 US women is overweight at the start of pregnancy, a figure that has risen 70% in the last decade.5 Obesity during pregnancy poses unique risks to the mother and fetus. High maternal prepregnancy BMI has been linked with countless adverse perinatal outcomes, including preeclampsia, miscarriage, congenital malformations, stillbirth, neonatal death, gestational diabetes, operative delivery, and infant macrosomia.6 Little is known about the consequences of prepregnancy obesity on maternal mental health outcomes, including major depressive disorder (MDD). Moreover, the effect of MDD on the development of obesity has also been underexplored.
Research in nonpregnant adults indicates that obesity is associated with depressive symptoms,7,8 lifetime diagnosis of major depression,9 and history of depression.10 Moreover, obesity has been shown to not only predict the onset of major depression,11,12 but also result from major depression.13–15 There is some suggestion that the positive association between obesity and depression is stronger in women than in men.16,17 Whether these findings can be generalized to pregnant women remains largely unknown.
Pregnancy is a unique developmental stage involving weight gain. Thus, the association between weight and mood must be viewed in the context of a woman’s prepregnancy weight as well as her gestational weight gain. Adequate weight gain is necessary for the growth and development of maternal and fetal tissues.18 Consequently, women may positively attribute weight at conception and gestational weight gain to ensuring the health of the infant. Indeed, pregnancy is often accompanied by positive behavioral and attitudinal changes with regard to weight and nutrition,19 yet evidence suggests that negative weight gain attitudes and dissatisfaction with weight/shape may resurface as pregnancy advances.20,21 Because changes in appetite and body weight are among the diagnostic criteria for MDD, extremes of both prepregnancy BMI and total gestational weight gain may be markers of antenatal depression. An understanding of the interaction between prepregnancy weight and gestational weight gain on antenatal depression may help to identify high-risk groups that will benefit from depression screening and intervention.
Our objectives were 2-fold. First, we sought to assess the relation between prepregnancy BMI and the likelihood of MDD during pregnancy. Second, we tested whether this association was modified by gestational weight gain. We hypothesized that pregravid overweight was associated with antenatal MDD regardless of gestational weight gain and that lean women with inadequate and excessive weight gain also had a higher prevalence of depression.
Data were obtained from the Antidepressant Use During Pregnancy Study, an observational cohort study designed to investigate the effects of maternal depression and antidepressant use on pregnancy outcomes and childhood development.22 Data were collected from 2003–2007. Women with or without MDD and/or antidepressant use in the index pregnancy were invited to enroll at < 20 weeks gestation. We did not separate the exposures on the basis of whether the depressive episode during the pregnancy was the first episode or recurrent. Recruitment was by self-referral and physician referral, advertising, and screening in the obstetrical ultrasound suite. Consultation about depression management during pregnancy was provided to women with depression or antidepressant exposure, and a summary was sent to the woman and her physician(s). Enrollment did not depend upon acceptance of recommendations or treatment choice. No intervention was prescribed by the study team.
Women were excluded if they had psychosis, bipolar disorder, active substance use disorder (identified by self-report or urine drug screen), gestational exposure to benzodiazepines or prescription drugs in the US Food and Drug Administration–defined category of D or X23 (other than selective serotonin reuptake inhibitors [SSRIs]), a multifetal gestation, or a pregestational chronic disease. Study visits occurred at approximately 20, 30, and 36 weeks’ gestation. At baseline, data on sociodemographic characteristics, health behaviors, medication exposures, and prepregnancy weight were collected via interview, and maternal height was measured. At each study visit, maternal depression was assessed by an experienced, trained clinician (see Definition of Study Variables) and maternal weight was measured. Approval was obtained from the University of Pittsburgh Institutional Review Board, and all women provided informed, written consent.
