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Published in final edited form as: J Perinatol. 2021 Aug 16;42(6):708–713. doi: 10.1038/s41372-021-01186-4

Maternal perceived stress and the increased risk of preterm birth in a majority non-Hispanic Black pregnancy cohort

Sara L Kornfield 1,*, Valerie M Riis 2, Clare McCarthy 2, Michal A Elovitz 2, Heather H Burris 2,3,4
PMCID: PMC8847548  NIHMSID: NIHMS1736918  PMID: 34400775

Abstract

Objective:

To determine whether perceived stress is associated with preterm birth (PTB) and to investigate racial differences in stress and PTB.

Study Design:

A secondary analysis of a prospective cohort study of 1,911 women with singleton pregnancies examined responses to psychosocial stress questionnaires at 16-20 weeks of gestation.

Results:

High perceived stress (19%) and PTB (10.8%) were prevalent in our sample (62% non-Hispanic Black). Women with PTB were more likely to be Black, have chronic hypertension (cHTN), pre-gestational diabetes, and higher BMI. Women with high perceived stress had more PTBs than those with lower stress (15.2% vs. 9.8%), and stress was associated with higher odds of PTB (aOR: 1.55, 95% CI: 1.09-2.19).

Conclusion:

The significant association between high perceived stress and PTB suggests that prenatal interventions to reduce maternal stress could improve the mental health of pregnant women and may result in reduced rates of PTB.

INTRODUCTION

Preterm birth (PTB), a birth that occurs prior to 37 completed weeks of gestation, is a major public health issue in the United States that affects approximately 10% of births and is responsible for one-third of infant deaths,1 50% of long-term neurological sequelae,1 and $26.2 billion in costs annually.2 Epidemiologic risk factors for PTB include maternal smoking, medical comorbid conditions, and self-reported non-Hispanic Black race/ethnicity. Given that race is a social, not a biological or genetic construct, 3 it is critical to understand the individual and societal factors such as stress that may lead to increased risk of PTB among Black pregnant women in the United States.

Psychosocial stress refers to the cognitive appraisal of the discrepancy between a demand and an individual’s ability to meet it. In US4-6 and international samples, 7 maternal prenatal stress has been found to be associated with PTB as well as other poor birth outcomes including low birth weight, and intrauterine growth restriction. While it has been well-established that Black women have an increased risk to PTB compared to White women, studies have not routinely focused on the contribution of maternal prenatal stress to the racial differences in birth outcome. Stress can lead to physiologic changes such as increases in cortocotrophin releasing hormone (CRH), prostaglandins, and inflammatory cytokines that may result in uterine contractions and/or spontaneous PTB. 8-10 Despite plausible biological pathways implicating stress in PTB, studies examining its impact have been equivocal11-14 likely due to the incomplete understanding of the association between perceived psychosocial stress and birth outcomes.15

While the underlying pathophysiology of PTB remains incompletely understood, PTB can be dichotomized as either medically-indicated (mPTB) secondary to conditions in either the pregnant woman or the fetus, or as spontaneous (sPTB) occurring after spontaneous rupture of membranes or preterm labor. sPTB accounts for over two-thirds of all PTBs. 1,16 While there are some data suggesting inflammatory processes,17 maternal psychological factors,18 diet and/or the microbiome19 play a role in sPTB, the precise pathogenesis of sPTB and how these factors contribute to sPTB are not elucidated and directed therapeutics are lacking. Similarly, neuroendocrine and inflammatory processes, such as those associated with stress and maternal lifestyle and behavioral processes, may contribute to the medical etiology of some mPTBs including gestational hypertension and diabetes.20-23

The neuroendocrine milieu of pregnancy is unique, with dramatic alterations in HPA axis regulation and neurosteroid production. Pregnancy represents a state of heightened cortisol and corticotrophin releasing hormone (CRH) production where cortisol stimulates the release of placental CRH and both play a role in fetal maturation and the “parturition clock.” It has been suggested that maternal psychosocial distress is related to disruptions in typical cortisol trajectories during gestation, 24 and numerous studies have indicated that placental CRH production remains sensitive to maternal psychological stress, 25 both of which are likely to increase the risk of PTB. 26 27 28

The PTB rate in the United States has worsened for a fourth year, from 9.6% in 2015 to 10.0% in 2018 when data was last available.29 This upward trend is largely due to increases in PTB among non-Hispanic Black women.30 Compared to non-Hispanic White women, Black women’s risk of PTB was 1.5 times higher (14.13% vs. 9.09%).1, 30 The reason for this persistent disparity in pregnancy outcome is not known, but hypothesized to be related to the well-known racial disparities in social determinants of health including systemic racism. It has been well documented that Black women report higher rates of perceived stress, depression, and other mental illness during pregnancy compared to White women, regardless of income.31-40 These racial disparities are not explained by lack of health care access, socioeconomic status, or genetics.35, 37, 41, 42

While psychosocial stress, depression, and other general distress are common during pregnancy,33, 37 the extent to which stress is associated with PTB, especially in largely Black pregnancy cohorts is not well studied. Thus, the objectives of this study were to quantify associations of perceived stress in pregnancy with PTB and its subtypes (sPTB and mPTB) in a large prospective, majority Black pregnancy cohort wherein we hypothesized that higher self-reported stress scores would be associated with PTB. We also sought to explore racial differences in stress and PTB between non-Hispanic Black and White women; we hypothesized that we would find higher reports of stress among Black women, and that this would be associated with PTB.

