Peripartum mood disturbances overview
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sunita Kumawat, M.B.B.S[2]
Overview
Childbirth is a life changing event in a woman's life. Her body undergoes many physiological and psychological changes during pregnancy and childbirth; a causal relationship between hormone changes and mood shifts has been proposed. During the postpartum period, women face many depressive symptoms which varies in severity from mild postpartum blues to serious mood disorders like postpartum depression and postpartum psychosis. Identification and treatment of these mood disorders is critical to both child and mother's health.
Historical Perspective
In 460 B.C., Hippocrates was the first to mention about postpartum fever, mania, delirium and agitation. His writings reflected how postpartum depression is described today.[1]
In 11th century, a professor of medicine, Trotula of Salerno, first recognized postpartum depression.
In 1547, a Portuguese physician, Joao Rodrigues de Castello Branco(Amatus Lusitanus), briefly described postpartum depression.
Between 16th and 18th centuries about 50 brief reports about Psychosis were published stating that these psychoses were recurrent and could be seen in both non-lactating and lactating females.[2]
In 1797, Osiander, an obstetrician, wrote about 2 cases in detail, that are among the treasures for postpartum psychosis.
In 1819, Esquiro evaluated inpatients in the Salpêtrière, which paved the way for long term research.
Classification
Puerperal psychiatric illnesses may be classified according to Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-V) into 3 types:
- postpartum blues,
- postpartum depression, and
- postpartum psychosis.
During the postpartum period there is also increased susceptibility to anxiety disorders such as obsessive-compulsive disorder and panic disorder. [3]
Pathophysiology
Many pathological mechanisms are involved in postpartum depression which interact with one another.[4]
- Genetics of postpartum depression
Estrogen receptor alpha gene, polymorphisms in the serotonin transporter gene, 5-HTT, and the gene encoding for MAOA and the gene encoding for Catechol-O-methyltransferase (COMT), Genetic variants for the TPH2 gene, a SNP in OXT was predictive of both variation in breastfeeding duration and postpartum depression scores, an interaction between a SNP in the OXTR gene and methylation state was detected in association with postpartum depression. In a genome-wide linkage and association study, the Hemicentin 1 gene (HMNC1) had the strongest association with postpartum depression.
- Epigenetic mechanisms of postpartum depression
In women with postpartum depression, there was a substantial interaction between OXTR DNA methylation, estradiol, and the ratio of allopregnanolone to progesterone. Alterations in DNA methylation of the OXTR gene are adversely linked with blood estradiol levels in women with postpartum depression. As a result, epigenetic alterations can affect metabolic processes linked to postpartum depression.
- Neuroendocrine mechanisms of postpartum depression
In postpartum depression, there is an interaction between the Hypothalamus-pituitary-gonadal (HPG) and Hypothalamus-Pituitary-Adrenal(HPA) axis. HPA axis function has been found to be influenced by reproductive hormones and vice versa. As a result, any change in reproductive hormones may cause stress hormone levels to fluctuate, resulting in postpartum depression. Alterations of the HPA axis' function may also affect reproductive hormone levels, contributing to postpartum depression.
- Neurotransmitters and postpartum depression
GABA-GABA which is an inhibitory neurotransmitter in the brain, its level is inversely related with the depression symptoms in the postpartum period.
Glutamate-Glutamate is the excitatory neurotransmitter in the brain. In women with postpartum depression its level are increased in the medial prefrontal cortex and decreased in the dorsolateral prefrontal cortex.
Serotonin-The binding of Serotonin to 5HT1A receptors is decreased in the mesiotemporal and anterior cingulate cortices.
Dopamine-Mutations in DR1 is related to the behaviour of mother paying less attention to the baby.
- Neuroinflammatory mechanisms in postpartum depression
There is a negative relationship between T-cell number and postpartum depression symptoms, whereas IL-6 and IL-1β have a significant positive relationship with it.
It is thought that in postpartum psychosis, immunoneuroendocrine set point is dysregulated with overactivation of the immune system's macrophage and monocyte arm. [5]
Causes
Postpartum depression: drop in estrogen, progesterone and thyroid hormones after the birth of the child, anxiety, lack of sleep , distorted self image :[6]
postpartum psychosis: sleep disruptions, genetics, immune system dysregulation, family history of mental health conditions, presence of other underlying mental health conditions, extreme hormone fluctuations, thyroid gland dysfunction [7]
Postpartum blues: are caused mainly by a drop in estrogen and progesterone post delivery, decrease in thyroid hormone, sleep deprivation, not eating properly, emotional issues, anxiety about the care of the newborn and not finding time for oneself.
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References
- ↑ "PayPerView: A Historical Perspective on the Psychiatry of Motherhood - Karger Publishers".
- ↑ "postpartum-psychosis".
- ↑ "Epidemiology and Phenomenology of Postpartum Mood Disorders | Psychiatric Annals".
- ↑ Payne JL, Maguire J (January 2019). "Pathophysiological mechanisms implicated in postpartum depression". Front Neuroendocrinol. 52: 165–180. doi:10.1016/j.yfrne.2018.12.001. PMC 6370514. PMID 30552910.
- ↑ Davies W (June 2017). "Understanding the pathophysiology of postpartum psychosis: Challenges and new approaches". World J Psychiatry. 7 (2): 77–88. doi:10.5498/wjp.v7.i2.77. PMC 5491479. PMID 28713685.
- ↑ "Postpartum Depression: Symptoms, Causes, Risks, Types, Tests, Professional and Self-Care".
- ↑ "What Is Postpartum Psychosis? Causes, Symptoms & More | Psych Central".