A total of 251 eligible women enrolled in the study. We excluded women who lacked data on prepregnancy weight or height (n = 1) or covariates in our final model (n = 2). One woman was excluded because she was too heavy to be weighed on the study scale. We also excluded 5 observations that represented a second pregnancy to the same woman. The final analytic sample included 242 women. Of these women, 71.1% had depression assessments at all 3 pregnancy study visits, while a smaller proportion had depression data available at 1 (15.7%) or 2 (13.2%) visits only. Therefore, a total of 624 person-observations were included in the prepregnancy BMI analysis. Gestational weight measurements at each study visit were missing for some women, so the sample size for the analyses involving gestational weight gain was reduced to 239 women contributing 552 person-observations.
Definition of Study Variables
At each visit, the diagnosis of MDD was made according to the Structured Clinical Interview for DSM-IV (SCID)24 by an experienced, trained clinician. We adapted the timeline technique25 to chart MDD course by month across pregnancy.26 Depression severity was assessed with the 29-item Structured Interview Guide for the Hamilton Depression Rating Scale-Atypical Depression Symptoms Version (SIGH-ADS),27 which includes all versions of the Hamilton Rating Scale for Depression.28
Prepregnancy BMI (weight [kg]/height [m]2) was based on measured height and maternal self-report of prepregnancy weight at enrollment. Body mass index was categorized as underweight (BMI < 18.5), normal weight (BMI = 18.5–24.9), overweight (BMI = 25.0–29.9), and obese (BMI ≥ 30.0).29 Gestational weight gain at each visit was calculated by subtracting the prepregnancy weight from the measured weight. Gestational weight gain was compared with the prepregnancy BMI-specific 1990 Institute of Medicine (IOM) weight gain recommendations.18 Each woman’s actual observed weight gain was divided by her expected weight gain at the gestational age that corresponded with each study visit.18 Weight gain was classified as below the lower cut-off of 1990 IOM recommendations, within the IOM–recommended range, or above the upper cut-off of recommendations as we have done in previous analyses.30
Maternal ethnicity/race was based on self-report. Data on maternal age, parity (primiparous, multiparous), smoking status (smoker or nonsmoker), education (less than high school, high school or equivalent, or some college), marital status (married or unmarried), and work status (full-time, part-time, or none) were also available. Gestational age was determined by maternal report of the date of the last menstrual period and was confirmed with ultrasound when available. Self-reported SSRI use at each visit was verified using serum concentrations.
To assess the independent association between prepregnancy BMI and the odds of depression, depression status at each time point during the index pregnancy was used as the dependent measure in a longitudinal logistic-regression model employing generalized estimating equations, which account for intraindividual correlation of depression measurements.31 To assess the dose-response relation between BMI and depression, we used published methods32 to determine the most appropriate specification of BMI in our models. We tested numerous spline terms and fractional polynomials, but the best fit was found using BMI as a continuous, linear variable in all models.
We fit parsimonious regression models by specifying full models with potential confounding variables: race/ethnicity, maternal age, height, education, marital status, work status, parity, smoking status, SSRI use, and gestational age at study visit. Effect modification by gestational weight gain, race/ethnicity, SSRI use, and study visit was tested using Wald P values (α = .10) and examining stratum-specific results. Potential confounders were considered to not be influential and were removed from the model if their inclusion did not satisfy our a priori criteria: a change of the main-effect odds ratio (OR) by ≥ 10%. Study visit gestational age was included in all models regardless of its effect on the point estimates. Maternal education met our definition of confounding in the final BMI model, and education and work status met our definition of confounding in the BMI–weight gain model.
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Most of the 242 women in the study were white, aged 26 to 30 years, college-educated, married, and nonsmokers and had at least 1 previous live birth (Table 1). Nearly half of the sample was overweight or obese at the start of pregnancy. At baseline, approximately 25% of women had a diagnosis of MDD and 20% were taking SSRIs for treatment of depression. Mean (SD) depressive symptom scores using the 29-item SIGH-ADS were 9.2 (5.4) among women without a diagnosis of current MDD and 21.9 (4.7) among women diagnosed with MDD at enrollment. Women in the SSRI-treated groups had the expected therapeutic benefit, that is, they had less depression than the women in the depression group not treated with SSRIs (data not shown).
