Background.

Latinas in the United States have elevated rates of diabetes and prenatal depression (PND). The presence of diabetes and PND can also have a negative effect on women’s self-rated health (SRH), a commonly used indicator of health that is consistent with objective health status and is a predictor of mortality. However, the associations between PND, diabetes, and SRH have not been tested, particularly among Latinas, who have elevated risk of both medical conditions. To address this gap, this pilot study tested the association between PND and diabetes using data from Latinas enrolled during their third trimester of pregnancy and explored whether these health conditions were associated with SRH in these women.

Methods.

For this study, the Edinburgh Postnatal Depression Scale was used to determine PND status, self-reported medical history to determine diabetes status, and SRH before and during the current pregnancy in a sample of 34 prenatal Latinas. Participants were invited to take part in the study in their third trimester of pregnancy. Bivariate analyses and logistic regressions were used to test associations between demographic variables, PND, diabetes, and SRH.

Results.

There was no significant association between PND and diabetes status in this sample of Latinas. There was a significant difference in SRH from pre-pregnancy to pregnancy, with worse ratings reported during pregnancy. Furthermore, women with PND or diabetes reported worse SRH, even after controlling for pre-pregnancy SRH.

Conclusion.

SRH is an important and robust variable associated with PND and diabetes in prenatal Latinas, making it an important factor to assess when treating this high-risk group.

The prevalence of diabetes in pregnancy (type 2 diabetes and gestational diabetes mellitus [GDM]) is growing in the United States and globally, making it an international public health priority (18). Women who develop GDM (i.e., glucose intolerance first detected during pregnancy [9]) are more than seven times as likely to develop type 2 diabetes than women who have had a normoglycemic pregnancy (10,11). Another complication in pregnancy is prenatal depression (PND), estimated to occur in 5% (12,13) to 51.4% (13,14) of the general population. Rates of these two medical complications are high among Latinas in the United States—an important fact because Latinas are the fastest-growing ethnic minority group (15), have the highest fertility rate in the United States (16), experience high rates of PND (32% [17]), and are at least twice as likely to develop diabetes in pregnancy than white women (1,18,19). Given the comorbidity of PND and diabetes in pregnancy among Latinas and their potential long-term effects on mother and child, it is imperative to further explore these two medical conditions in this population.

Several studies have found associations between diabetes in pregnancy and PND (2022). Examining PND in the context of diabetes (type 2 diabetes and GDM) is important because both conditions act as risks for postpartum mothers and their children (23). In mothers, both diabetes and PND are risk factors for postpartum mood disorders (21,2430). Depressive symptoms in mothers have been associated with poor overall health (31) and pregnancy complications (32,33). PND has also been associated with a host of negative outcomes for the child, including preterm birth (34,35), low birth weight (35), negative reactivity/affect (3639), sudden infant death syndrome (40), and developmental delay (41). Furthermore, women with diabetes in pregnancy are at increased risk for hypertensive disorders and are more likely to need cesarean delivery (42,43). These health risks are particularly important for Latinas, who have been shown to have increased risks of obesity (44) and preeclampsia (45), which have been associated with diabetes. Infants of women with diabetes in pregnancy, including pregestational diabetes, are at increased risk for fetal macrosomia (being large for gestational age), obesity, glucose intolerance, and diabetes later in life (42,4648). High rates of several of these infant risk factors, such as macrosomia (49) and child obesity (50), have been found in Latino offspring.

The presence of diabetes and PND can also have a negative effect on women’s self-rated health (SRH), a commonly used indicator of health that is consistent with objective health status (51,52) and is a predictor of mortality (53). Prior studies have also shown an association between poorer SRH during pregnancy and depressive symptoms (5456), as well as between poor SRH and diabetes in pregnancy (28,57). However, it is unclear how SRH is associated with PND and diabetes, particularly among Latinas who are diverse in countries of origin, nativity, immigration status, and acculturation. These factors are particularly important to examine given the complex stressors and risk factors immigrant (58) and more acculturated Latinas (59) experience.

Given the predictive role of SRH and the long-term implications of poor health in pregnancy for maternal and child outcomes, it is important to explore the effects of diabetes and PND on SRH in prenatal Latinas. Yet, these associations have not been well explored. To address this gap in the literature, we tested the association between diabetes and PND and explored whether SRH was associated with these two health conditions in a sample of 34 Latinas enrolled in their third trimester of pregnancy. Because the relationship between PND and diabetes may be moderated by key demographic characteristics, we also explored associations between immigrant status, age, education, income, marital status, employment, and our outcomes of interest. This work extends prior research conducted with Latinas (60,61) by exploring associations between two important perinatal health factors (e.g., diabetes and depression), maternal characteristics, and SRH.

We used data from SEPAH Latina (Study of Exposure to Stress, Postpartum Mood, Adverse Life Events, and Hormonal Function Among Latinas), which collected health information from 34 Latina women from their third trimester of pregnancy to 8 weeks postpartum between July 2013 and April 2014 (see Lara-Cinisomo et al. [62] for study details). The study was approved by the University of North Carolina Chapel Hill institutional review board. All participants gave written informed consent. Interviews were conducted in Spanish or English, and all women were compensated for their participation.

