SSRI antidepressant use during pregnancy may increase the risk of autism

Summary: The use of selective serotonin reuptake inhibitors (SSRIs, such as Prozac®, Celexa®, Lexapro®, Luvox® and Paxil®) taken during pregnancy—especially the first trimester—appears to increase the risk of autism spectrum disorders. There are evidence-based alternatives to SSRIs that support brain health without putting the fetus at risk.

A study recently published in the journal Archives of General Psychiatry draws attention to a risk of autism spectrum disorders (ASDs) born to mothers who took SSRI antidepressants during their pregnancy. The authors observe:

“The prevalence of autism spectrum disorders (ASDs) has increased over recent years. Use of antidepressant medications during pregnancy also shows a secular increase in recent decades, prompting concerns that prenatal exposure may contribute to increased risk of ASD.”

Therefore they set out to…

“…systematically evaluate whether prenatal exposure to antidepressant medications is associated with increased risk of ASD.”

In order to do so they compared the data for 298 children with ASD to 1507 randomly selected control children, along with the data for both their mothers. Their findings support a cautionary approach to the prenatal use of SSRIs:

“Prenatal exposure to antidepressant medications was reported for 20 case children (6.7%) and 50 control children (3.3%). In adjusted logistic regression models, we found a 2-fold increased risk of ASD associated with treatment with selective serotonin reuptake inhibitors by the mother during the year before delivery (adjusted odds ratio, 2.2), with the strongest effect associated with treatment during the first trimester (adjusted odds ratio, 3.8).”

In other words, the increase in risk for the whole year before delivery was 220%, but limiting the investigation to the first trimester it was 380%. Interestingly…

“No increase in risk was found for mothers with a history of mental health treatment in the absence of prenatal exposure to selective serotonin reuptake inhibitors.”

Meaning that it wasn’t a history of mental health treatment the year before delivery but specifically the use of SSRIs that accounted for the increased risk of ASDs. The authors conclude:

“Although the number of children exposed prenatally to selective serotonin reuptake inhibitors in this population was low, results suggest that exposure, especially during the first trimester, may modestly increase the risk of ASD. The potential risk associated with exposure must be balanced with the risk to the mother or fetus of untreated mental health disorders.”

This would be a troubling dilemma were it not for the fact that therapies supporting brain health are available to treat depression. Serotonin production and signaling, when indicated, can be supported in a physiological and sustainable manner that promotes the brain health of mother and fetus. A categorization and description of key resources that applies to adults as well as children is available in the Parents’ Guide To Brain Health.

Side effects of antidepressants are grossly underrecognized by psychiatrists

Journal of Clinical Psychiatry 2A study just published in The Journal of Clinical Psychiatry brings to light the extent to which the side effects of common antidepressant medications are not recognized or reported by psychiatrists. The authors state:

“Despite the clinical importance of detecting side effects, few studies have examined the adequacy of their detection and documentation by clinicians.”

The authors set out to compare the side effects recorded in the charts of three hundred depressed outpatients undergoing treatment with their own report on a side effects checklist. These were rated according to frequency and the degree of trouble they caused. Their data described a stunning difference:

The mean number of side effects reported by the patients on the TSES (Toronto Side Effects Scale) was 20 times higher than the number recorded by the psychiatrists.”

Their conclusion is disturbing:

Psychiatrists may not be aware of most side effects experienced by psychiatric outpatients receiving ongoing pharmacologic treatment for depression.”

Friends, consider the functional medicine approach that objectively evaluates the underlying causal physiology of depression and applies evidence-based interventions on an individual basis that are free of side effects.

Antidepressants associated with strokes in women

Here we have another good reason to use the body-friendly method of providing native precursors and cofactors to naturally increase neurotransmitters instead of using re-uptake inhibitors. This study just published in the Archives of Internal Medicine found that “Selective serotonin reuptake inhibitor (SSRI) use was associated with increased stroke risk and all-cause mortality…SSRI use was associated with incident hemorrhagic stroke and fatal stroke.” Important: there IS another way, without side effects or hazards, to improve neurotransmitter levels. Contact us for more information.

St John’s wort as effective for major depression as standard antidepressants

Functional medicine treatment of the underlying biological component of depression involves much more than modulating serotonin activity (and taking only St John’s Wort), but the results of this study are worth noting. After reviewing a total of 29 trials (5489 patients) that included 18 comparisons with placebo and 17 comparisons with synthetic standard antidepressants, the authors concluded: “The available evidence suggests that the hypericum extracts tested in the included trials a) are superior to placebo in patients with major depression; b) are similarly effective as standard antidepressants; c) and have fewer side effects than standard antidepressants.” [Note: hypericum = St John's Wort]