4.6 Article

Growth differentiation factor 15 increases in both cerebrospinal fluid and serum during pregnancy

期刊

PLOS ONE
卷 16, 期 5, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0248980

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资金

  1. Swedish Research Council [12206, 2017-00915, VR-2017-01409, 2018-02532]
  2. Swedish Diabetes Association Research Foundation [2015-08]
  3. Swedish government
  4. ALF [720851, 715986, 720931, ALFGBG-722491]
  5. Alzheimer Drug Discovery Foundation (ADDF), USA [RDAPB-201809-2016615, 201809-2016862]
  6. Swedish Alzheimer Foundation [AF-742881]
  7. Swedish brain foundation [FO2017-0243, FO2019-0270]
  8. European Union Joint Program for Neurodegenerative Disorders [JPND2019-466-236]
  9. European Research Council [681712]
  10. Emil and Wera Cornell Foundation
  11. Ahlen Foundation

向作者/读者索取更多资源

The study found that levels of GDF15 in both cerebrospinal fluid (CSF) and serum increase significantly during pregnancy, with the increase potentially being related to the sex of the fetus.
Aim Growth differentiation factor 15 (GDF15) increases in serum during pregnancy to levels not seen in any other physiological state and is suggested to be involved in pregnancy-induced nausea, weight regulation and glucose metabolism. The main action of GDF15 is regulated through a receptor of the brainstem, i.e., through exposure of GDF15 in both blood and cerebrospinal fluid (CSF). The aim of the current study was to measure GDF15 in both CSF and serum during pregnancy, and to compare it longitudinally to non-pregnant levels. Methods Women were sampled at elective caesarean section (n = 45, BMI = 28.15.0) and were followed up 5 years after pregnancy (n = 25). GDF15, insulin and leptin were measured in CSF and serum. Additional measurements included plasma glucose, and serum adiponectin and Hs-CRP. Results GDF15 levels were higher during pregnancy compared with follow-up in both CSF (385 +/- 128 vs. 115 +/- 32 ng/l, P<0.001) and serum (73789 +/- 29198 vs. 404 +/- 102 ng/l, P<0.001). CSF levels correlated with serum levels during pregnancy (P<0.001), but not in the non-pregnant state (P = 0.98). Both CSF and serum GDF15 were highest in women carrying a female fetus (P<0.001). Serum GDF15 correlated with the homeostatic model assessment for beta-cell function and placental weight, and CSF GDF15 correlated inversely with CSF insulin levels. Conclusion This, the first study to measure CSF GDF15 during pregnancy, demonstrated increased GDF15 levels in both serum and CSF during pregnancy. The results suggest that effects of GDF15 during pregnancy can be mediated by increases in both CSF and serum levels.

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