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将所有因素联系起来:端粒、两性体型差异与预期寿命的性别差距。

Tying it all together: telomeres, sexual size dimorphism and the gender gap in life expectancy.

作者信息

Stindl Reinhard

机构信息

Institut für Medizinische Biologie, Medizinische Universität Wien, Währingerstrasse 10, 1090 Vienna, Austria.

出版信息

Med Hypotheses. 2004;62(1):151-4. doi: 10.1016/s0306-9877(03)00316-5.

Abstract

The classic explanation that women outlive men solely due to hormonal and lifestyle differences, does not withstand a critical analysis. In developed countries, the average gap in life expectancy between the sexes is 7 years. It has widened over the last decades, despite the trend of women copying the 'unhealthy' lifestyle of men. Estrogen levels in postmenopausal women are virtually identical to estrogen levels in males and can hardly explain the discrepancy. Furthermore, testosterone got its bad reputation from one study on mentally retarded men, which has to be interpreted with caution. However, sexual size dimorphism with men being the larger sex in conjunction with the limited replication potential of human somatic cells might account for higher mortality rates in males, especially at old age. The hypothesis, as presented here, is based on the well-known concept of a cellular mitotic clock, which was discovered by Leonard Hayflick almost half a century ago. The underlying counting mechanism, namely the gradual erosion of chromosome ends (telomeres) due to the end replication problem of linear DNA molecules, was first described by Alexey Olovnikov in 1971 and with minor modifications has become a widely accepted paradigm. In a recent Lancet study, an inverse correlation between mean telomere length and mortality in people has been found. In this and two other studies, it was confirmed that males do have shorter telomeres than females at the same age. This is almost certainly a consequence of men being usually taller than women, although nobody has done an investigation yet. Clearly, a larger body requires more cell doublings, especially due to the ongoing regeneration of tissues over a lifetime. Accordingly, the replicative history of male cells might be longer than that of female cells, resulting in the exhaustion of the regeneration potential and the early onset of age-associated diseases predominantly in large-bodied males. Inherited telomere length variation between unrelated individuals might have obscured a clear correlation between body height and mortality, leading to conflicting results in some studies. Finally, I propose that the secular height increase over the last decades, of about 2.5 cm per generation in the western world, has to be blamed for the widening of the gender gap in life expectancy.

摘要

认为女性比男性长寿完全是由于激素和生活方式差异的传统解释,经不起批判性分析。在发达国家,男女平均预期寿命差距为7岁。尽管有女性效仿男性“不健康”生活方式的趋势,但在过去几十年里,这一差距仍在扩大。绝经后女性的雌激素水平与男性几乎相同,几乎无法解释这种差异。此外,睾酮的坏名声源于一项针对智障男性的研究,对此必须谨慎解读。然而,男性体型较大的性二态性以及人类体细胞有限的复制潜力,可能导致男性死亡率较高,尤其是在老年时。本文提出的这一假说基于一个著名的细胞有丝分裂时钟概念,该概念是近半个世纪前由伦纳德·海弗利克发现的。潜在的计数机制,即由于线性DNA分子的末端复制问题导致染色体末端(端粒)逐渐磨损,最早由阿列克谢·奥洛夫尼科夫在1971年描述,经过微小修改后已成为广泛接受的范式。在最近一项发表于《柳叶刀》的研究中,发现了人群中端粒平均长度与死亡率之间存在负相关。在这项研究以及其他两项研究中,证实了在相同年龄下,男性的端粒确实比女性短。这几乎肯定是男性通常比女性高的结果,尽管目前还没有人对此进行过调查。显然,体型较大需要更多的细胞倍增,特别是由于一生中组织的持续再生。因此,男性细胞的复制历史可能比女性细胞更长,导致再生潜力耗尽,与年龄相关的疾病主要在体型较大的男性中更早出现。无关个体之间遗传的端粒长度差异可能掩盖了身高与死亡率之间的明显相关性,导致一些研究结果相互矛盾。最后,我认为过去几十年西方世界每代人身高约增加2.5厘米的长期增长趋势,应归咎于男女预期寿命差距的扩大。

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