评估中世纪爱尔兰性别对死亡风险的影响

IF 1.7 2区 生物学 Q1 ANTHROPOLOGY
Allison C. Ham
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引用次数: 0

摘要

目的本研究评估性别对中世纪爱尔兰死亡风险的影响,以促进我们对过去对女性健康和生存有害的社会、生物和环境因素的理解。材料和方法从爱尔兰10个考古遗址中收集了335具骷髅的死亡年龄和性别数据,这些考古遗址可追溯到中世纪早期(公元500-1150年)和中世纪晚期(公元1150-1550年)时期。使用过渡分析(TA2)来估计所有骨盆和长骨骨骺明显融合的个体的死亡年龄。对于所有其他个体,使用牙齿发育和骨骺融合来估计死亡年龄。骨盆和头盖骨的形态特征和度量测量被用来估计性别。采用具有比例风险说明的Gompertz-Makeham风险模型来检验性别协变量对死亡风险的影响。结果在这种情况下,Gompertz-Makeham风险模型未能揭示性别对死亡风险的影响。性别对模型的影响在不同地点没有显著的时间变化。结论使用危害分析的结果未发现性别协变量对死亡率的影响。然而,在中世纪爱尔兰男性和女性之间观察到的相似的死亡率概况可能反映了文化障碍和/或不同的环境暴露,抵消了今天观察到的女性天生的生存优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluating the Effect of Sex on Mortality Risks in Medieval Ireland

Evaluating the Effect of Sex on Mortality Risks in Medieval Ireland

Objectives

This study evaluates the effect of sex on mortality risks in medieval Ireland to advance our understanding of the social, biological, and environmental factors that were deleterious to female health and survival in the past.

Materials and Methods

Data on age-at-death and sex was collected on 335 skeletonized individuals from 10 archaeological sites dating to the early medieval (500–1150 ce) and late medieval (1150–1550 ce) periods in Ireland. Transition analysis (TA2) was used to estimate age-at-death for all individuals with visibly fused pelvic and long bone epiphyses. For all other individuals, age-at-death was estimated using dental development and epiphyseal fusion. Morphological traits of the pelvis and cranium and metric measurements were used to estimate sex. A Gompertz-Makeham hazards model with a proportional hazards specification was used to examine the effect of the sex covariate on mortality risks.

Results

The Gompertz-Makeham hazards model failed to reveal an effect of sex on mortality risks in this context. No significant temporal variation in the effect of sex on the model was observed across sites.

Conclusions

The results failed to find an effect of the sex covariate on the mortality profile using hazards analysis. However, the similar mortality profiles observed between medieval Irish males and females could reflect cultural barriers and/or differential environmental exposures that counteracted the innate female survival advantage observed today.

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