Inflammation reduces the brain’s response to rewards in women, but not in men, according to a new study in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging, published by Elsevier. Reduced activity in the brain’s reward center is the signature of anhedonia, a core feature of depression that reflects a loss of enjoyment in things or activities. Women are two-to-three times more likely to be diagnosed with depression, and the new findings pinpoint a key difference in men and women that could contribute to the lopsided rates of the disorder.
“Our study is the first to show that there are sex differences in neural sensitivity to reward in response to inflammation, which has important implications,” said senior author Naomi Eisenberger, PhD, University of California, Los Angeles.
“This may suggest one reason women experience depression at a far greater rate than men, particularly for the kinds of depression that may be inflammatory in nature.”
In the study, healthy men and women received a substance to increase inflammation. Dr. Eisenberger and colleagues measured activity in the reward region of the brain, the ventral striatum, while the participants played a game to receive a monetary reward. Women with greater inflammatory responses showed less brain response in anticipation of potential rewards, but the relationship was not present in men.
“This suggests that women with chronic inflammatory disorders may be particularly vulnerable to developing depression through decreases in sensitivity to reward. Clinicians who treat female patients with inflammatory disorders may want to pay close attention to these patients for possible onset of depressive symptoms,” said first author Mona Moieni, PhD, a postdoctoral researcher in the laboratory of Dr. Eisenberger.
“This study highlights the important gender differences that exist in the human brain and suggests a mechanism that might help explain the greater prevalence of depression in women compared to men,” said Cameron Carter, MD, Editor of Biological Psychiatry: Cognitive Neuroscience and Neuroimaging.
Because the increased inflammation had no effect on how men’s brains responded to reward, inflammation-induced anhedonia may be an important contributor to the increased rates of depression in women.
Rhiannon Bugno – Elsevier
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Original Research: Closed access
“Sex Differences in the Relationship Between Inflammation and Reward Sensitivity: A Randomized Controlled Trial of Endotoxin”.Naomi Eisenberger et al.
Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. doi:10.1016/j.bpsc.2019.03.010
Sex Differences in the Relationship Between Inflammation and Reward Sensitivity: A Randomized Controlled Trial of Endotoxin
There are robust sex differences in the prevalence of depression. Inflammation and anhedonia may play a role in understanding these sex differences. Indeed, sex differences in inflammation-induced neural responses to reward may provide insight into the sex gaps in depression, but no study has examined this question.
As such, the current study examined whether there were sex differences in reward-related neural activity (i.e., ventral striatum [VS] activity) in response to an experimental inflammatory challenge. Human participants (N = 115; 69 female) were randomly assigned to receive either placebo or low-dose endotoxin, which increases inflammation in a safe, time-limited manner. Two hours after receiving placebo or endotoxin (the height of the inflammatory response to endotoxin), participants completed a task in which they anticipated monetary reward in a functional magnetic resonance imaging scanner.
Results demonstrated that endotoxin (vs. placebo) led to reduced VS activity in anticipation of reward and that there were sex differences in this effect. Specifically, in female participants, endotoxin (vs. placebo) led to decreased VS activity in anticipation of reward, but this effect was not present in male participants. In addition, within the endotoxin condition, decreases in VS activity in anticipation of reward were related to increases in inflammation for female but not male participants.
These findings may have implications for understanding how inflammation may contribute to sex differences in rates of depression