The prevalence of MDD varied significantly across prepregnancy BMI categories (Table 2). Depression was least common in normal-weight women and increased in prevalence among overweight and obese women. Estimates were imprecise for underweight women due to the small sample size. After adjustment for education and visit gestational age, the ORs (95% CIs) for MDD compared with normal-weight women were 2.3 (0.5 to 11.1) for underweight women, 1.7 (0.9 to 3.4) for overweight women, and 2.9 (1.5 to 5.6) for obese women.
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There was a strong, positive dose-response association between prepregnancy BMI and the likelihood of MDD (Figure 1, P = .002). Compared with women who had a BMI of 18, the odds of depression among women with a BMI of 28 and 33 were 1.9-fold and 2.6-fold higher, respectively, after confounder adjustment (Table 3). Importantly, even normal-weight women with a BMI of 23 had a 40% increased adjusted odds of MDD when compared with the same referent. There was no evidence that this effect varied by race/ethnicity, gestational age at study visit, or SSRI use.
More than half of the women gained above the BMI- specific 1990 IOM–recommended weight gain ranges at weeks 20 (53.2%), 30 (57.5%), and 36 (60.3%), with the remaining women gaining below or within recommended ranges. Low weight gain was more common than weight gains within the recommended ranges at 20 weeks (30.4% vs 16.5%) and 30 weeks (24.7% vs 17.8%). At 36 weeks, 23.4% of women gained within the IOM–recommended range, while 16.3% gained below the recommended range.
Gestational weight gain significantly modified the effect of prepregnancy BMI on the likelihood of MDD (Figure 2, P = .01 for interaction). Among women with weight gain less than the 1990 IOM recommendations, there was no association between prepregnancy BMI and the odds of depression independent of work status, education, and gestational age at study visit. Women who gained below the 1990 IOM recommendations were about 3.5 times as likely to have antenatal depression as lean women with adequate weight gain, regardless of their pregravid BMI (P < .05). In contrast, among women who gained within the 1990 IOM weight gain range, there was a strong, positive linear relation between pregravid BMI and depression. Each 5-unit increase in BMI was associated with a 2.4-fold (95% CI = 1.4 to 4.1) increase in the likelihood of MDD after confounder adjustment. This association was slightly attenuated in women who gained above the 1990 IOM recommendations. Women who gained above the IOM recommendations and whose BMI values were 28 or more had a significant increase in the adjusted odds of depression compared with lean women gaining within the recommended range (eg, Oregon Scientific BMI scale, Sydney, Australia, OR [95% CI] for BMI 28: 3.2 [1.2 to 8.1]; BMI 33: 4.9 [1.8 to 13.4]). This association was not further modified by race/ethnicity or gestational age at study visit.
None of the results changed meaningfully when we restricted analyses to women who contributed data to all 3 study visits or further adjusted for maternal age, height, race/ethnicity, marital status, SSRI use, and smoking status (data not shown).
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We observed a strong, linear dose-response relationship between prepregnancy BMI and the likelihood of antenatal MDD that remained after controlling for measured confounders. When we studied how this effect varied by gestational weight gain, we found that high pregravid BMI was associated with MDD among women who gained within and above the 1990 IOM–recommended ranges. In the subgroup of women with gestational gain below the 1990 IOM–recommended ranges, depression was prevalent among all women, regardless of their prepregnancy BMI. To our knowledge, ours is the first study to explore the joint effects of prepregnancy BMI and gestational weight gain on the likelihood of antenatal depression.
Our results relating an increasing BMI to a greater odds of MDD are consistent with the growing body of evidence of a positive association between obesity and depression in adults.7–17 Importantly, as with another investigation,11 we found an increasing likelihood of depression across the linear range of BMI values, such that even small increases within the range of “normal weight” were associated with a higher likelihood of MDD. Few investigators have rigorously explored the association between weight and depression in the context of pregnancy.
