Laron Zvi
Endocrinology and Diabetes Research Unit, Schneider Children's Medical Center of Israel, Petah Tikva, Sackler Faculty of Medicine, Tel Aviv University, Israel.
Hormones (Athens). 2008 Jan-Mar;7(1):24-7. doi: 10.14310/horm.2002.1111034.
Primary or secondary IGF1 deficiency has been implicated in shortening of lifespan. This paper reviews available data on the influence of IGF1 deficiency on lifespan and longevity in animals and man. It has been shown that inactivation of the IGF1 gene or of the GH receptor in both invertebrates (C-elegans, flies-Drosphila) and rodents (mice and rats), leading to IGF1 deficiency, prolong life, particularly in females. In man, evaluation of the 2 largest cohorts of patients with Laron syndrome (inactive GH receptor resulting in IGF1 deficiency) in Israel and Ecuador revealed that despite their dwarfism and marked obesity, patients are alive at the ages of 75-78 years, with some having reached even more advanced ages. It is assumed that a major contributing factor is their protection from cancer, a major cause of death in the general population.
原发性或继发性胰岛素样生长因子1(IGF1)缺乏与寿命缩短有关。本文综述了关于IGF1缺乏对动物和人类寿命及长寿影响的现有数据。研究表明,在无脊椎动物(秀丽隐杆线虫、果蝇)和啮齿动物(小鼠和大鼠)中,IGF1基因或生长激素受体的失活导致IGF1缺乏,可延长寿命,尤其是在雌性动物中。在人类中,对以色列和厄瓜多尔两个最大的拉龙综合征患者队列(生长激素受体无活性导致IGF1缺乏)的评估显示,尽管患者身材矮小且明显肥胖,但他们活到了75 - 78岁,有些甚至年龄更大。据推测,一个主要的促成因素是他们对癌症具有抵抗力,而癌症是普通人群的主要死因。