Early postpartum cortisol and malondialdehyde trajectories in non-depressed mothers: A pilot study in Surabaya, Indonesia
##plugins.themes.bootstrap3.article.main##
Abstract
The days immediately following childbirth are characterized by rapid biological and psychological changes. Stress and oxidative biomarkers cortisol and malondialdehyde (MDA) in particular have been implicated in postpartum mood disturbance. However, their early postpartum trajectories in healthy, non-depressed mothers, particularly in the Indonesia context, remain poorly documented. This pilot study therefore investigated changes in cortisol and MDA levels during the first three days postpartum women in Surabaya, Indonesia. A quantitative time-series study was conducted at the Surabaya, Indonesia. Thirty postpartum mothers were assessed on day 1 and day 3 after delivery. Serum cortisol and MDA levels were measured using ELISA and TBARS methods. Depressive symptoms were evaluated using the Edinburgh Postnatal Depression Scale (EPDS) and analyzed as a continuous variable. Data were tested for normality and homogeneity, followed by paired comparisons and correlation analyses. No significant differences were observed in cortisol (p-value = 0.900) and MDA levels on day 1 and day 3 (p-value = 0.211). EPDS scores decreased from 9.80 ± 3.21 to 8.00 ± 4.46, but not statistically significant (p-value = 0.244). A significant moderate positive correlation was found between cortisol levels and EPDS scores on day 1 (r = 0.519; p-value = 0.003), but not on day 3. Meanwhile, no significant relationship was found between MDA and EPDS scores. Maintained cortisol and MDA levels after 3 days postpartum may reflect normal recovery patterns in mothers without depression. These findings provide a basic for further research and support the development of integrated psychosocial and biological screening strategies, in line with SDG 3 (Healthy Lives and Well-being).
Downloads
##plugins.themes.bootstrap3.article.details##
Copyright (c) 2026 Hinda Novianti, Nety Mawarda Hatmanti, Uliyatul Laili, Ary Andini, Norhaini Majid

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
References
1. Wang Z, Liu J, Shuai H, Cai Z, Fu X, Liu Y, Xiao X, Zhang W, Krabbendam E, Liu S, Liu Z, Li Z, Yang BX. Mapping global prevalence of depression among postpartum women. Transl Psychiatry. 2021;11(1):543. https://doi.org/10.1038/s41398-021-01663-6
2. Weiss SJ, Xu L. Postpartum symptoms of anxiety, depression and stress: Differential relationships to women’s cortisol profiles. Arch Womens Ment Health. 2024;27(3):435–445. https://doi.org/10.1007/s00737-024-01421-9
3. Rinne GR, Guardino CM, Soriano M, Dunkel Schetter C. Chronic stress and hair cortisol concentration in mothers: A two‐study investigation. Stress and Health. 2024;40(6): e3493. https://doi.org/10.1002/smi.3493
4. Yuan C, Li H, Zhang M, Wang Z, Dong J, Cui L, Guo L, Liu K, Li J, Wang H. Selenium yeast alleviates Escherichia coli-induced endometritis in goats under high cortisol background. Animals. 2025;15(5):693. https://doi.org/10.3390/ani15050693
5. Zhang K, He L, Li Z, Ding R, Han X, Chen B, Cao G, Ye JH, Li T, Fu R. Bridging neurobiological insights and clinical biomarkers in postpartum depression: A narrative review. Int J Mol Sci. 2024;25(16):8835. https://doi.org/10.3390/ijms25168835
6. Jain P, Chauhan AK, Singh K, Garg R, Jain N, Singh R. Correlation of perceived stress with monthly cyclical changes in the female body. J Family Med Prim Care. 2023;12(11):2927–33. https://doi.org/10.4103/jfmpc.jfmpc_874_23
7. Thompson SF, Shimomaeda L, Calhoun R, Metje A, Nurius PS, Whiley DJ, Lengua LJ. Biological and social cascades of prenatal contextual risk and maternal psychological distress to early-childhood adjustment. Dev Psychol. 2024;60(9):1593–605. https://doi.org/10.1037/dev0001759