Measures

Demographic information, self-reported medical conditions, and medication use were collected at enrollment. Depression status was determined using the Edinburgh Postnatal Depression Scale (EPDS), a reliable measure of prenatal depressive symptoms (63); a score >10 indicated PND (64). The EPDS was validated with prenatal (65) and Spanish-speaking Latinas (66).

SRH was determined from answers to two social comparison questions in two time periods: “Compared to other people your age, how would you describe the state of your physical health during the year before your pregnancy?” or “Compared to other people your age, how would you describe the state of your physical health since you’ve been pregnant?” Responses were chosen from a five-point Likert scale (poor to excellent) (67).

Data Analysis

Participant characteristics were summarized using descriptive statistics. Using SPSS 23 (IBM, Armonk, N.Y.), Fisher exact tests were used to determine associations between dichotomous variables (e.g., education, diabetes status, and PND status), and χ2 tests determined associations between categorical variables (e.g., SRH and type of medication). Nonparametric tests for paired data determined differences in pre-pregnancy and pregnancy SRH. Binary logistic regressions were used to determine the effect of diabetes on PND. Ordinal logistic regressions were implemented to test associations between SRH during pregnancy (dependent variable) and diabetes status (e.g., any diabetes and GDM). We also controlled for PND, pre-pregnancy SRH, and demographic characteristics to determine the unique contributing effect of these variables. Only significant predictors were retained in the final model. An α level ≤0.05 was used to determine significant findings.

Table 1 summarizes descriptive statistics and shows that 26.5% of women reported a diagnosis of diabetes, 14.7% reporting a diagnosis of GDM, 76.7% were overweight or obese, and 32.4% had PND. Less than one-fourth (23.5%) rated their pre-pregnancy health as fair or poor, but this proportion nearly doubled during pregnancy (41.2%). Results show that SRH was significantly lower during pregnancy compared to pre-pregnancy (P = 0.022). No significant associations were found between demographic characteristics, diabetes status (any diabetes or GDM), any SRH, or PND.

TABLE 1.

Descriptive Statistics of Study Participants (n = 34)

Immigrant status  
 Immigrant 85.3 (29) 
 U.S.-born 14.7 (5) 
Marital status  
 Single 26.5 (9) 
 Married or cohabitating 73.5 (25) 
Education level  
 Less than high school 55.9 (19) 
 High school or more 44.1 (15) 
Employment  
 Unemployed 79.4 (27) 
 Employed full-time 20.6 (7) 
Annual household income  
 <$20,000 50.0 (17) 
 >$20,000 41.2 (14) 
 Did not know 08.8 (3) 
Diabetes diagnosis  
 Any type 26.5 (9) 
 None 73.5 (25 
 Gestational 14.7 (5) 
 Non-gestational 85.3 (29) 
Medication/vitamin use  
 Diabetes-related 23.5 (8) 
 Other medications or prenatal vitamins 47.0 (16) 
 None reported 23.5 (8) 
 Missing 5.9 (2) 
Prenatal depression status  
 Depressed 32.4 (11) 
 Not depressed 67.6 (23) 
BMI  
 Underweight or normal (BMI ≤24.9 kg/m223.3 (7) 
 Overweight or obese (BMI ≥25.0 kg/m276.7 (23) 
Pre-pregnancy self-rated health  
 Poor 0 (0) 
 Fair 23.5 (8) 
 Good 20.6 (7) 
 Very good 35.3 (12) 
 Excellent 20.6 (7) 
Pregnancy self-rated health  
 Poor 8.8 (3) 
 Fair 32.4 (11) 
 Good 17.6 (6) 
 Very good 20.6 (7) 
 Excellent 20.6 (7) 
Age (years), mean (SD) 29.3 (5.9) 
Immigrant status  
 Immigrant 85.3 (29) 
 U.S.-born 14.7 (5) 
Marital status  
 Single 26.5 (9) 
 Married or cohabitating 73.5 (25) 
Education level  
 Less than high school 55.9 (19) 
 High school or more 44.1 (15) 
Employment  
 Unemployed 79.4 (27) 
 Employed full-time 20.6 (7) 
Annual household income  
 <$20,000 50.0 (17) 
 >$20,000 41.2 (14) 
 Did not know 08.8 (3) 
Diabetes diagnosis  
 Any type 26.5 (9) 
 None 73.5 (25 
 Gestational 14.7 (5) 
 Non-gestational 85.3 (29) 
Medication/vitamin use  
 Diabetes-related 23.5 (8) 
 Other medications or prenatal vitamins 47.0 (16) 
 None reported 23.5 (8) 
 Missing 5.9 (2) 
Prenatal depression status  
 Depressed 32.4 (11) 
 Not depressed 67.6 (23) 
BMI  
 Underweight or normal (BMI ≤24.9 kg/m223.3 (7) 
 Overweight or obese (BMI ≥25.0 kg/m276.7 (23) 
Pre-pregnancy self-rated health  
 Poor 0 (0) 
 Fair 23.5 (8) 
 Good 20.6 (7) 
 Very good 35.3 (12) 
 Excellent 20.6 (7) 
Pregnancy self-rated health  
 Poor 8.8 (3) 
 Fair 32.4 (11) 
 Good 17.6 (6) 
 Very good 20.6 (7) 
 Excellent 20.6 (7) 
Age (years), mean (SD) 29.3 (5.9) 

Data are n (%) unless otherwise noted. BMI is based on 30 women. Four women were lost to follow-up and did not attend the laboratory visit where weight and height were recorded.

