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. 2025 Mar 13;8(3):e250743. doi: 10.1001/jamanetworkopen.2025.0743

Prenatal Depression and Symptom Severity by Maternal Race and Ethnicity

Kendria Kelly-Taylor 1,, Sara Aghaee 1, Joshua Nugent 1, Nina Oberman 1, Ai Kubo 1, Elaine Kurtovich 1, Charles P Quesenberry Jr 1, Ayesha C Sujan 2, Kathryn Erickson-Ridout 1,3, Mibhali M Bhalala 4, Lyndsay A Avalos 1,5
PMCID: PMC11907315  PMID: 40080023

Abstract

This cross-sectional study compares the prevalence and risk for diagnosed and undiagnosed prenatal depression among pregnant individuals of different races and ethnicities.

Introduction

Prenatal depression has been associated with adverse outcomes, including preterm birth and postpartum depression, and disproportionately affects racial or ethnic minoritized pregnant individuals. Black, Hispanic, and Asian individuals may experience more severe depression symptoms yet be less likely to engage in treatment, possibly due to clinical underdiagnosis.1 Prior research has often aggregated racial and ethnic groups, potentially masking important within-group differences and cultural nuances.2 To address these gaps, we examined differences in prenatal depression diagnoses (PDDs), self-reported symptoms of moderate to severe depression, and undiagnosed depression among a large cohort of racially and ethnically diverse pregnant individuals screened for depression.3

Methods

This population-based cross-sectional study was conducted among Kaiser Permanente Northern California (KPNC) members aged 15 to 45 years with a singleton live birth (January 1, 2013-December 31, 2019) who had at least 1 KPNC prenatal care visit and self-reported race and ethnicity data. KPNC and California State Institutional Review Boards approved this study and waived informed consent because patient privacy and records confidentiality requirements were met. We followed the STROBE reporting guideline.

Race and ethnicity were ascertained from California State birth records and KPNC databases. Twenty racial and ethnic groups were identified for analysis (Figure). PDD and moderate to severe depression symptoms were defined using International Classification of Diseases, Ninth Revision and International Statistical Classification of Diseases and Related Health Problems, Tenth Revision codes and a Patient Health Questionnaire–9 (PHQ-9) score of 10 or higher,4 respectively, during pregnancy. Undiagnosed depression was identified as a PHQ-9 score of 10 or higher without evidence of depression diagnosis.

Figure. Risk of Prenatal Depression Diagnosis, Moderate to Severe Depression Symptoms, and Undiagnosed Depression.

Figure.

Error bars represent 95% CIs. aRR indicates adjusted relative risk.

aAdjusted for maternal age, parity, and delivery year.

bAmong sample with moderate to severe depression.

Modified Poisson regression models with robust SEs were used to estimate relative risk (RR) of each study outcome associated with racial and ethnic subgroups, adjusted for a priori–specified confounders (maternal age, parity, delivery year). Analyses were conducted from December 2023 to August 2024, using SAS 9.4 (SAS Institute).

Results

Among 258 452 participants (maternal mean [SD] age, 30.7 [5.3] years), PDD prevalence was 15.5% and prevalence of moderate to severe depressive symptoms was 10.9% (Table). Within subgroups, prevalence ranged from 4.7% (Hmong) to 26.7% (Puerto Rican) for PDD and from 7.5% (Japanese) to 17.3% (Black) for symptoms (Figure). Compared with White individuals, Puerto Rican (adjusted RR [aRR], 1.28; 95% CI, 1.17-1.39) and Black (aRR, 1.03; 95% CI, 1.01-1.07) individuals had significantly higher risk of PDD. Significantly lower PDD risk was observed among Asian and Pacific Islander (Vietnamese: aRR, 0.25; 95% CI, 0.24-0.30), Mexican (aRR, 0.75; 95% CI, 0.73-0.77), and Central and South American (aRR, 0.82; 95% CI, 0.78-0.87) individuals compared with White individuals (Figure).

Table. Characteristics of Pregnant Individuals in Kaiser Permanente Northern California between January 1, 2013, and December 31, 2019.

