Thursday, April 3, 2025

Shingles Vaccine May Also Reduce Risk of Dementia, Study Shows

Making use of a Welsh vaccination policy that set strict and defined eligibility criteria for receiving the herpes zoster (shingles) vaccine, researchers have found that shingles vaccination may also significantly reduce the probability of dementia. The findings were published yesterday in Nature.

Previous research has found an association between the shingles vaccine and reduced dementia risk. However, those studies could not determine whether adults who chose to get vaccinated had other fundamental differences in lifestyle or motivation than adults who did not, noted Markus Eyting, Ph.D., of Stanford University, and colleagues.

In 2013, Wales instituted a policy whereby individuals born after September 2, 1933, were progressively eligible for a live-attenuated shingles vaccine; those born before that date were never eligible. Eyting and colleagues noted that this created a “natural experiment” in which they could avoid many confounding variables present in earlier studies.

Drawing on electronic health record registries, the researchers compiled data on 282,541 adults born between September 1, 1925, and September 1, 1942, who were dementia-free prior to the rollout of the vaccine program. These naturally occurring comparison groups did not differ appreciably from each other in ways that might affect the risk for dementia.

During a follow-up period of seven years, a little more than 14,000 adults in the study sample had at least one diagnosis of shingles, while around 35,000 were newly diagnosed with dementia. After adjusting for age differences, the researchers found that adults who were eligible for the shingles vaccine had an 18.8% lower risk of a shingles diagnosis than the ineligible adults, while adults who actually received the vaccine had a 37.2% lower risk of shingles. Similarly, adults eligible for the vaccine had an 8.5% reduced risk of a dementia diagnosis during the follow-up period, while those who took the vaccine had a 20% reduced risk. Differences were seen even between individuals born weeks before or after the eligibility date. This protective effect was stronger among women than men.

The researchers replicated these findings in a larger study that combined the populations of Wales and England—which had a similar vaccine rollout initiative—and used a different variable for assessing dementia (death certificates showing death with dementia as a primary cause).

“Our substantial effect sizes, combined with the relatively low cost of the zoster vaccine, imply that, if these findings are truly causal, the zoster vaccine will be both far more effective as well as cost-effective in preventing or delaying dementia than existing pharmaceutical interventions,” Eyting and colleagues concluded.

For related information, see the Psychiatric News article “Dementia Cases Projected to Double: Clinicians, Policymakers Can Help Reduce Risk.”

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Wednesday, April 2, 2025

Taking Hormonal Contraception Postpartum May Raise Risk of Depression

Starting most hormonal contraceptives in the first year postpartum may raise the risk of depression even among first-time mothers with no recent history of the disorder, according to a study published by JAMA Network Open.

“This study observed that the hormonal contraceptive initiation postpartum was associated with an increased risk of depression across all age groups,” wrote Soren Vinther Larsen, Ph.D., of Copenhagen University Hospital–Rigshospitalet, and colleagues. The risk was increased for all hormonal contraceptives except for progestogen-only “mini-pills,” for which risk was inconclusive.

Using Danish registry data, the researchers examined health records for 610,038 first-time mothers who gave birth between 1997 and 2022, of whom 41% started a hormonal contraceptive within 12 months of delivery. The researchers excluded women who had depression within 24 months before giving birth, multiple births, or stillbirth. Depression was defined as filling a prescription for an antidepressant or receiving a hospital discharge with a diagnosis of depression within 12 months of delivery.

Overall, there were 21 cases of depression per 1,000 person-years among women who started hormonal contraceptives, compared with 14 per 1,000 person-years among those who did not. This amounted to a 49% higher risk of depression among hormonal contraceptive users compared with nonusers, after adjusting for factors like age, history of mental illness, or birth complications. The absolute prevalence of postpartum depression was 1.54% among all women, which the researchers calculated would have been 1.36% had no one taken contraceptives.

The researchers observed this elevated risk of depression for several types of hormonal contraceptives: combined-hormone pills and combined nonoral (patch and vaginal ring) or progestogen-only nonoral (implants, depot injections, and levonorgestrel-releasing IUDs). Progestogen-only mini-pills were an exception, for which an increased risk was evident only after eight months postpartum.

The risk varied by type of hormonal contraceptive: Compared with nonuse, levonorgestrel-releasing IUDs raised risk of depression by 27% during the study period, progestogen-only nonoral contraceptives by 40%, combined-hormone pills by 72%, and combined-hormone patches and vaginal rings by 97%.

“These findings raise the issue of whether the incidence of depression postpartum may be inflated by routine hormonal contraceptive initiation, which is important information to convey at postpartum contraceptive counseling,” Larsen and colleagues wrote.

For related information, see the Psychiatric News article “Depression After Hormonal Contraception Initiation Linked to PPD.”

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Tuesday, April 1, 2025

Eating Disorders Affect More Racially Diverse Population Than Previously Thought

Eating disorders are often thought to primarily affect White people, but a study in the International Journal of Eating Disorders suggests that eating disorders affect college students at largely similar rates across racial and ethnic groups. Furthermore, where differences emerged along racial and ethnic lines, some minoritized groups had a greater probable prevalence and severity of eating disorders than Whites.

Carli P. Howe, a graduate student at the University of Washington in St. Louis, and colleagues analyzed data from 3,929 students from 26 U.S. colleges and universities whose results on a mental health screen suggested the presence of an eating disorder. Participants self-identified as Asian, Black, Hispanic, multiracial, or White. They were also asked about their gender identity and were categorized as men, women, cisgender, or non-cisgender.

The researchers found that:

  • Non-cisgender Asian participants had the highest prevalence of probable anorexia nervosa (8.64%), followed by cisgender Asian women (3.61%), non-cisgender multiracial participants (3.28%), and cisgender multiracial women (2.5%).
  • Non-cisgender Hispanic participants had the highest prevalence of probable clinical or subclinical bulimia nervosa/binge eating disorder (20.49%), followed by cisgender Hispanic women (18.2%), cisgender multiracial women (17.25%), and cisgender White women (15.54%).
  • Non-cisgender Black participants were most likely to be at high risk for eating disorder onset (6.67%), followed by cisgender Hispanic women (5.87%), cisgender White women (4.83%), and cisgender Black women (4.52%).
  • Among participants with probable eating disorders, there were no significant differences between racial or ethnic groups across any gender with respect to the frequency of eating disorder behaviors such as binge eating, vomiting, or laxative/diuretic use in the past three months.

“These findings are key for refuting widely held stereotypes that [eating disorders] primarily affect White individuals and also underscore a critical need for solutions aimed to equitably address [eating disorders] in college populations,” the researchers wrote.

They added that universal screening and intervention for eating disorders on college campuses have the potential to significantly reduce the population prevalence of eating disorders in college students: “Such universally delivered programs may include targeted interventions for racially/ethnically minoritized students. These directions represent a critical path to closing the large [eating disorder] treatment gap in this high-risk population.”

For further information, see the Psychiatric Services article “Eating Disorder Treatment Access in the United States: Perceived Inequities Among Treatment Seekers.”

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