Among women with any type of diabetes (type 2 diabetes or GDM) during pregnancy, 33% had PND, but this proportion was higher among women with GDM (40%). Results from the logistic regression indicated that there was no significant association between any diabetes or GDM and PND (Table 2). Pregnancy SRH was significantly associated with PND [χ2 (df 4, n= 34) = 12.40, P = 0.015]. There were significant differences in pre-pregnancy [H(1) = 5.266, P = 0.022] and marginal differences in pregnancy [H(1) = 7.761, P = 0.055] SRH by PND status. There were also significant differences in pre-pregnancy [H(1) = 6.021, P = 0.014] and pregnancy [H(1) = 7.251, P = 0.007] SRH by any type of diabetes. Differences in pregnancy SRH by GDM status were also significantly different [H(1) = 4.317, P = 0.038]; pre-pregnancy ratings differed only marginally [H(1) = 2.780, P = 0.095].

TABLE 2.

Results From the Logistic Regressions for Diabetes Status by PND (n = 34)

Any DiabetesGDM Only
β (SE)95% CIPβ (SE)95% CIP
PND 0.061 (0.48) 0.21–5.37 0.942 0.393 (1.00) 0.21–10.46 0.693 
Any DiabetesGDM Only
β (SE)95% CIPβ (SE)95% CIP
PND 0.061 (0.48) 0.21–5.37 0.942 0.393 (1.00) 0.21–10.46 0.693 

Results from the ordinal logistic regressions indicated that there was a significant and negative association between any diabetes and pregnancy SRH (P = 0.008) (see Model 1, Table 3). GDM was also negatively associated with pregnancy SRH (P = 0.021) (see Model 1, Table 4). Given our interest in the association between diabetes status and pregnancy SRH, individual predictors were added to the primary model. Results revealed that PND was negatively associated with pregnancy SRH (P = 0.002); the effect of any diabetes on pregnancy SRH remained statistically significant (P = 0.002) (see Model 2, Table 3). Similar results were observed for GDM (see Model 2, Table 4). Adding pre-pregnancy SRH to the model testing the effect of diabetes (any diabetes or GDM) on pregnancy SRH rendered its effect nonsignificant (see Model 3, Tables 3 and 4); pre-pregnancy SRH ratings were significantly associated with pregnancy SRH. The final models in Tables 3 and 4 show that diabetes status was significantly and negatively associated with pregnancy SRH after controlling for PND and pre-pregnancy SRH, which was also statistically significant with the exception of “good” ratings in the any diabetes model. Demographic characteristics did not yield any significant effects.

TABLE 3.

Results From the Ordinal Logistic Regressions With Pregnancy SRH as the Outcome and Any Diabetes as the Main Predictor (n = 34)

Model 1Model 2Model 3Model 4
B (SE)95% CIPB (SE)95% CIPB (SE)95% CIPB (SE)95% CIP
Any diabetes –2.167 (0.82) –3.77 to –0.56 0.008 –2.638 (0.853) –4.31 to –0.97 0.002 –1.355 (0.85) –3.04 to 0.33 0.115 –2.301 (0.95) –4.15 to –0.45 0.015 
PND    –2.368 (0.78) –3.90 to –0.84 0.002    –2.323 (0.88) –4.05 to –0.59 0.008 
Pre-pregnancy SRH            
 Poor       — — — — — — 
 Fair       –4.994 (1.37) –7.68 to –2.31 0.000 –4.375 (1.42) –7.15 to –1.60 0.002 
 Good       –3.236 (1.24) –5.67 to –0.81 0.009 –2.309 (1.24) –4.74 to 0.12 0.062 
 Very good       –2.83 (1.06) –4.45 to –0.31 0.024 –2.499 (1.08) –4.61 to –0.39 0.020 
Model 1Model 2Model 3Model 4
B (SE)95% CIPB (SE)95% CIPB (SE)95% CIPB (SE)95% CIP
Any diabetes –2.167 (0.82) –3.77 to –0.56 0.008 –2.638 (0.853) –4.31 to –0.97 0.002 –1.355 (0.85) –3.04 to 0.33 0.115 –2.301 (0.95) –4.15 to –0.45 0.015 
PND    –2.368 (0.78) –3.90 to –0.84 0.002    –2.323 (0.88) –4.05 to –0.59 0.008 
Pre-pregnancy SRH            
 Poor       — — — — — — 
 Fair       –4.994 (1.37) –7.68 to –2.31 0.000 –4.375 (1.42) –7.15 to –1.60 0.002 
 Good       –3.236 (1.24) –5.67 to –0.81 0.009 –2.309 (1.24) –4.74 to 0.12 0.062 
 Very good       –2.83 (1.06) –4.45 to –0.31 0.024 –2.499 (1.08) –4.61 to –0.39 0.020 

The reference groups were no diabetes, no PND, and excellent SRH.