MATERIALS AND METHODS

Study Setting

This study was a planned secondary analysis of a cohort of 2,000 women enrolled from December 2013 through February 2017.43 Eligibility for the parent study was restricted to pregnant women with a gestational age of 160-206 weeks at the time of the first study visit. Exclusion criteria included: 1) major fetal anomaly, 2) HIV+, 3) history of organ transplant, 4) chronic steroid use 5) enrollment into the study during a previous pregnancy, or 6) multiple gestations (mechanisms leading to PTB in twins is different from singletons). Patients were enrolled at 3 prenatal care clinics at the Hospital of the University of Pennsylvania. Two follow-up visits occurred between 200-246 and 240-286 weeks GA. Enrollment and follow-up visits occurred at regularly scheduled prenatal visits approximately every 4 weeks until the 3 study visits were completed. This study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board at the University of Pennsylvania; all participants gave consent (IRB #818914).

Covariate and exposure (perceived stress) data

Maternal demographics, obstetric history, and pregnancy outcomes were abstracted from the Electronic Medical Record. Perceived stress was measured using the Cohen’s Perceived Stress Scale (PSS-14), a 14-item survey.44 Although the PSS-14 is not specific to pregnancy, it has been validated and widely used during pregnancy. 44-47 According to previously validated measurement data, women were considered to have high perceived stress if they scored above a cutoff score of 30 on the PSS-14.48 Participants completed surveys at each of the 3 study visits, but we used the responses from the initial study visit (16-20 weeks of gestation) because it had the most complete data and previously published data supports the role of earlier prenatal stress in contributing to the risk of PTB.49

Cohort and imputations

A total of 2,982 pregnant women were approached for the study. Among those approached, 982 (33%) declined, 57 were lost to follow-up, 23 were missing birth outcomes and 9 had no PSS-14 data from any visit (Figure 1). The final analytic cohort included 1,911 women with original or derived PSS-14 scores and birth outcome information. Of these 1,911 women, 103 were missing PSS-14 scores at the initial study visit (16-20 weeks of gestation). We imputed the initial visit PSS-14 score in one of two ways. For the 89 women with incomplete scales, but missing fewer than 3 questions, we averaged the responses from the remaining questions to determine the final score (scaling). If a woman were missing an entire questionnaire but completed it at a following visit, we used the score from that questionnaire (n=14).

Figure 1.

Figure 1.

Study enrollment flow chart

Outcome- preterm birth (PTB)

PTB was defined as delivery at <37 weeks. Secondary outcomes of sPTB and mPTB were adjudicated by a maternal-medicine physician (ME) to confirm the presence of preterm rupture of membranes or preterm labor to designate a PTB as sPTB and to identify the indication for mPTB.43

Data Analysis

Bivariate analysis was performed using Pearson chi-square tests for categorical variables, and two-sided t-tests for continuous variables. Covariates were considered for inclusion in the final model if they were hypothesized a priori to be clinically relevant, and were retained if they substantially (>10%) modified the association of interest. We utilized multivariable logistic regression models to examine the association between high perceived stress at 16-20 weeks of gestation (PSS-14 ≥30) and PTB. In secondary analyses, we examined the association between high perceived stress and specific type of PTB in separate models (sPTB and mPTB). To assess whether a “dose-response” effect may exist and to further justify our findings, we examined the association between quartiles of PSS-14 scores and PTB, where Q1 represents the lowest scores and Q4 the highest. Additionally, we assessed the association between quartiles of PSS-14 score and PTB after stratifying by race. As a sensitivity analysis, we assessed the association in the original (non-imputed) cohort, which included only women with complete PSS-14 scores at the initial visit. Odds ratios (ORs) and 95% confidence intervals (CIs) for PTB associated with high PSS-14 at this study visit were obtained. Due to differences in stress in this cohort by race and differences in PTB rates by race, 34 we added stress to a model of race and PTB to examine whether stress might mediate racial disparities in preterm birth in this cohort. We also performed race stratified models and tested for interaction between race and stress on the outcome of PTB. Statistical analyses were conducted using STATA® 14 software.

