Placental Histomorphological Alterations Associated with Excessive Gestational Weight Gain

Authors

Abstract

Background: Excessive gestational weight gain has been associated with adverse pregnancy outcomes and placental dysfunction. However, the histopathological alterations occurring in placental tissue under these conditions have not been fully elucidated. This study aimed to evaluate placental histomorphological changes in women with excessive gestational weight gain.

Methods: Placental tissues were obtained from healthy pregnant women and women with excessive gestational weight gain. Histopathological evaluation was performed using hematoxylin and eosin staining. Villous architecture, trophoblastic morphology, stromal organization, syncytial knot formation, and fibrinoid deposition were examined and compared between groups.

Results: Control placentas demonstrated preserved villous architecture, regular syncytiotrophoblast morphology, well-organized stromal structures, and minimal fibrinoid deposition and syncytial knot formation. In contrast, placentas from women with excessive gestational weight gain exhibited disrupted villous architecture, trophoblastic thickening, stromal edema and vacuolization, increased syncytial knot formation, fibrinoid deposition, and degenerative villous changes. These alterations were accompanied by impaired cellular organization and reduced structural integrity of the villi.

Conclusion: Excessive gestational weight gain is associated with significant placental histopathological alterations, including villous degeneration, stromal edema, trophoblastic thickening, increased syncytial knot formation, and fibrinoid deposition. These findings suggest that excessive maternal weight gain may adversely affect placental structure and potentially compromise placental function.

Keywords: Placenta; excessive gestational weight gain; histopathology; villous degeneration; pregnancy.

Keywords:

Placenta, excessive gestational weight gain, histopathology, villous degeneration, pregnancy

DOI

https://doi.org/10.22270/jddt.v16i8.7872

Author Biographies

Ayşe Yıldız , Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Murat Akkuş , Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Fırat Aşır , Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Department of Histology and Embryology, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Serhat Ege , Department of Gynecology and Obstetrics, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

Department of Gynecology and Obstetrics, Medical Faculty, Dicle University, 21280, Diyarbakır, Turkey.

References

1. Deputy NP, Sharma AJ, Kim SY, Hinkle SN. Prevalence and characteristics associated with gestational weight gain adequacy. Obstetrics & Gynecology. 2015;125(4):773–81.

2. Goławski K, Giermaziak W, Ciebiera M, Wojtyła C. Excessive Gestational Weight Gain and Pregnancy Outcomes. J Clin Med. 2023;12(9).

3. Kelly AC, Powell TL, Jansson T. Placental function in maternal obesity. Clin Sci (Lond). 2020;134(8):961–84.

4. O'Brien K, Wang Y. The placenta: a maternofetal interface. Annual Review of Nutrition. 2023;43(1):301–25.

5. Burton GJ, Fowden AL. The placenta: a multifaceted, transient organ. Philosophical Transactions of the Royal Society B: Biological Sciences. 2015;370(1663):20140066.

6. Sferruzzi‐Perri AN, Sandovici I, Constancia M, Fowden AL. Placental phenotype and the insulin‐like growth factors: resource allocation to fetal growth. The Journal of physiology. 2017;595(15):5057–93.

7. Roland CS, Hu J, Ren C-E, Chen H, Li J, Varvoutis MS, et al. Morphological changes of placental syncytium and their implications for the pathogenesis of preeclampsia. Cellular and molecular life sciences. 2016;73(2):365–76.

8. Yükselmiş Ö, Akkuş M, Aşır F. Histopathological Evaluation of Placental Changes in Women with Excessive Gestational Weight Gain. Journal of Drug Delivery & Therapeutics. 2026;16(2):164.

9. Akdeniz AS, Acar GEA, Türe Z, Aşır A, Akdeniz O, Aktaş A, et al. Homeobox A1 Expression in Diabetic Pregnancy: Immunohistochemical and Computational Perspectives. Harran Üniversitesi Tıp Fakültesi Dergisi. 2025;22(2):265–71.

10. Yıldırım E, Aydeniz Acar GE, Türe Z, Aşır A, Aşır F, Korak T, et al. Investigation of M3 muscarinic acetylcholine receptor expression in placentas of smoking women. Perinatal Journal. 2025;33(2):1–8.

11. Acar GEA, Akdeniz AS, Türe Z, Aşır A, Acar M, Aşır F, et al. HOXA1 expression in placentas of woman with fetal growth restriction. Perinatal Journal. 2024;32(2):166–72.

12. Türe Z, Akdeniz AS, Acar GEA, Aşır F, Korak T, Ege S. HOXA1 Expression in preeclampsia: immunohistochemical and bioinformatic analyses. Perinatal Journal. 2025;33(1):11–7.

13. Desoye G, Carter AM. Fetoplacental oxygen homeostasis in pregnancies with maternal diabetes mellitus and obesity. Nature Reviews Endocrinology. 2022;18(10):593–607.

14. Beneventi F, Bellingeri C, De Maggio I, Cavagnoli C, Fumanelli S, Ligari E, et al. Placental pathologic features in obesity. Placenta. 2023;144:1–7.

15. Jauniaux E, Hussein AM, Elbarmelgy RM, Elbarmelgy RA, Burton GJ. Failure of placental detachment in accreta placentation is associated with excessive fibrinoid deposition at the utero-placental interface. American journal of obstetrics and gynecology. 2022;226(2):243. e1–. e10.

16. Khong TY, Mooney EE, Ariel I, Balmus NC, Boyd TK, Brundler M-A, et al. Sampling and definitions of placental lesions: Amsterdam placental workshop group consensus statement. Archives of pathology & laboratory medicine. 2016;140(7):698–713.

17. Kelly AC, Powell TL, Jansson T. Placental function in maternal obesity. Clinical Science. 2020;134(8):961–84.

18. Calleja-Agius J, Muttukrishna S, Jauniaux E. The role of tumor necrosis factor-receptors in pregnancy with normal and adverse outcome. International Journal of Interferon, Cytokine and Mediator Research. 2012:1–15.

19. Nevo O, Soleymanlou N, Wu Y, Xu J, Kingdom J, Many A, et al. Increased expression of sFlt-1 in in vivo and in vitro models of human placental hypoxia is mediated by HIF-1. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 2006;291(4):R1085–R93.

20. Bobek G, Surmon L, Mirabito KM, Makris A, Hennessy A. Placental regulation of inflammation and hypoxia after TNF‐α infusion in mice. American journal of reproductive immunology. 2015;74(5):407–18.

Published

2026-08-16
Statistics
Abstract Display: 44
PDF Downloads: 43
PDF Downloads: 8

How to Cite

1.
Yıldız A, Akkuş M, Aşır F, Ege S. Placental Histomorphological Alterations Associated with Excessive Gestational Weight Gain. J. Drug Delivery Ther. [Internet]. 2026 Aug. 16 [cited 2026 Aug. 30];16(8):83-8. Available from: https://www.jddtonline.info/index.php/jddt/article/view/7872

How to Cite

1.
Yıldız A, Akkuş M, Aşır F, Ege S. Placental Histomorphological Alterations Associated with Excessive Gestational Weight Gain. J. Drug Delivery Ther. [Internet]. 2026 Aug. 16 [cited 2026 Aug. 30];16(8):83-8. Available from: https://www.jddtonline.info/index.php/jddt/article/view/7872