Characteristic Participants, No. (%) (N = 258 452)
Race and ethnicity
American Indian or Alaska Native 537 (0.2)
Asian and Pacific Islander
Asian Indian 16 210 (6.3)
Cambodian 1157 (0.5)
Chinese 16 010 (6.2)
Filipino 15 267 (5.9)
Hawaiian or Pacific Islander 1919 (0.7)
Hmong 2996 (1.2)
Japanese 1289 (0.5)
Korean 2292 (0.9)
Laotian 684 (0.3)
Other South Asiana 1547 (0.6)
Other Southeast Asiana 529 (0.2)
Thai 603 (0.2)
Vietnamese 6178 (2.4)
Hispanic
Central and South American 8701 (3.4)
Mexican 57 060 (22.1)
Other Hispanica 7517 (2.9)
Puerto Rican 1535 (0.6)
Black 15 829 (6.1)
White 100 592 (39.0)
Prenatal depression diagnosisb
Yes 40 155 (15.5)
No 218 297 (84.5)
Depression severityc
None to mild 207 384 (80.2)
Moderate to severe 25 405 (10.9)
Missing data 25 663 (9.9)
Maternal age, y
15-24 38 702 (15.0)
25-29 70 894 (27.4)
30-34 93 056 (36.0)
35-45 55 800 (21.6)
Educational level
<High school diploma 7501 (2.9)
High school diploma or GED 39 845 (15.4)
Some college 72 145 (27.9)
Bachelor’s degree 68 762 (26.6)
Postgraduate 43 894 (17.0)
Missing data 26 305 (10.2)
Parity
0 113 684 (44.0)
1 89 411 (34.6)
≥2 53 705 (20.8)
Missing data 1652 (0.6)
Medicaid
No 233 336 (90.3)
Yes 25 116 (9.7)
NDI quartile
1 (least deprived) 64 793 (25.1)
2 64 578 (25.0)
3 64 326 (24.9)
4 (most deprived) 63 882 (24.7)
Missing data 873 (0.3)
Delivery year
2013 32 804 (12.7)
2014 34 665 (13.4)
2015 36 484 (14.1)
2016 37 855 (14.7)
2017 38 083 (14.7)
2018 38 349 (14.8)
2019 40 212 (15.6)

Abbreviations: GED, General Educational Development; NDI, Neighborhood Deprivation Index.

a

Other South Asian ethnicities included Pakistani, Nepalese, Sri Lankan, and Bangladeshi or Bengali. Other Southeast Asian ethnicities included Malaysian, Indonesian, Singaporean, and Burmese. Other Hispanic included ethnic groups in countries where the primary spoken language is Spanish.

b

Prenatal depression diagnosis was documented between the first day of the last menstrual period through the day before a live birth.

c

Depression severity was measured by Patient Health Questionnaire–9 (PHQ-9) and documented between the first day of the last menstrual period through the day before a live birth. PHQ-9 was administered to pregnant individuals as part of KPNC’s standard prenatal care at the first prenatal visit and at 26 to 28 weeks.3 None to mild depression symptoms were defined as PHQ-9 score of 0 to 9, and moderate to severe depression symptoms were defined as PHQ-9 score of 10 or higher; higher scores indicated more symptoms. A PHQ-9 score of 10 or higher is consistent with the clinical threshold for a depression diagnosis.4

Risk of moderate to severe depressive symptoms was significantly greater among all groups compared with White individuals, with increased risk ranging from 9% (Chinese: aRR, 1.09; 95% CI, 1.03-1.16) to 108% (Black: aRR, 2.08; 95% CI, 1.99-2.17) (Figure). Risk of undiagnosed depression was significantly higher across all groups with moderate to severe symptoms compared with White individuals, except American Indian or Alaska Native (aRR, 0.81; 95% CI, 0.57-1.15) and Puerto Rican (aRR, 0.83; 95% CI, 0.69-0.99) individuals. For Asian subgroups, aRR was generally higher than for Black or Hispanic individuals, with highest risk among Hmong individuals (aRR, 2.10; 95% CI, 2.00-2.21) (Figure).

Discussion

The findings underscore the importance of disaggregating race and ethnicity data, especially among Asian and Hispanic populations, to better understand PDD burden and symptom severity. Heterogeneity among Hispanic and Asian groups attributed to factors such as nativity (US-born vs non-US-born) and acculturation may contribute to intragroup disparities.5 The results also highlight higher risk of depression underdiagnosis among racial and ethnic groups, which may precede treatment-initiation disparities. To increase engagement, future research should explore how factors such as attitudes about mental illness, lack of cultural competence in health care settings, and residential segregation contribute to disparities.

KPNC’s diverse membership and PDD screening program capturing self-reported symptom severity strengthen this study. A study limitation is that findings may not be generalizable to uninsured pregnant individuals.

Supplement.

Data Sharing Statement

References

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Associated Data

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Supplementary Materials

Supplement.

Data Sharing Statement


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