RESULTS

Demographics

Demographics, overall and by PTB status, are presented in Table 1. A total of 206 (10.8%) of the 1,911 women experienced a PTB. Maternal characteristics were compared between PTB and term births. Non-Hispanic Black women represented 62.0% of the sample, and the average age was 28.5 years, pregnant individuals with a PTB were more likely to be non-Hispanic Black, have an overweight or obese BMI, chronic hypertension (cHTN), and pre-gestational diabetes (Table 1).

Table 1.

Characteristics of 1,911 participants in Motherhood & Microbiome cohort with perceived stress data by preterm birth

Maternal characteristics All
(n=1911)
Term birth
(n=1705)
Preterm birth
(n=206)
P-value
Age 0.700
 <20 123 (6.4) 111 (6.5) 12 (5.8)
 20-34 1448 (75.8) 1287 (75.5) 161 (78.2)
 >34 340 (17.8) 307 (18.0) 33 (16.0)
BMIc 0.008
 <25 648 (33.9) 596 (35.0) 52 (25.2)
 25-29 524 (27.4) 468 (27.4) 56 (27.2)
 ≥30 719 (38.0) 624 (37.0) 95 (46.8)
Race/Ethnicity
 Non-Hispanic Black 1184 (62.0) 1036 (60.8) 148 (71.8) 0.005b
 Non-Hispanic White 521 (27.3) 480 (28.2) 41 (19.9)
 Hispanic/Latina 79 (4.1) 69 (4.1) 10 (4.9)
 Non-Hispanic Asian/Other 127 (6.7) 120 (7.0) 7 (3.4)
Gestational Age at Delivery in
weeks (Mean,SD)d
38.2 (3.0)
39.0 (1.2) 31.9 (5.1) <0.001a
Obstetric history <0.001
 Nulliparous 840 (44.0) 759 (44.5) 81 (39.3)
 Multiparous with term births 860 (45.0) 791 (46.4) 69 (33.5)
 Prior PTB 211 (11.0) 155 (9.1) 56 (27.2)
Psychiatric historye 309 (16.2) 268 (15.7) 41 (19.9) 0.123
CES-D ≥16 V1f,g 561 (31.8) 488 (30.9) 73 (38.8) 0.028
PDQ ≥17 V1f,h 390 (22.5) 344 (22.3) 46 (24.1) 0.570
Medicaid insurance 990 (51.8) 875 (51.3) 115 (55.8) 0.222
Single marital status 1254 (65.6) 1116 (65.5) 138 (67.0) 0.661
Chronic hypertension 111 (5.8) 83 (4.9) 28 (13.6) <0.001
Tobacco use in pregnancyi 171 (9.0) 146 (8.6) 25 (12.2) 0.087
Pre-gestational diabetes 44 (2.3) 33 (1.9) 11 (5.3) 0.002
PSS-14 ≥ 30 363 (19.0) 308 (18.1) 55 (26.7) 0.003
PSS-14 (Mean, SD) 22.5 (7.8) 22.3 (8.0) 24.2 (7.8) 0.001a

Abbreviations: PTB, Preterm Birth (birth <37 weeks gestational age); PSS, Cohen’s Perceived Stress Scale (14 items); V1, Visit 1; V2, Visit 2; V3, Visit 3; CES-D, The Center for Epidemiologic Studies Depression Scale; PDQ, Prenatal Distress Questionnaire

Data presented as n (col %), Chi-square p-value unless otherwise indicated.

a

Two-sided t-test

b

Fisher’s exact test

c

n=20 missing BMI

d

n=26 missing gestational age at delivery

e

Reported psychiatric health history in Electronic Medical Record problem list

f

Defined as screened positive at individual visit

g

n=145 missing CES-D score at V1

h

n=175 missing PDQ at V1

i

n=4 missing tobacco use

PSS-14

Mean PSS-14 score was 22.3 (SD 8.0) for term births and 24.2 (SD 7.8) for PTBs (p=0.001). Among women with high perceived stress (PSS-14 ≥30), the preterm birth rate was 15.2% compared to 9.7% among women with lower stress scores (p=0.003) (Table 1). In the unadjusted logistic regression model, there was a positive, significant association between PSS-14 ≥30 and PTB (OR:1.65, 95% CI: 1.18-2.30). The association remained significant after adjusting for race, BMI, Medicaid insurance, obstetric history, pre-gestational diabetes, and cHTN (aOR: 1.47, 95% CI: 1.03-2.08) (Table 2). Additionally, we found an increasing adjusted odds ratio for each quartile compared to Q1, with participants in Q4 having the highest odds of PTB (aOR: 1.50, 95% CI: 0.98-2.28) (Table 3). Results were similar in complete case analysis (Supplemental Table 1).

Table 2:

Association between high perceived stress (PSS-14 ≥30) and preterm birth (n=1,911)

Perceived stress levels Model 1 Model 2a Model 3a Model 4a
PSS-14 ≥30 1.65 (1.18-2.30) 1.56 (1.10-2.21) 1.50 (1.06-2.12) 1.47 (1.03-2.08)
PSS-14 <30 Ref Ref Ref Ref
Model 1: Crude association between high PSS and PTB
Model 2: Adjusted for Medicaid insurance, obstetric history, and BMI
Model 3: Model 2 + race/ethnicity
Model 4: Model 3 + pre-gestational diabetes, and chronic hypertension
a

n=20 missing BMI

Table 3.