TABLE 4.

Results From the Ordinal Logistic Regressions With Pregnancy SRH as the Outcome and GDM as the Main Predictor (n = 34)

Model 1Model 2Model 3Model 4
B (SE)95% CIPB (SE)95% CIPB (SE)95% CIPB (SE)95% CIP
GDM only –2.383 (1.03) –4.91 to –0.36 0.021 –2.434 (1.03) –4.45 to –0.41 0.018 –1.825 (1.07) –7.85 to –2.64 0.087 –2.230 (1.11) –4.41 to –0.05 0.045 
PND    –2.016 (0.75) –3.49 to –0.54 0.007    –1.816 (0.84) –3.46 to –0.17 0.031 
Pre-pregnancy SRH            
 Poor       — — — — — — 
 Fair       –5.191 (1.36) –7.85 to –2.54 0.000 –4.716 (1.38) –7.41 to –2.03 0.001 
 Good       –3.252 (1.22) –5.65 to –0.86 0.008 –2.595 (1.21) –4.97 to –0.26 0.032 
 Very good      –2.429 (1.05) –4.49 to –0.37 0.021 –2.526 (1.06) –4.60 to –0.45 0.017 
Model 1Model 2Model 3Model 4
B (SE)95% CIPB (SE)95% CIPB (SE)95% CIPB (SE)95% CIP
GDM only –2.383 (1.03) –4.91 to –0.36 0.021 –2.434 (1.03) –4.45 to –0.41 0.018 –1.825 (1.07) –7.85 to –2.64 0.087 –2.230 (1.11) –4.41 to –0.05 0.045 
PND    –2.016 (0.75) –3.49 to –0.54 0.007    –1.816 (0.84) –3.46 to –0.17 0.031 
Pre-pregnancy SRH            
 Poor       — — — — — — 
 Fair       –5.191 (1.36) –7.85 to –2.54 0.000 –4.716 (1.38) –7.41 to –2.03 0.001 
 Good       –3.252 (1.22) –5.65 to –0.86 0.008 –2.595 (1.21) –4.97 to –0.26 0.032 
 Very good      –2.429 (1.05) –4.49 to –0.37 0.021 –2.526 (1.06) –4.60 to –0.45 0.017 

The reference groups were no diabetes, no PND, and excellent SRH.

Close to one in three women in our sample reported diabetes, a higher proportion than the general prenatal population (68). No significant associations were found between demographic characteristics, diabetes, and PND, possibly because this was a rather homogenous group. We did not find an association between diabetes and PND, which supports previous findings (69,70). A possible explanation might be that women in our study had high self-efficacy and felt they were successfully managing their disease. The majority of women with diabetes were taking diabetes-related medication (Table 1), which we hypothesize might increase confidence or self-efficacy and reduce the potential negative effects of diabetes status on their mental health because they are actively managing their condition. There is evidence to suggest that diabetes self-care and management is associated with self-efficacy and better mental health outcomes (71,72). It will be important to test our hypothesis with a larger sample of prenatal Latinas diagnosed with diabetes. However, PND was significantly associated with pregnancy SRH.

On average, participants rated their pregnancy health worse than pre-pregnancy health, suggesting that women felt worse during gestation. Others have found a similar trend, with the proportion of poor or fair SRH increasing in the third trimester (55). This shift in their perception, from good health pre-pregnancy to poorer health in pregnancy, might be an expression of pregnancy-related issues that were not assessed in this study, including poor sleep and uncomfortable weight gain, or risk factors, such as substance and/or tobacco use and economic hardship (55).

Similar to previous studies (54,55), we found that women with PND and diabetes rated their health significantly worse than individuals without these conditions. To further explore these associations, we tested the effect of PND and diabetes on pregnancy SRH and found a significant and negative association. To determine the effect of pre-pregnancy SRH, we controlled for this variable in our regression models and found that pre-pregnancy SRH reduced the effect of diabetes on pregnancy SRH, suggesting that pre-pregnancy SRH is a robust variable that may capture latent variables associated with diabetes in pregnancy. However, when PND and pre-pregnancy SRH were added to the diabetes models, we found that pre-pregnancy SRH did not reduce the effect of diabetes on pregnancy SRH, suggesting that these two variables make unique contributions that should be explored further. Others have found that as depressive symptoms increase during pregnancy, SRH worsens (56). However, these associations were not explored in the context of diabetes in prenatal women. Future studies should look at specific health conditions, maternal mood, and SRH, as well as beliefs about those conditions, to help further understand the relationships found in this study.

