Elevation of 11β-hydroxysteroid dehydrogenase type 2 activity in Holocaust survivor offspring: Evidence for an intergenerational effect of maternal trauma exposure

被引:43
作者
Bierer, Linda M. [1 ,2 ]
Bader, Heather N. [1 ,2 ]
Daskalakis, Nikolaos P. [1 ,2 ]
Lehrner, Amy L. [1 ,2 ]
Makotkine, Iouri [1 ,2 ]
Seckl, Jonathan R. [3 ]
Yehuda, Rachel [1 ,2 ]
机构
[1] James J Peters VA Med Ctr, Bronx, NY USA
[2] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA
[3] Univ Edinburgh, Queens Med Res Inst, Edinburgh EH16 4TJ, Midlothian, Scotland
关键词
11 beta-Hydroxysterioddehydrogenase type 2; Cortisol; Gtucocorticoid metabolism; Developmental programming; Intergenerational; Holocaust; Offspring; Biomarkers; PTSD; HPA axis; BETA-HYDROXYSTEROID DEHYDROGENASE; POSTTRAUMATIC-STRESS-DISORDER; MESSENGER-RIBONUCLEIC-ACID; GLUCOCORTICOID-RECEPTOR; PRENATAL STRESS; LOW CORTISOL; EPIGENETIC REGULATION; PARENTAL PTSD; EXPRESSION; MECHANISMS;
D O I
10.1016/j.psyneuen.2014.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Adult offspring of Holocaust survivors comprise an informative cohort in which to study intergenerational transmission of the effects of trauma exposure. Lower cortisol and enhanced glucocorticoid sensitivity have been previously demonstrated in Holocaust survivors with PTSD, and in offspring of Holocaust survivors in association with maternal PTSD. In other work, reduction in the activity of the enzyme 11 beta-hydroxysteroid dehydrogenase type 2 (11 beta-HSD-2), which inactivates cortisol, was identified in Holocaust survivors in comparison to age-matched, unexposed Jewish controls. Therefore, we investigated glucocorticoid metabolism in offspring of Holocaust survivors to evaluate if similar enzymatic decrements would be observed that might help to explain glucocorticoid alterations previously shown for Holocaust offspring. Methods: Holocaust offspring (n = 85) and comparison subjects (n = 27) were evaluated with clinical diagnostic interview and self-rating scales, and asked to collect a 24-h urine sample from which concentrations of cortisol and glucocorticoid metabolites were assayed by GCMS. 11 beta-HSD-2 activity was determined as the ratio of urinary cortisone to cortisol. Results: Significantly reduced cortisol excretion was observed in Holocaust offspring compared to controls (p = .046), as had been shown for Holocaust survivors. However, 11 beta-HSD-2 activity was elevated for offspring compared to controls (p = .008), particularly among those whose mothers had been children, rather than adolescents or adults, during World War II (p = .032). The effect of paternal Holocaust exposure could not be reliably investigated in the current sample. Conclusions: The inverse association of offspring 11 beta-HSD-2 activity with maternal age at Holocaust exposure is consistent with the influence of glucocorticoid programming. Whereas a tong standing reduction in 11 beta-HSD-2 activity among survivors is readily interpreted, in the context of Holocaust related deprivation, understanding the directional effect on offspring will require replication and further exploration. Published by Elsevier Ltd.
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页码:1 / 10
页数:10
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