Association between quartiles of Perceived Stress Scale (PSS-14) and preterm birth (n=1,911)

Quartiles of PSS-14 Preterm birth n (%)* Crude OR (95% CI) aOR^ (95% CI)
Q1 (2-17) (n=546) 48 (8.7) Ref Ref
Q2 (18-22) (n=430) 39 (9.1) 1.03 (0.66-1.61) 0.99 (0.63-1.56)
Q3 (23-28) (n=485) 55 (11.3) 1.33 (0.88-2.00) 1.24 (0.81-1.90)
Q4 (29-55) (n=450) 64 (14.2) 1.72 (1.16-2.56) 1.50 (0.98-2.28)
*

Chi Square test, p=0.026

^

Adjusted for Medicaid insurance, obstetric history, BMI, race/ethnicity, pre-gestational diabetes, and chronic hypertension

Phenotypes of PTB

The different pathogeneses of PTB phenotypes led us to build separate models examining the association between high PSS-14 score and sPTB and high PSS-14 score and mPTB. We found significant positive associations between both high stress and sPTB (OR: 1.55, 95% CI: 1.01-2.37) and high stress and mPTB (OR: 1.81, 95% CI: 1.11-2.96) in crude models. In both models, the associations became non-significant after adjustment for race, BMI, Medicaid insurance, obstetric history, pre-gestational diabetes, and cHTN (Supplemental Table 2).

Race/ethnicity, perceived stress, and PTB

A higher proportion of non-Hispanic Black women (24.7 %) had a PSS-14 score ≥ 30 than White women (7.7%) (p<0.001). Black women also had higher rates of PTB (12.5%) compared to White women (7.9%) (p=0.007). However we did not detect PSS-14 score to be a significant mediator of the race-PTB association. The Black-White disparity in PTB in adjusted models without PSS-14 was OR = 1.76, 95% CI: 1.13-2.76). When PSS14 ≥ 30 was added to model, the effect estimate was unchanged (aOR =1.64, 95% CI: 1.05-2.58) (Table 4). However, there were only four White women with both high PSS-14 and PTB.

Table 4.

Association of race and preterm birth, unadjusted, covariate- adjusted, and additionally adjusted for high perceived stress (n= 1,705)

Race Model 1 Model 2 Model 3
Non-Hispanic Black 1.67 (1.16-2.40) 1.76 (1.13-2.76) 1.64 (1.05-2.58)
Non-Hispanic White Ref Ref Ref
Model 1: Crude association between non-hispanic black race and PTB
Model 2: Adjusted for Medicaid insurance, BMI, obstetric history, pre-gestational diabetes, and chronic hypertension (cHTN)
Model 3: Model 2 + high PSS≥30 at V1

In models restricted to non-Hispanic Black women, those with PSS-14 ≥ 30 had significantly higher odds of PTB compared to those with lower perceived stress scores (OR = 1.50, 95% CI: 1.03-2.19) and this association remained significant when adjusted for Medicaid insurance, obstetric history, BMI, pre-gestational diabetes, and cHTN (aOR = 1.59, 95% CI: 1.08-2.34). Among Non-Hispanic White women, high stress was not significantly associated with increased odds of PTB (aOR 1.10, 95% CI: 0.34-3.55). However, the interaction between race and high stress was not significant (p=0.84). For maternal characteristics by race, see Supplemental Table 3.

DISCUSSION

In a large, majority non-Hispanic Black cohort of pregnant women, we found that high perceived stress during pregnancy is associated with PTB. Overall, the prevalence of above threshold scores on the PSS-14 were substantially higher among Black women compared to non-Black women in our cohort, and Black women were more likely to experience a PTB. Among non-Hispanic Black women, those with higher reported stress were 1.5 times more likely to have a PTB. This finding suggests that stress may have an additive effect in already vulnerable populations which may influence biological processes such as parturition and is consistent with the “weathering” hypothesis which suggests that chronic exposure to social and economic disadvantage leads to accelerated decline in physical health outcomes and could partially explain racial disparities in a wide array of health conditions, 50-52 including PTB. 53

The precise biological mechanisms linking perceived stress and PTB remain unclear. Investigations into the associations between biomarkers of stress, self-reported stress and support, and sPTB have been equivocal.11-15 While some work has found no association between PTB and biomarkers including maternal serum cortisol, corticotrophin-releasing hormone (CRH), and adrenocorticotrophic hormone (ACTH) and reports of maternal psychosocial stress and perceived support, 19 others have found that stress/distress may affect inflammatory cytokines, which were associated with PTB.54 Further research exploring a more comprehensive assessment of maternal immune responses to stress and depression throughout pregnancy may yield additional insight into these associations. While differences in psychosocial stress alone are insufficient to explain racial disparities in PTB,40 understanding the mechanisms linking psychosocial distress before and during pregnancy to PTB among Black women may be critical to improving birth outcomes among Black women.

