TY - JOUR
T1 - Polyunsaturated fatty acids and inflammatory markers in major depressive episodes during pregnancy
AU - Chang, Jane Pei Chen
AU - Lin, Chih Ying
AU - Lin, Pan Yen
AU - Shih, Yin Hua
AU - Chiu, Tsan Hung
AU - Ho, Ming
AU - Yang, Hui Ting
AU - Huang, Shih Yi
AU - Gałecki, Piotr
AU - Su, Kuan Pin
N1 - Publisher Copyright:
© 2017 Elsevier Inc.
PY - 2018/1/3
Y1 - 2018/1/3
N2 - Introduction: Prenatal depression (PND) is a common psychiatric disorder in pregnant women and leads to psychosocial dysfunction, high suicidal rate, and adverse childcare. Patients with PND have omega-3 polyunsaturated fatty acid (omega-3 or n-3 PUFAs) deficits, which might link to chronic low-grade inflammatory process and the pathophysiological mechanisms of depression. In this case-control study, we examined the levels of PUFAs and inflammatory cytokines in PND. Method: Blood samples were obtained and analyzed from 16 healthy controls and 17 depressed cases (PND group) diagnosed with Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV). Independent sample t-test and correlation analysis were performed with Statistical Package for the Social Sciences (SPSS) logistics correlation analysis. Results: PND group had significantly lower levels of total n-3 (p = 0.026), docosahexaenoic acid (DHA) (p = 0.020) and eicosapentaenoic (EPA) (p = 0.019) but a higher omega-6 (n-6)/n-3 PUFAs ratio (p = 0.007) and tumor necrosis factor alpha (TNF-α) (p = 0.016) level. Moreover, the duration of current PND episodes were also significantly correlated with DHA, EPA, n-3 PUFAs, n-6/n-3 ratio and TNF-α. In terms of PUFAs and cytokine levels, only DHA was inversely correlated with TNF-α. Conclusion: PND is significantly associated with lower DHA, EPA, and total n-3 PUFAs levels and an increased n-6/n-3 PUFAs ratio, while the duration of PND is associated with lower levels of n-3 PUFAs, including DHA and EPA. The correlation of PUFAs levels with depression and TNF-α level grant further investigation into the inflammatory process underlying PND, mediated by PUFAs.
AB - Introduction: Prenatal depression (PND) is a common psychiatric disorder in pregnant women and leads to psychosocial dysfunction, high suicidal rate, and adverse childcare. Patients with PND have omega-3 polyunsaturated fatty acid (omega-3 or n-3 PUFAs) deficits, which might link to chronic low-grade inflammatory process and the pathophysiological mechanisms of depression. In this case-control study, we examined the levels of PUFAs and inflammatory cytokines in PND. Method: Blood samples were obtained and analyzed from 16 healthy controls and 17 depressed cases (PND group) diagnosed with Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV). Independent sample t-test and correlation analysis were performed with Statistical Package for the Social Sciences (SPSS) logistics correlation analysis. Results: PND group had significantly lower levels of total n-3 (p = 0.026), docosahexaenoic acid (DHA) (p = 0.020) and eicosapentaenoic (EPA) (p = 0.019) but a higher omega-6 (n-6)/n-3 PUFAs ratio (p = 0.007) and tumor necrosis factor alpha (TNF-α) (p = 0.016) level. Moreover, the duration of current PND episodes were also significantly correlated with DHA, EPA, n-3 PUFAs, n-6/n-3 ratio and TNF-α. In terms of PUFAs and cytokine levels, only DHA was inversely correlated with TNF-α. Conclusion: PND is significantly associated with lower DHA, EPA, and total n-3 PUFAs levels and an increased n-6/n-3 PUFAs ratio, while the duration of PND is associated with lower levels of n-3 PUFAs, including DHA and EPA. The correlation of PUFAs levels with depression and TNF-α level grant further investigation into the inflammatory process underlying PND, mediated by PUFAs.
KW - Inflammation
KW - Major depressive disorder
KW - Perinatal depression (PND)
KW - Polyunsaturated fatty acids (PUFAs)
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U2 - 10.1016/j.pnpbp.2017.05.008
DO - 10.1016/j.pnpbp.2017.05.008
M3 - Article
AN - SCOPUS:85019581830
SN - 0278-5846
VL - 80
SP - 273
EP - 278
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
ER -