Although this study sheds light on the relationship between PND, diabetes, and SRH, it has some limitations. First, the study had a small, homogenous sample, making the results more specific to Latinas with similar demographic characteristics. Future studies should use larger cohorts of Latinas from diverse socioeconomic backgrounds. Additionally, subsequent studies should include non-Latinas with similar demographic characteristics to this sample to determine whether cultural beliefs or perceptions are associated with feelings about diabetes in pregnancy. Subsequent studies should explore the mediating effects of pre-pregnancy exercise, substance use, and poverty on associations between PND, diabetes, and SRH. Additionally, this study lacked pre-pregnancy metabolic data, which prevented us from exploring whether they are associated with PND and SRH. Given previous research showing a relationship between high pre-pregnancy BMI and perinatal depression (73,74), it is likely we would have had similar results. However, this speculation should be confirmed empirically. Because less is known about the association between pre-pregnancy BMI and SRH, future studies should include pre-pregnancy BMI to assess its effect on SRH. Finally, this study did not measure glucose control, which has been shown to be associated with depression during the perinatal period (75) and SRH (76) in non-perinatal populations. Therefore, future studies should include the collection of blood glucose levels from participants to test the association of glycemic status with mood and women’s own health perceptions. Finally, subsequent investigations should include a qualitative component to further understand the challenges pregnant women with diabetes face as they relate to cultural expectations and needs to allow for more culturally sensitive care and self-management.

Given findings regarding the associations between SRH, PND, and diabetes, health care providers should assess SRH throughout the course of pregnancy in women with PND to identify women who are experiencing additional effects on self-assessments because of poor mental health. Screening for poor SRH may offer providers an opportunity to educate women at risk of depression and provide coping strategies or treatment as needed.

The authors wish to thank the mothers who participated in this study. This study would not have been possible without their commitment to our work. The authors would also like to acknowledge the hard work of our impressive research assistants and technical staff. In addition, the authors thank Dr. Flavia Andrade and Dr. Dawn Aycock for feedback on early drafts of the manuscript.

This work was supported by the National Institute of Mental Health (5T32MH093315-03; Drs. Susan Girdler and David Rubinow, principal investigators), the Foundation of Hope for Research and Treatment of Mental Illness, the North Carolina Translational and Clinical Sciences Institute, the University of Illinois at Urbana-Champaign, and the Programs to Increase Diversity Among Individuals Engaged in Health-Related Research (PRIDE)-Behavioral and Sleep Medicine for mentoring support during the development of this manuscript.

No potential conflicts of interest relevant to this article were reported.

S.L.-C. conceptualized the project, secured funding, collected the data, led the data analysis, and supervised all aspects of the manuscript. C.S. contributed to the data analysis and introduction. D.M. assisted with the methods and results. H.H. contributed to the discussion. S.L.-C. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