As high rates of stress and depression (which may contribute to perceived stress) have been reported in both pregnant and non-pregnant Black women, our findings of elevated levels of stress in pregnant non-Hispanic Black women may not be specific to pregnancy. 50, 54-56 However it is likely that pre-pregnancy stress is associated with prenatal stress. This study cannot determine if pregnancy modifies or exacerbates that level of stress.

This study has some limitations. The 3 time points spanned only a 12-week time period within the second trimester of pregnancy. Psychological conditions might change over a greater period of time than 12 weeks, and stress may increase as pregnancy progresses. Our data cannot determine whether PTB is associated with transient depression and psychological distress that resolved prior to the first visit assessment or increased after it. Further, this cohort included women who presented for a prenatal visit prior to 206 weeks. Patients who present >206/7 weeks of pregnancy might be at a higher risk for both stress and PTB. This study did not account for other psychosocial (i.e., experience of discrimination or racism; or trauma) or genetic factors that contribute to stress and/or the outcome of PTB. While we gathered medical record data on psychiatric history, this was based on problem list designation which does not differentiate between current and past disorders. These data relies on individual providers adding the diagnosis to the medical record problem list which may result in an underestimate of psychiatric disorders in this sample. Similarly, we did not assess for participant substance use disorders, other than tobacco use in pregnancy. Imputed data carries its own limitations, however our results were similar in the non-imputed, complete-case analysis. Although sPTB and mPTB were combined in the primary model, secondary analyses show that high stress may act similarly on PTB regardless of phenotype. Lastly, while we hypothesized a mediating effect of perceived stress on the relationship between race and PTB this study was ultimately underpowered to detect this effect as only four White women with high PSS-14 score had a PTB. Similarly, the study was underpowered to detect an interaction between race and stress.

Strengths of the study include that it is a large, prospective cohort, with well-phenotyped cases of PTB and a high proportion of Black women, who are historically understudied but at higher risk for PTB. Further, this study used a well-validated measure to assess psychosocial wellbeing. Finally, our study confirmed that the PSS-14 is an easily administered tool that can be used during pregnancy to quickly identify women at highest risk for heightened distress that may warrant the further attention of a mental health provider.

CONCLUSIONS

In this study, we demonstrate associations between maternal perceived stress and PTB. Specifically, perceived stress was significantly associated with PTB for all women. Although this study was not powered to detect the role of stress as a mediator between race and PTB, we did confirm previous findings suggesting that Black women report more perceived stress than non-Hispanic White women.57 These results suggest that there is utility in screening and referral to evidence-based mental health intervention for stress that could potentially modify the PTB rate, which is particularly important for Black women who have excess PTB risk.58 The American College of Obstetricians and Gynecologists (ACOG) recommends screening for prenatal depression and psychosocial stress at least once during pregnancy using a standardized, validated tool to help prevent severe post-partum depression, impaired mother-infant interactions, suicide, and infanticide.59 In the last decade, an increased interest in prevention and treatment of postpartum depression has motivated perinatal screening and referral to treatment, however perceived stress and depression are distinct constructs. 57 Measuring depression alone may overlook a woman’s level of perceived stress, which may be associated with poor pregnancy outcomes, including PTB. While stress is related to, and contributes to, depression and anxiety, the current findings suggest that even non-pathological experiences of stress are associated with significant health risks to both mother and child. Given that perceived stress may be a modifiable variable, future research should investigate stress management interventions for pregnant women.

Supplementary Material

Supplemental Tables

Footnotes

Disclosure: The authors have no conflicts of interest to disclose.

