Department of Experimental, Diagnostic, and Specialty Medicine (DIMES), University of Bologna, Bologna, Italy.
Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institutet at Huddinge University Hospital, Stockholm, Sweden.
Elife. 2021 May 4;10:e57849. doi: 10.7554/eLife.57849.
Extreme longevity is the paradigm of healthy aging as individuals who reached the extreme decades of human life avoided or largely postponed all major age-related diseases. In this study, we sequenced at high coverage (90X) the whole genome of 81 semi-supercentenarians and supercentenarians [105+/110+] (mean age: 106.6 ± 1.6) and of 36 healthy unrelated geographically matched controls (mean age 68.0 ± 5.9) recruited in Italy. The results showed that 105+/110+ are characterized by a peculiar genetic background associated with efficient DNA repair mechanisms, as evidenced by both germline data (common and rare variants) and somatic mutations patterns (lower mutation load if compared to younger healthy controls). Results were replicated in a second independent cohort of 333 Italian centenarians and 358 geographically matched controls. The genetics of 105+/110+ identified DNA repair and clonal haematopoiesis as crucial players for healthy aging and for the protection from cardiovascular events.
超长寿命是健康衰老的典范,因为达到人类生命极限的个体避免或在很大程度上推迟了所有与年龄相关的主要疾病。在这项研究中,我们以高覆盖率(90X)对 81 名半超级百岁老人和超级百岁老人[105+/110+](平均年龄:106.6 ± 1.6)和 36 名健康的、无血缘关系的、地理位置匹配的对照组(平均年龄 68.0 ± 5.9)的全基因组进行了测序,这些人都在意大利招募。结果表明,105+/110+的特征是与有效的 DNA 修复机制相关的特殊遗传背景,这一点从种系数据(常见和罕见变体)和体细胞突变模式(与年轻的健康对照组相比,突变负荷较低)中都得到了证实。在意大利的第二个独立队列中,对 333 名百岁老人和 358 名地理位置匹配的对照组进行了复制。105+/110+的遗传学将 DNA 修复和克隆性造血作用确定为健康衰老和预防心血管事件的关键因素。