8. Kanekasu H, Shiraiwa Y, Taira S, Watanabe H. Primiparas’ prenatal depressive symptoms, anxiety, and salivary oxytocin level predict early postnatal maternal–infant bonding: a Japanese longitudinal study. Arch Womens Ment Health. 2024;27(4):649–58. https://doi.org/10.1007/s00737-024-01441-5
9. Hicks LE, Yeo S. Longitudinal changes of depressive symptoms in sedentary women who exercised during pregnancy. Women’s Health Rep. 2023;4(1):523–30. https://doi.org/10.1089/whr.2023.0028
10. Pan X, Chen Y, Chen C, Chen J, Wang J, Chen Y, Zhang W, Wu J, Liu W, Zou Z, Zhu L, Chen X. Dual trajectory of insomnia and depressive symptoms in women from early pregnancy to 6 months postpartum: a prospective cohort study. BMC Pregnancy Childbirth. 2025;25(1):582. https://doi.org/10.1186/s12884-025-07649-2
11. Aprilia D, Noer AH, Ninin RH, Hinduan ZR. Socio-cultural experiences of exclusive breastfeeding among Banjar mothers in Indonesia. Healthcare (Basel). 2026;14(14):2110. https://doi.org/10.3390/healthcare14142110
12. Rathi A, Khapre S, Chavada J, Gupta S, Singla T. Postpartum depression and its biological biomarkers. Cureus. 2022;14(11):e31124. https://doi.org/10.7759/cureus.31124
13. Frndak S, Syed S, Saleh J, Kocher M, Wen X. Prenatal predictors of postpartum depression trajectories from birth to 24 months amongst smoking women. J Clin Nurs. 2022;31(11–12):1643–53. https://doi.org/10.1111/jocn.16019
14. Nguyen MQ, Munakata K, Natsume M, Nakamura Y, Miyabayashi H, Nagano N, Morioka I. The Influence of maternal diet in late pregnancy on malondialdehyde and cortisol levels in maternal and cord blood. Nutrients. 2025;17(6):1077. https://doi.org/10.3390/nu17061077
15. Wang X, Zhong X. Molecular effects of digital psychological intervention for perinatal stress: Cell culture, animal model validation, and machine learning-based biomarker identification. Sci Rep. 2026;16(1):2127. https://doi.org/10.1038/s41598-025-31813-5
16. Wen L, Li R, Wang J, Yi J. The reproductive stress hypothesis. Reproduction. 2019;158(6):R209–R218. https://doi.org/10.1530/REP-18-0592
17. Seth S, Lewis AJ, Galbally M. Perinatal maternal depression and cortisol function in pregnancy and the postpartum period: A systematic literature review. BMC Pregnancy Childbirth. 2016;16(1):124. https://doi.org/10.1186/s12884-016-0915-y
18. Iliadis SI, Comasco E, Sylvén S, Hellgren C, Sundström Poromaa I, Skalkidou A. Prenatal and postpartum evening salivary cortisol levels in association with peripartum depressive symptoms. PLoS One. 2015;10(8):e0135471. https://doi.org/10.1371/journal.pone.0135471
19. El Sherbiny S, Squillacioti G, Colombi N, Ghelli F, Lenta E, Dalla Costa C, Bono R. The effect of dietary patterns and nutrient intake on oxidative stress levels in pregnant women: A systematic review. Nutrients. 2025;17(6):1077. https://doi.org/10.3390/antiox12071427
20. Modzelewski S, Oracz A, Iłendo K, Sokół A, Waszkiewicz N. Biomarkers of postpartum depression: a narrative review. J Clin Med. 2023;12(20):6519. https://doi.org/10.3390/jcm12206519
21. Han VX, Patel S, Jones HF, Nielsen TC, Mohammad SS, Hofer MJ, Gold W, Brilot F, Lain SJ, Nassar N, Dale RC. Maternal acute and chronic inflammation in pregnancy is associated with common neurodevelopmental disorders: A systematic review. Transl Psychiatry. 2021;11(1):71. https://doi.org/10.1038/s41398-021-01198-w
22. Wu XS, Yousif L, Miles A, Braakhuis A. A comparison of dietary intake and nutritional status between aged care residents consuming texture-modified diets with and without oral nutritional supplements. Nutrients. 2022;14(3):669. https://doi.org/10.3390/nu14030669
23. Sobol M, Hryhorchuk I, Plucińska E, Szczepaniak P, Błachnio A, Stasiniewicz J, Sobol MK. The effect of cortisol in early pregnancy on postpartum depressive symptoms. Sci Rep. 2025;15(1):13108. https://doi.org/10.1038/s41598-025-88772-0
Hinda Novianti
https://orcid.org/0000-0002-4012-3721
Ary Andini
Norhaini Majid