In a cross-sectional analysis, Cameron and colleagues33 studied 132 low-income women and found that having a body weight that deviated substantially from the recommended weight in the third trimester was associated with a higher depressive symptom score among white women with low self-esteem. Among white women with high self-esteem, high weight deviations were negatively associated with depressive symptoms. Interestingly, weight deviation was not related to depression among the 36 black women studied. While these findings are intriguing, the authors’ method of characterizing weight prevents the disentanglement of prepregnancy weight from gestational weight gain.
Our results contradict those of Carter and colleagues,19 who reported no correlation between prepregnancy BMI and depressive symptom scores between the fifth and eighth month of pregnancy in 64 middle-class women. However, their results were limited by a reliance on depressive symptom scores rather than psychiatric diagnostic criteria, women’s self-reporting of pregravid weight at 4 months postpartum, lack of data on gestational weight gain, and failure to adjust for confounding variables.19 Prepregnancy obesity was associated with prevalent postpartum depression in 2 studies,19,34 but neither explored the potential modifying effects of gestational weight gain.
In our study, women who entered pregnancy overweight had a high likelihood of MDD regardless of whether they gained gestational weight below, within, or above the 1990 IOM–recommended ranges. Therefore, overweight mothers’ antenatal mood may be unaffected by the amount of weight gained and, rather, more strongly associated with weight at conception. The mechanisms underlying the overweight-depression relation are uncertain but likely involve psychological, sociological, biologic, and behavioral factors.35,36 If obesity precedes depression, the extreme value placed on slimness in today’s society may cause obese women to feel stigmatized and to suffer from body-image dissatisfaction leading to chronic depression that may predate the pregnancy.37 Indeed, comorbid conditions related to weight, such as anxiety and/or eating disorders, may partially mediate this association. Furthermore, unhealthy behaviors common to overweight individuals, such as physical inactivity and poor dietary quality, may also adversely affect mood.38,39 Overweight women are more likely to experience pregnancy complications,6 which may be stressful and increase the likelihood of depressive symptoms. Biologic factors such as circulating leptin concentrations may be relevant. Leptin inhibits depressive symptoms in animal models, so the leptin resistance that characterizes obesity may contribute to obese individuals’ higher prevalence of depression.40
It is crucial to underscore that although prospective studies have shown that obesity predicts the onset of major depression,11,12 the causal pathway may be reversed. Preconception depression may cause obesity in some women, as has been illustrated in several studies of nonpregnant women.13–15 Alternatively, depression and obesity may share the same underlying pathophysiology and be manifestations of the same disease.41,42 Unfortunately, we lacked data on pregravid mood and pregravid SSRI use, thereby preventing us from exploring the temporality of the association between prepregnancy BMI and depression in our population. Because it is plausible that the causal pathway goes in either direction between weight and depression, it is imperative that longitudinal data are collected in future studies to clarify the temporality of this relation.
We also observed that lean women who gained below the 1990 IOM–recommended range had an elevated odds of MDD, which is consistent with previous work. Hickey et al43 conducted a prospective study of depressive symptoms at 24–26 weeks and inadequate gestational weight gain in a large cohort of low-income, nonobese black and white women. The authors reported that white women in the highest quartile of depressive symptom score were 3.0 (95% CI = 1.2 to 6.2) times as likely as women in the lowest quartile to have weight gain below the 1990 IOM–recommended range.43 No relationship was found between depression and low weight gain in black women.43
In a cohort of over 4,000 Hispanic women, self-reported feelings of depression during pregnancy were negatively associated with pregnancy weight gain in univariate models, but this variable was no longer significant once other psychosocial factors and maternal characteristics were considered.44 In cross-sectional studies, high depressive symptoms have been linked with negative attitudes about gaining gestational weight.21,45 Collectively, these findings indicate that weight gain below the 1990 IOM–recommended range may be a marker of depression during pregnancy.