1.
Lawrence
JM
,
Contreras
R
,
Chen
W
,
Sacks
DA
.
Trends in the prevalence of preexisting diabetes and gestational diabetes mellitus among a racially/ethnically diverse population of pregnant women, 1999–2005
.
Diabetes Care
2008
;
31
:
899
904
2.
Ferrara
A
.
Increasing prevalence of gestational diabetes mellitus: a public health perspective
.
Diabetes Care
2007
;
30
(
Suppl. 2
):
S141
S146
3.
Ferrara
A
,
Kahn
HS
,
Quesenberry
CP
,
Riley
C
,
Hedderson
MM
.
An increase in the incidence of gestational diabetes mellitus: Northern California, 1991–2000
.
Obstet Gynecol
2004
;
103
:
526
533
4.
Dabelea
D
,
Snell-Bergeon
JK
,
Hartsfield
CL
,
Bischoff
KJ
,
Hamman
RF
,
McDuffie
RS
.
Increasing prevalence of gestational diabetes mellitus (GDM) over time and by birth cohort
.
Diabetes Care
2005
;
28
:
579
584
5.
Thorpe
LE
,
Berger
D
,
Ellis
JA
, et al
.
Trends and racial/ethnic disparities in gestational diabetes among pregnant women in New York City, 1990–2001
.
Am J Public Health
2005
;
95
:
1536
1539
6.
Chen
L
,
Magliano
DJ
,
Zimmet
PZ
.
The worldwide epidemiology of type 2 diabetes mellitus: present and future perspectives
.
Nat Rev Endocrinol
2012
;
8
:
228
236
7.
Hu
FB
.
Globalization of diabetes: the role of diet, lifestyle, and genes
.
Diabetes Care
2011
;
34
:
1249
1257
8.
DeSisto
CL
,
Kim
SY
,
Sharma
AJ
.
Prevalence estimates of gestational diabetes mellitus in the United States, pregnancy risk assessment monitoring system (PRAMS), 2007–2010
.
Prev Chronic Dis
2014
;
11
:
E104
9.
Proceedings of the 4th International Workshop-Conference on Gestational Diabetes Mellitus. Chicago, Illinois, USA: 14–16 March 1997
.
Diabetes Care
1998
;
21
(
Suppl. 2
):
B1
B167
10.
Cheung
NW
,
Byth
K
.
Population health significance of gestational diabetes
.
Diabetes Care
2003
;
26
:
2005
2009
11.
Bellamy
L
,
Casas
JP
,
Hingorani
AD
,
Williams
D
.
Type 2 diabetes mellitus after gestational diabetes: a systematic review and meta-analysis
.
Lancet
2009
;
373
:
1773
1779
12.
Affonso
DD
,
Lovett
S
,
Paul
SM
,
Sheptak
S
.
A standardized interview that differentiates pregnancy and postpartum symptoms from perinatal clinical depression
.
Birth
1990
;
17
:
121
130
13.
Bennett
HA
,
Einarson
A
,
Taddio
A
,
Koren
G
,
Einarson
TR
.
Prevalence of depression during pregnancy: systematic review
.
Obstet Gynecol
2004
;
103
:
698
709
14.
McKee
M
.
Health-related functional status in pregnancy: relationship to depression and social support in a multi-ethnic population
.
Obstet Gynecol
2001
;
97
:
988
993
15.
InfoPlease
.
Hispanic Americans by the numbers
.
Available from https://www.infoplease.com/hispanic-americans-numbers. Accessed 20 May 2017
16.
Passel
JS
,
Livingston
G
,
D’Vera
C
.
Explaining why minority births now outnumber white births
.
2013
.
17.
Lara
MA
,
Le
HN
,
Letechipia
G
,
Hochhausen
L
.
Prenatal depression in Latinas in the US and Mexico
.
Matern Child Health J
2009
;
13
:
567
576
18.
King
H
,
Aubert
RE
,
Herman
WH
.
Global burden of diabetes, 1995–2025: prevalence, numerical estimates, and projections
.
Diabetes Care
1998
;
21
:
1414
1431
19.
Chasan-Taber
L
,
Fortner
RT
,
Gollenberg
A
,
Buonnaccorsi
J
,
Dole
N
,
Markenson
G
.
A prospective cohort study of modifiable risk factors for gestational diabetes among Hispanic women: design and baseline characteristics
.
J Womens Health
2010
;
19
:
117
124
20.
Bisson
M
,
Sériès
F
,
Giguère
Y
, et al
.
Gestational diabetes mellitus and sleep-disordered breathing
.
Obstet Gynecol
2014
;
123
:
634
641
21.
Kozhimannil
KB
,
Pereira
MA
,
Harlow
BL
.
Association between diabetes and perinatal depression among low-income mothers
.
JAMA
2009
;
301
:
842
847
22.
Morrison
C
,
McCook
JG
,
Bailey
BA
.
First trimester depression scores predict development of gestational diabetes mellitus in pregnant rural Appalachian women
.
J Psychosom Obstet Gynaecol
2016
;
37
:
21
25
23.
Pawluski
JL
,
Lonstein
JS
,
Fleming
AS
.
The neurobiology of postpartum anxiety and depression
.
Trends Neurosci
2017
;
40
:
106
120
24.
Goodman
JH
,
Watson
GR
,
Stubbs
B
.
Anxiety disorders in postpartum women: a systematic review and meta-analysis
.
J Affect Disord
2016
;
203
:
292
331
25.
Martini
J
,
Petzoldt
J
,
Einsle
F
,
Beesdo-Baum
K
,
Höfler
M
,
Wittchen
HU
.
Risk factors and course patterns of anxiety and depressive disorders during pregnancy and after delivery: a prospective-longitudinal study
.
J Affect Disord
2015
;
175
:
385
395
26.
Milgrom
J
,
Gemmill
AW
,
Bilszta
JL
, et al
.
Antenatal risk factors for postnatal depression: a large prospective study
