Herpes zoster and long-term risk of subjective cognitive decline

被引:1
作者
Yeh, Tian-Shin [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Curhan, Gary C. [4 ,5 ,8 ]
Yawn, Barbara P. [9 ]
Willett, Walter C. [3 ]
Curhan, Sharon G. [4 ,5 ]
机构
[1] Taipei Med Univ, Coll Med, Sch Med, Dept Phys Med & Rehabil, 250 Wuxing St, Taipei 11031, Taiwan
[2] Taipei Med Univ, Wan Fang Hosp, Dept Phys Med & Rehabil, Taipei, Taiwan
[3] Harvard Univ, Harvard TH Chan Sch Publ Hlth, Dept Epidemiol & Nutr, Boston, MA 02118 USA
[4] Brigham & Womens Hosp, Channing Div Network Med, Dept Med, Boston, MA 02115 USA
[5] Harvard Med Sch, Boston, MA 02115 USA
[6] Natl Taiwan Univ Hosp, Dept Phys Med & Rehabil, Taipei, Taiwan
[7] Natl Taiwan Univ, Coll Med, Dept Phys Med & Rehabil, Taipei, Taiwan
[8] Brigham & Womens Hosp, Dept Med, Renal Div, Boston, MA USA
[9] Univ Minnesota, Dept Family & Community Hlth, Minneapolis, MN USA
基金
美国国家卫生研究院;
关键词
Herpes zoster; Shingles; Subjective cognitive decline; Vaccination; Immunocompromise; APOE epsilon 4; Prospective cohort study; ALZHEIMERS-DISEASE; APOLIPOPROTEIN-E; CARDIOVASCULAR-DISEASE; MEMORY COMPLAINTS; NATIONAL-HEALTH; APOE EPSILON-4; SIMPLEX-VIRUS; US MEN; DEMENTIA; STROKE;
D O I
10.1186/s13195-024-01511-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundHerpes zoster (HZ), commonly known as "shingles," may contribute to cognitive decline through mechanisms such as neuroinflammation or direct neuronal injury. However, evidence on the longitudinal association between HZ and cognitive decline is conflicting and whether the risk differs by APOE epsilon 4-carrier status has not been studied; prospective cohort studies on the association between HZ vaccination and cognitive decline are also lacking.MethodsWe included 149,327 participants from three large cohorts-the Nurses' Health Study (NHS), NHSII, and Health Professionals Follow-Up Study (HPFS)-to prospectively examine the association between HZ and subsequent subjective cognitive decline (SCD). Poisson regression was used to estimate the multivariable-adjusted relative risk (MVRR) of a 3-unit increment in SCD score according to years since HZ compared with participants with no history of HZ.ResultsCompared with individuals with no history of HZ, the MVRR (95% CI) of a 3-unit increment in SCD score was significantly and independently higher among individuals with a history of HZ, but the duration of time since HZ when the elevated risk of SCD was statistically significant differed among the cohorts. In NHS, HZ was associated with higher long-term risk of SCD; compared with individuals with no history of HZ, the MVRR (95% CI) of a 3-unit increment in SCD score was 1.14 (1.01, 1.32) for >= 13 years since HZ. In NHS II, HZ was associated with higher risk of SCD in both the short-term [MVRR 1.34 (1.18, 1.53) for 1-4 years] and long-term [MVRR 1.20 (1.08, 1.34) for >= 13 years since HZ]. In HPFS, an elevated risk of SCD was suggested across all time points. Among the subset of participants with information on APOE epsilon 4, there was a suggestion that the association differed by APOE epsilon 4 carrier status, but the results were not consistent between women and men. Among the subset of women with information on HZ vaccination, there was a suggestion that the long-term risk of SCD may be greater among women who were not vaccinated against HZ.ConclusionsData from three large independent cohorts of women and men showed that HZ was associated with higher long-term risk of SCD, and the risk may differ by APOE epsilon 4-carrier status.
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页数:12
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