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.

Whole-genome sequencing analysis of semi-supercentenarians

Massimo Delledonne
;
Alberto Ferrarini;Nicola Martinelli;Domenico Girelli;Oliviero Olivieri;
2021-01-01

Abstract

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.
2021
ageing
clonal hematopoiesis
genetics
genomics
geroscience
human
longevity
semi-supercentenarians
sequencing
Aged
Aged, 80 and over
Clonal Hematopoiesis
Cohort Studies
Female
Genetic Background
Humans
Italy
Longevity
Male
Middle Aged
Mutation
Whole Genome Sequencing
DNA Repair
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1057469
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