REFERENCES

  • 1.Matthews TJ, MacDorman MF, Thoma ME. Infant mortality statistics from the 2013 period linked birth/infant death data set. National Center for Health Statistics. Vital Health Stat. 2015;64:1–30. [PubMed] [Google Scholar]
  • 2.Committee on understanding premature birth and assuring healthy outcomes. Preterm Birth: Causes, Consequences, and Prevention. National Academies Press; 2007. [PubMed] [Google Scholar]
  • 3.“On racism: A new standard for publishing on racial health inequities,” Health Affairs Blog, July 2, 2020. DOI: 10.1377/hblog20200630.939347 [DOI] [Google Scholar]
  • 4.Rini CK, Dunkel-Schetter C, Wadhwa PD, Sandman CA. Psychological adaptation and birth outcomes: the role of personal resources, stress, and sociocultural context in pregnancy. Health Psychol 1999; 18: 333–45. [DOI] [PubMed] [Google Scholar]
  • 5.Copper RL, Goldenberg RL, Das A, Elder N, Swain M, Norman G, et al. The preterm prediction study: maternal stress is associated with spontaneous preterm birth at less than thirty-five weeks' gestation. National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network. Am J Obstet Gynecol. 1996. Nov;175(5):1286–92. doi: 10.1016/s0002-9378(96)70042-x. PMID: 8942502. [DOI] [PubMed] [Google Scholar]
  • 6.Dole N, Savitz DA, Hertz-Picciotto I, Siega-Riz AM, McMahon MJ, Buekens P. Maternal stress and preterm birth. Am J Epidemiol. 2003. Jan 1;157(1):14–24. doi: 10.1093/aje/kwf176. PMID: 12505886. [DOI] [PubMed] [Google Scholar]
  • 7.Rondó PH, Ferreira RF, Nogueira F, Ribeiro MC, Lobert H, Artes R. Maternal psychological stress and distress as predictors of low birth weight, prematurity and intrauterine growth retardation. Eur J Clin Nutr. 2003. Feb;57(2):266–72. doi: 10.1038/sj.ejcn.1601526. PMID: 12571658. [DOI] [PubMed] [Google Scholar]
  • 8.Guendelman S, Kosa JL, Pearl M, Graham S & Kharrazi M. Exploring the relationship of second-trimester corticotropin releasing hormone, chronic stress and preterm delivery. The Journal of Maternal-Fetal & Neonatal Medicine. 2008. 21(11), 788–795. 10.1080/14767050802379031. [DOI] [PubMed] [Google Scholar]
  • 9.Levine TA, Alderdice FA, Grunau RE, & McAuliffe FM. Prenatal stress and hemodynamics in pregnancy: A systematic review. Archives of Women’s Mental Health. 2016. 19(5), 721–739. 10.1007/s00737-016-0645-1. [DOI] [PubMed] [Google Scholar]
  • 10.Ruiz RJ, Gennaro S, O’Connor C, Dwivedi A, Gibeau A, Keshinover T, et al. CRH as a predictor of preterm birth in minority women. Biological Research for Nursing. 2016. 18(3), 316–321. 10.1177/1099800415611248. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Arbour MW, Corwin EJ, Salsberry PJ, & Atkins M Racial differences in the health of childbearing-aged women. MCN: The American Journal of Maternal/Child Nursing. 2012. 37(4), 262–268. 10.1097/NMC.0b013e31824b544e. [DOI] [PubMed] [Google Scholar]
  • 12.Khashan AS, McNamee R, Abel KM, Mortensen PB, Kenny LC, Pedersen MG et al. Rates of preterm birth following antenatal maternal exposure to severe life events: A population-based cohort study. Human Reproduction. 2009; 24(2), 429–437. 10.1093/humrep/den418. [DOI] [PubMed] [Google Scholar]
  • 13.Kramer MR, Hogue CJ, Dunlop AL, & Menon R. Preconceptional stress and racial disparities in preterm birth: An overview. Acta Obstetricia et Gynecologica Scandinavica. 2011. 90(12), 1307–1316. 10.1111/j.1600-0412.2011.01136.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Kramer MS, Lydon J, Seguin L, Goulet L, Kahn SR, McNamara H, et al. Stress pathways to spontaneous preterm birth: The role of stressors, psychological distress, and stress hormones. American Journal of Epidemiology. 2009. 169(11), 1319–1326. 10.1093/aje/kwp061. [DOI] [PubMed] [Google Scholar]
  • 15.Wheeler S, Maxson P, Truong T, Swamy G. Psychosocial Stress and Preterm Birth: The Impact of Parity and Race. Matern Child Health J. 2018. 22, 1430–1435. 10.1007/s10995-018-2523-0 [DOI] [PubMed] [Google Scholar]
  • 16.Gyamfi-Bannerman C, Ananth C. Trends in spontaneous and indicated preterm delivery among singleton gestations in the United States, 2005-2012. Obstet Gynecol. 2014;124:1069–1074. [DOI] [PubMed] [Google Scholar]
  • 17.Wei S, Fraser W, Luo Z. Inflammatory cytokines and spontaneous preterm birth in asymptomatic women: A systematic review. Obstet Gynecol. 2010;116:393–401. [DOI] [PubMed] [Google Scholar]
  • 18.Kramer MS, Lydon J, Goulet L, et al. Maternal Stress/Distress, Hormonal Pathways and Spontaneous Preterm Birth. Paediatr Perinat Epidemiol. 2013;27:237–246. [DOI] [PubMed] [Google Scholar]