.
J Affect Disord
2008
;
108
:
147
157
27.
Silverman
ME
,
Reichenberg
A
,
Savitz
DA
, et al
.
The risk factors for postpartum depression: a population-based study
.
Depress Anxiety
2017
;
34
:
178
187
28.
Dalfrà
MG
,
Nicolucci
A
,
Bisson
T
,
Bonsembiante
B
,
Lapolla
A
.
Quality of life in pregnancy and post-partum: a study in diabetic patients
.
Qual Life Res
2012
;
21
:
291
298
29.
Heron
J
,
O'Connor
TG
,
Evans
J
,
Golding
J
,
Glover
V
.
The course of anxiety and depression through pregnancy and the postpartum in a community sample
.
J Affect Disord
2004
;
80
:
65
73
30.
Rubertsson
C
,
Waldenström
U
,
Wickberg
B
,
Rådestad
I
,
Hildingsson
I
.
Depressive mood in early pregnancy and postpartum: Prevalence and women at risk in a national Swedish sample
.
J Reprod Infant Psychol
2005
;
23
:
155
166
31.
Marcus
SM
,
Flynn
HA
,
Blow
FC
,
Barry
KL
.
Depressive symptoms among pregnant women screened in obstetrics settings
.
J Womens Health
2003
;
12
:
373
380
32.
Larsson
C
,
Sydsjö
G
,
Josefsson
A
.
Health, sociodemographic data, and pregnancy outcome in women with antepartum depressive symptoms
.
Obstet Gynecol
2004
;
104
:
459
466
33.
Kurki
T
,
Hiilesmaa
V
,
Raitasalo
R
,
Mattila
H
,
Ylikorkala
O
.
Depression and anxiety in early pregnancy and risk for preeclampsia
.
Obstet Gynecol
2000
;
95
:
487
490
34.
Dayan
J
,
Creveuil
C
,
Marks
MN
, et al
.
Prenatal depression, prenatal anxiety, and spontaneous preterm birth: a prospective cohort study among women with early and regular care
.
Psychosom Med
2006
;
68
:
938
946
35.
Steer
RA
,
Scholl
TO
,
Hediger
ML
,
Fischer
RL
.
Self-reported depression and negative pregnancy outcomes
.
J Clin Epidemiol
1992
;
45
:
1093
1099
36.
Davis
EP
,
Glynn
LM
,
Schetter
CD
,
Hobel
C
,
Chicz-Demet
A
,
Sandman
CA
.
Prenatal exposure to maternal depression and cortisol influences infant temperament
.
J Am Acad Child Adolesc Psychiatry
2007
;
46
:
737
746
37.
Davis
EP
,
Snidman
N
,
Wadhwa
PD
,
Glynn
LM
,
Schetter
CD
,
Sandman
CA
.
Prenatal maternal anxiety and depression predict negative behavioral reactivity in infancy
.
Infancy
2004
;
6
:
319
331
38.
Diego
MA
,
Field
T
,
Hernandez-Reif
M
.
Prepartum, postpartum and chronic depression effects on neonatal behavior
.
Infant Behav Dev
2005
;
28
:
155
164
39.
Huot
RL
,
Brennan
PA
,
Stowe
ZN
,
Plotsky
PM
,
Walker
EF
.
Negative affect in offspring of depressed mothers is predicted by infant cortisol levels at 6 months and maternal depression during pregnancy, but not postpartum
.
Ann N Y Acad Sci
2004
;
1032
:
234
236
40.
Howard
LM
,
Kirkwood
G
,
Latinovic
R
.
Sudden infant death syndrome and maternal depression
.
J Clin Psychiatry
2007
;
68
:
1279
1283
41.
Deave
T
,
Heron
J
,
Evans
J
,
Emond
A
.
The impact of maternal depression in pregnancy on early child development
.
BJOG
2008
;
115
:
1043
1051
42.
American Diabetes Association
.
Gestational diabetes mellitus
.
Diabetes Care
2003
;
26
(
Suppl. 1
):
S103
43.
Wier
L
,
Witt
E
,
Burgess
J
,
Elixhauser
A
.
Hospitalizations related to diabetes in pregnancy, 2008. HCUP statistical brief #102
.
Rockville
,
Md., Agency for Healthcare Research and Quality
,
2010
44.
Bryant
AS
,
Worjoloh
A
,
Caughey
AB
,
Washington
AE
.
Racial/ethnic disparities in obstetric outcomes and care: prevalence and determinants
.
Am J Obstet Gynecol
2010
;
202
:
335
343
45.
Wolf
M
,
Shah
A
,
Jimenez-Kimble
R
,
Sauk
J
,
Ecker
JL
,
Thadhani
R
.
Differential risk of hypertensive disorders of pregnancy among Hispanic women
.
J Am Soc Nephrol
2004
;
15
:
1330
1338
46.
Evers
I
,
De Valk
H
,
Mol
B
,
Ter Braak
EW
,
Visser
G
.
Macrosomia despite good glycaemic control in type I diabetic pregnancy; results of a nationwide study in The Netherlands
.
Diabetologia
2002
;
45
:
1484
1489
47.
Persson
M
,
Pasupathy
D
,
Hanson
U
,
Norman
M
.
Birth size distribution in 3,705 infants born to mothers with type 1 diabetes: a population-based study
.
Diabetes Care
2011
;
34
:
1145
1149
48.
Yang
J
,
Cummings
EA
,
O’Connell
C
,
Jangaard
K
.
Fetal and neonatal outcomes of diabetic pregnancies
.
Obstet Gynecol
2006
;
108
:
644
650
49.
Wojcicki
J
,
Hessol
NA
,
Heyman
MB
,
Fuentes-Afflick
E
.
Risk factors for macrosomia in infants born to Latina women
.
J Perinatol
2008
;
28
:
743
50.
Ogden
CL
,
Carroll
MD
,
Flegal
KM
.
High body mass index for age among US children and adolescents, 2003–2006
.
JAMA
2008
;
299
:
2401
2405
51.
Wu
S
,
Wang
R
,
Zhao
Y
, et al
.
The relationship between self-rated health and objective health status: a population-based study
.
BMC Public Health