Few investigators have explored depression as it relates to gestational weight gain in excess of national recommendations. In a recent study, pregnant women who gained in excess of the 1990 IOM recommendations were more likely to have high depressive symptoms than women who met the weight gain recommendations.46 In contrast, we found that lean women who gained above the 1990 IOM–recommended range were not more likely than lean women who gained within the recommended range to be depressed during pregnancy. We also reported that the association between pregravid BMI and MDD was slightly attenuated among those who gained excessive weight. Because the confidence intervals among adequate and excessive weight gainers at the same BMI value substantially overlaped (Figure 2), it is difficult to discern if this is a true finding. However, it is possible that women who gain within the IOM-recommended range are more weight conscious than women who gain more than recommended, and that pregravid obesity in this group would be associated with more psychological distress.
Our study was limited by a lack of data on body image, weight/shape satisfaction, and weight gain attitudes, which may modify the associations we observed. Prepregnancy BMI and gestational weight gain were both calculated on the basis of maternal self-report of pregravid weight. Because women tend to underreport their weight,47 BMI may have been underestimated and weight gain overestimated. Whether such misreporting varies by depression status, and thus would lead to differential misclassification, is not known.
Although we found no evidence that the associations between weight and depression varied by race/ethnicity, we had a relatively small sample of black women (n = 40) and therefore limited power to detect 2- and 3-way interactions among BMI, weight gain, and race. Additionally, because < 3% of our population had a pregravid BMI < 18.5 kg/m2, we were unable to determine with confidence the likelihood of MDD among underweight women. Unmeasured confounding by factors like comorbid psychiatric conditions, prepregnancy dietary intake and physical activity, prepregnancy access to health care, and/or maternal genetic factors predisposing to obesity and depression may have biased our results, and confounders we did collect may have been measured with error.
In the future, large, racially diverse cohorts with wide ranges of BMI and weight gains and data on preconception mood and SSRI use, attitudes about weight, and health behaviors are needed to overcome these limitations. Our cohort had a high risk of MDD, and additional studies are needed to determine whether or not our findings are generalizable to a broader population of pregnant women.
Our results suggest that MDD during pregnancy is prevalent among women who have gestational weight gains below the 1990 IOM–recommended range and increases in prevalence as prepregnancy BMI increases. These findings signify an important public health problem, as obesity has reached epidemic proportions3 and low weight gain occurs commonly.48 Future studies must clarify the temporality of the complex relation between pregravid weight, weight gain, and depression in pregnant women. Because maternal overweight, poor weight gain, and MDD all pose substantial risks for fetal development and birth outcomes,6,18,49 it is critical that health care providers monitor depression levels of obese pregnant women and women with weight gains below the 1990 IOM–recommended range in order to facilitate appropriate depression intervention.
Author affiliations: Department of Epidemiology, University of Pittsburgh Graduate School of Public Health (Drs Bodnar and Wisner); Department of Psychiatry (Drs Bodnar, Wisner, Moses-Kolko, Sit, and Hanusa) and Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine (Drs Bodnar and Wisner); and Women’s Behavioral HealthCARE (Drs Wisner, Moses-Kolko, Sit, and Hanusa), Pittsburgh, Pennsylvania.
Financial disclosure: Dr Wisner has received funding from the National Institute of Mental Health, the Stanley Medical Research Foundation, the American Society for Bariatric Surgery, New York-Mid-Atlantic Consortium for Genetic and Newborn Screening Services, the state of Pennsylvania, Wyeth, the Heinz Foundation, and Pfizer and serves on the speaker’s bureau of GlaxoSmithKline. Drs Bodnar, Moses-Kolko, Sit, and Hanusa report no other financial affiliations relevant to the subject of this article.
Funding/support: This study was supported by National Institutes of Health/National Institute of Mental Health grants K01 MH074092 to Dr Bodnar and R01 MH060335 to Dr Wisner.
Previous presentation: Presented at the Annual Meeting of the Society for Maternal-Fetal Medicine, January 28–February 2, 2008, Dallas, Texas.
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