  • 19.DiGiulio DB, Callahan BJ, McMurdie PJ, Costello EK, Lyell DJ, Robaczewska A, et al. Temporal and spatial variation of the human microbiota during pregnancy. Proceedings of the National Academy of Sciences. 2015;112:11060–11065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Christian LM. Psychoneuroimmunology in pregnancy: Immune pathways linking stress with maternal health, adverse birth outcomes, and fetal development. Neurosci Biobehav Rev. 2012;36:350–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Dunkel Schetter C Psychological science on pregnancy: stress processes, biopsychosocial models, and emerging research issues. Annu Rev Psychol. 2011;62:531–58. [DOI] [PubMed] [Google Scholar]
  • 22.Wadhwa PD, Entringer S, Buss C, Lu MC. The contribution of maternal stress to preterm birth: issues and considerations. Clin Perinatol. 2011;38:351–84 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Coussons-Read ME, Lobel M, Carey JC, Kreither MO, D'Anna K, Argys L, et al. The occurrence of preterm delivery is linked to pregnancy-specific distress and elevated inflammatory markers across gestation. Brain Behav Immun. 2012;26(4):650–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Peterson GF, Espel EV, Davis EP, Sandman CA, Glynn LM. Characterizing prenatal maternal distress with unique prenatal cortisol trajectories. Health Psychol. 2020. Nov;39(11):1013–1019. doi: 10.1037/hea0001018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Sandman CA. Prenatal CRH: An integrating signal of fetal distress. Dev Psychopathol. 2018. Aug;30(3):941–952. [DOI] [PubMed] [Google Scholar]
  • 26.Ramos IF, Guardino CM, Mansolf M, Glynn LM, Sandman CA, Hobel CJ, et al. Pregnancy anxiety predicts shorter gestation in Latina and non-Latina white women: The role of placental corticotrophin-releasing hormone. Psychoneuroendocrinology. 2019. Jan;99:166–173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Swales DA, Grande LA, Wing DA, Edelmann M, Glynn LM, Sandman C, et al. Can Placental Corticotropin-Releasing Hormone Inform Timing of Antenatal Corticosteroid Administration? J Clin Endocrinol Metab. 2019. Feb 1;104(2):443–450. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Hoffman MC, Mazzoni SE, Wagner BD, Laudenslager ML, Ross RG. Measures of Maternal Stress and Mood in Relation to Preterm Birth. Obstet Gynecol. 2016. Mar;127(3):545–552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.National Center for Health Statistics, final natality data 2015–2018. [Google Scholar]
  • 30.Martin JA, Hamilton BE, Osterman MJK, Driscoll AK. Births: Final Data for 2018. [PubMed] [Google Scholar]
  • 31.Johnson S, Bobb J, Ito K, Johnson S, McAlexander T, Ross Z, et al. Ambient Fine Particulate Matter, Nitrogen Dioxide, and Preterm Birth in New York City. Environ Health Perspect. 2016;124:1283–1290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.National vital statistics reports; vol 64 no 12. Hyattsville, MD: National Center for Health Statistics. 2010. [Google Scholar]
  • 33.Luke S, Salihu HM, Alio AP, Mbah AK, Jeffers D, Berry EL, et al. Risk factors for major antenatal depression among low-income African American women. J Womens Health. 2009;18:1841–1846. [DOI] [PubMed] [Google Scholar]
  • 34.Melville JL, Gavin A, Guo Y, Fan M, Katon WJ. Depressive disorders during pregnancy: Prevalence and risk factors in a large urban sample. Obstet Gynecol. 2010;116:1064–1070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Blumenshine P, Egerter S, Barclay CJ, Cubbin C, Braveman PA. Socioeconomic disparities in adverse birth outcomes: A systematic review. Am J Prev Med. 2010;39(3):263–272. [DOI] [PubMed] [Google Scholar]
  • 36.Gennaro S, Shults J, Garry DJ. Stress and preterm labor and birth in black women. J Obstet Gynecol Neonatal Nurs. 2008;37:538–545. [DOI] [PubMed] [Google Scholar]
  • 37.Bryant AS, Worjoloh A, Caughey AB, Washington AE. Racial/ethnic disparities in obstetric outcomes and care: Prevalence and determinants. Obstet Gynecol. 2010;202(4):335–343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Jallo N, Elswick R, Kinser P, Masho S, Price S, Svikis D. Prevalence and Predictors of Depressive Symptoms in Pregnant African American Women. Issues Ment Health Nurs. 2015;36:860–869. [DOI] [PubMed] [Google Scholar]
  • 39.Canady RB, Bullen BL, Holzman C, Broman C, Tian Y. Discrimination and symptoms of depression in pregnancy among African American and White women. Womens Health Issues. 2008;18(4):292–300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Grobman WA, Parker CB, Willinger M, Wing DA, Silver RM, Wapner RJ, et al. Racial Disparities in Adverse Pregnancy Outcomes and Psychosocial Stress. Obstetrics & Gynecology. 2018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Grote NK, Bridge JA, Gavin AR, Melville JL, Iyengar S, Katon WJ. A meta-analysis of depression during pregnancy and the risk of preterm birth, low birth weight, and intrauterine growth restriction. Arch Gen Psychiatry. 2010;67(10):1012–1024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Louis JM, Menard MK, Gee RE. Racial and ethnic disparities in maternal morbidity and mortality. Obstet Gynecol. 2015;125(3):690–694. [DOI] [PubMed] [Google Scholar]