2013
;
13
:
320
52.
Undén
AL
,
Elofsson
S
,
Andréasson
A
,
Hillered
E
,
Eriksson
I
,
Brismar
K
.
Gender differences in self-rated health, quality of life, quality of care, and metabolic control in patients with diabetes
.
Gender Med
2008
;
5
:
162
180
53.
Idler
EL
,
Benyamini
Y
.
Self-rated health and mortality: a review of twenty-seven community studies
.
J Health Soc Behav
1997
;
38
:
21
37
54.
Schytt
E
,
Waldenström
U
.
Risk factors for poor self-rated health in women at 2 months and 1 year after childbirth
.
J Womens Health
2007
;
16
:
390
405
55.
Haas
JS
,
Jackson
RA
,
Fuentes-Afflick
E
, et al
.
Changes in the health status of women during and after pregnancy
.
J Gen Intern Med
2005
;
20
:
45
51
56.
Orr
ST
,
Blazer
DG
,
James
SA
,
Reiter
JP
.
Depressive symptoms and indicators of maternal health status during pregnancy
.
J Womens Health
2007
;
16
:
535
542
57.
Rumbold
AR
,
Crowther
VA
.
Women’s experiences of being screened for gestational diabetes mellitus
.
Aust N Z J Obstet Gynaecol
2002
;
42
:
131
137
58.
Cavazos-Rehg
PA
,
Zayas
LH
,
Spitznagel
EL
.
Legal status, emotional well-being and subjective health status of Latino immigrants
.
J Natl Med Assoc
2007
;
99
:
1126
59.
Pérez-Escamilla
R
,
Putnik
P
.
The role of acculturation in nutrition, lifestyle, and incidence of type 2 diabetes among Latinos
.
J Nutr
2007
;
137
:
860
870
60.
Chasan-Taber
L
,
Braun
B
,
Whitcomb
BW
.
Review of self-reported physical activity assessments for pregnancy: summary of the evidence for validity and reliability
.
Obstet Gynecol
2015
;
126
:
676
677
61.
Pineda Olvera
AE
,
Stewart
SM
,
Galindo
L
,
Stephens
J
.
Diabetes, depression, and metabolic control in Latinas
.
Cultur Divers Ethnic Minor Psychol
2007
;
13
:
225
62.
Lara-Cinisomo
S
,
Plott
J
,
Grewen
K
,
Meltzer-Brody
S
.
The feasibility of recruiting and retaining perinatal Latinas in a biomedical study exploring neuroendocrine function and postpartum depression
.
J Immigr Minor Health
2016
;
5
:
1
9
63.
Murray
D
,
Cox
JL
.
Screening for depression during pregnancy with the Edinburgh Depression Scale (EDDS)
.
J Reprod Infant Psychol
1990
;
8
:
99
107
64.
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
786
65.
Yonkers
KA
,
Ramin
SM
,
Rush
AJ
, et al
.
Onset and persistence of postpartum depression in an inner-city maternal health clinic system
.
Am J Psychiatry
2001
;
158
:
1856
1863
66.
Jadresic
E
,
Araya
R
,
Jara
C
.
Validation of the Edinburgh postnatal depression scale (EPDS) in Chilean postpartum women
.
J Psychosom Obstet Gynaecol
1995
;
16
:
187
191
67.
Kraus
MW
,
Adler
N
,
Chen
TWD
.
Is the association of subjective SES and self-rated health confounded by negative mood? An experimental approach
.
Health Psychol
32
:
138
145
68.
King
H
,
Rewers
M
.
Global estimates for prevalence of diabetes mellitus and impaired glucose tolerance in adults
.
Diabetes Care
1993
;
16
:
157
177
69.
Engberg
E
,
Stach-Lempinen
B
,
Sahrakorpi
N
, et al
.
A cross-sectional study of antenatal depressive symptoms in women at high risk for gestational diabetes mellitus
.
J Psychosom Res
2015
;
79
:
646
650
70.
Katon
JG
,
Russo
J
,
Gavin
AR
,
Melville
JL
,
Katon
WJ
.
Diabetes and depression in pregnancy: is there an association?
J Womens Health
2011
;
20
:
983
989
71.
Williams
K
,
Bond
M
.
The roles of self-efficacy, outcome expectancies and social support in the self-care behaviours of diabetics
.
Psychol Health Med
2002
;
7
:
127
141
72.
Ciechanowski
PS
,
Katon
WJ
,
Russo
JE
,
Hirsch
IB
.
The relationship of depressive symptoms to symptom reporting, self-care and glucose control in diabetes
.
Gen Hosp Psychiatry
2003
;
25
:
246
252
73.
Bodnar
LM
,
Wisner
KL
,
Moses-Kolko
E
,
Sit
DK
,
Hanusa
BH
.
Prepregnancy body mass index, gestational weight gain and the likelihood of major depression during pregnancy
.
J Clin Psychiatry
2009
;
70
:
1290
74.
LaCoursiere
D
,
Barrett-Connor
E
,
O’Hara
MW
,
Hutton
A
,
Varner
MW
.
The association between prepregnancy obesity and screening positive for postpartum depression
.
BJOG
2010
;
117
:
1011
1018
75.
Lustman
PJ
,
Anderson
RJ
,
Freedland
KE
,
De Groot
M
,
Carney
RM
,
Clouse
RE
.
Depression and poor glycemic control: a meta-analytic review of the literature
.
Diabetes Care
2000
;
23
:
934
942
76.
Nielsen
AB
,
Gannik
D
,
Siersma
V
,
de Fine Olivarius
VN
.
The relationship between HbA1c level, symptoms and self-rated health in type 2 diabetic patients
.
Scand J Prim Health Care
2011
;
29
:
157
164
Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0 for details.