  • 43.Elovitz MA, Gajer P, Riis V, Brown AG, Humphrys MS, Holm JB, et al. Cervicovaginal microbiota and local immune response modulate the risk of spontaneous preterm delivery. Nat Commun. 2019. Mar 21;10(1):1305. doi: 10.1038/s41467-019-09285-9. PMID: 30899005; PMCID: PMC6428888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Cohen S, Kamarck T, Mermelstein R. A global measure of perceived stress. J Health Soc Behav. 1983;24(4):385–396. [PubMed] [Google Scholar]
  • 45.Solivan AE, Xiong X, Harville EW, Buekens P. Measurement of Perceived Stress Among Pregnant Women: A Comparison of Two Different Instruments. Matern Child Health J. 2015;19(9):1910–1915. doi: 10.1007/s10995-015-1710-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Natamba BK, Achan J, Arbach A, Oyok TO, Ghosh S, Mehta S, et al. Reliability and validity of the center for epidemiologic studies-depression scale in screening for depression among HIV-infected and -uninfected pregnant women attending antenatal services in northern Uganda: a cross-sectional study. BMC Psychiatry. 2014. Nov 22;14:303. doi: 10.1186/s12888-014-0303-y. PMID: 25416286; PMCID: PMC4260190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Burris HH, Riis VM, Schmidt I, Gerson KD, Brown A, Elovitz MA. Maternal stress, low cervicovaginal β-defensin, and spontaneous preterm birth. Am J Obstet Gynecol MFM. 2020;2(2):100092. doi: 10.1016/j.ajogmf.2020.100092 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Silveira ML, Pekow PS, Dole N, Markenson G, Chasan-Taber L. Correlates of high perceived stress among pregnant Hispanic women in western Massachusetts. Matern Child Health J. 2013;17(6):1138–1150. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Hobel CJ, Goldstein A, Barrett ES. Psychosocial stress and pregnancy outcome. Clin Obstet Gynecol. 2008;51:333–48. [DOI] [PubMed] [Google Scholar]
  • 50.Liu L, Setse R, Grogan R, Powe NR, Nicholson WK. The effect of depression symptoms and social support on black-white differences in health-related quality of life in early pregnancy: The health status in pregnancy (HIP) study. BMC Pregnancy Childbirth. 2013;13:125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Forde A, Crookes D, Suglia S, & Demmer R (2019). The weathering hypothesis as an explanation for racial disparities in health: a systematic review. Annals of Epidemiology, 33, 1–18.e3. 10.1016/j.annepidem.2019.02.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Geronimus AT. (1992). The weathering hypothesis and the health of African-American women and infants: evidence and speculations. Ethnicity & Disease. Summer;2(3):207–21. PMID: 1467758 [PubMed] [Google Scholar]
  • 53.Holzman C, Eyster J, Kleyn M, Messer LC, Kaufman JS, Laraia BA et al. Maternal Weathering and Risk of Preterm Delivery. Am J Pub Health 2009; 99, 1864–1871, 10.2105/AJPH.2008.151589 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Witt WP, Wisk LE, Cheng ER, Hampton JM, Hagen EW. Preconception Mental Health Predicts Pregnancy Complications and Adverse Birth Outcomes: A National Population-Based Study. Matern Child Health J. 2012;2011;16:1525–1541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Clout D, Brown R. Sociodemographic, pregnancy, obstetric, and postnatal predictors of postpartum stress, anxiety and depression in new mothers. J. Affect. Disord 2015;188:60–67. [DOI] [PubMed] [Google Scholar]
  • 56.Collins JW, David RJ, Symons R, Handler A, Wall SN, Dwyer L. Low-Income African-American Mothers' Perception of Exposure to Racial Discrimination and Infant Birth Weight. Epidemiology. 2000;11:337–339. [DOI] [PubMed] [Google Scholar]
  • 57.Borders AE, Wolfe K, Qadir S, Kim KY, Holl J, Grobman W. Racial/ethnic differences in self-reported and biologic measures of chronic stress in pregnancy. J Perinatol. 2015;35(8):580–584. doi: 10.1038/jp.2015.18 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Chow A, Dharma C, Chen E, Mandhane PJ, Turvey SE, Elliot SJ, et al. Trajectories of Depressive Symptoms and Perceived Stress From Pregnancy to the Postnatal Period Among Canadian Women: Impact of Employment and Immigration. Am J Public Health. 2019;109(S3):S197–S204. doi: 10.2105/AJPH.2018.304624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Screening for perinatal depression. Committee Opinion No. 630. American College of Obstetricians and Gynecologists. Obstet Gynecol 2015;125:1268–71. [DOI] [PubMed] [Google Scholar]

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