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Prospects for extending healthy life a lot

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Title: Prospects for extending healthy life a lot


1
Prospects for extending healthy life - a
lot Aubrey D.N.J. de Grey Chairman and CSO,
Methuselah Foundation Lorton, VA, USA and
Cambridge, UK Email aubrey_at_sens.org MF website
http//www.methuselahfoundation.org/ Science
website http//www.sens.org/
2
  • Shameless plug 1
  • The SENS conferences a unique synthesis of
    research on technologies to repair the molecular
    and cellular damage of aging
  • SENS 3 - Cambridge UK, Sept. 6-10 2007
  • http//www.sens.org/sens3/

3
Shameless plug 2
Out Sept 4
4
  • Structure of this talk
  • Longevity escape velocity why 30 years is
    probably equivalent to eternity
  • - The SENS plan, with detail on one element
  • Methuselah Foundation activities and plans

5
  • Structure of this talk
  • Longevity escape velocity why 30 years is
    probably equivalent to eternity
  • - The SENS plan, with detail on one element
  • Methuselah Foundation activities and plans

6
A statement without which my life would be a lot
simpler The first 1000-year-old is
probably less than 20 years younger
than the first 150-year-old
7
Aging in a nutshell Product of evolutionary
nelect, not intent Metabolism ongoingly causes
damage Damage eventually causes
pathology Pathology causes more pathology
8
Strategies for intervention Gerontology
Geriatrics Metabolism
Damage Pathology
9
Strategies for intervention Gerontology
Engineering Geriatrics Metabolism
Damage Pathology Claim
unlike the others, the engineering approach may
achieve a large extension of human healthy
lifespan quite soon
10
How to make a car last 50 years -- plan A
11
How to make a car last 50 years -- plan B
12
  • Reasons for the engineering approach
  • it targets initially inert intermediates
    (damage)
  • repairing damage buys time

13
Retarding aging benefits modest
max
Reserve
frail
0
0
Age
Halving rate of damage starting in middle age -
doubles remaining healthspan - raises total
healthspan by maybe 20
14
Comparable repair far better
max
hard
Reserve
easy
frail
0
0
Age
Fixing half the damage starting in middle age -
doubles total healthspan - raises remaining
healthspan maybe 5-fold
15
Ever-improving repair better yet
max
very hard
Reserve
hard
easy
frail
0
0
Age
Fixing half the damage, then 3/4 - not as good
as doing 3/4 first time - but better than doing
1/2 first time
16
Infinitely better, in fact
max
Reserve
frail
0
0
Age
Fixing half the damage, then 3/4, then 7/8. -
outpaces the so-far-unfixable damage -
maintains healthspan indefinitely
17
Robust human rejuvenation (RHR) Addition of 30
extra years of healthy life (and total life) to
people who are already in middle age when
treatment is begun
18
Longevity escape velocity (LEV) The rate at
which rejuvenation therapies must improve
(following achievement of RHR) in order to
outpace the accumulation of
so-far-irreparable damage
19
Simulating aging (Phoenix de Grey, AGE, in
press) Metabolism ongoingly causes
damage and Damage eventually causes
pathology So. Simulations of aging (and
intervention) should simulate damage accumulation
20
  • Simulating damage basis
  • damage of many types accumulates
  • any can kill us (i.e. they are not additive)
  • within each type, subtypes are additive
  • damage feeds back to hasten more damage
  • people differ in damage accumulation rates
  • death is from damage X challenge (e.g. flu)

21
Simulating damage model Structural
parameters N_CAT The number of damage categories
each person has N_MECH The number of mechanisms
in each category MECH_WEIGHTm The contribution
of a mechanism to a category Fitting
parameters BASAL_M The mean basal damage
rate BASAL_SD The standard deviation of the
basal damage rate BASAL_H The homogeneity of
basal damage rate in a single person EXP_M The
mean exponential damage rate EXP_SD The standard
deviation of the exponential damage rate EXP_H
The homogeneity of exponential damage rate in a
single person FATAL_M The mean yearly
challenge FATAL_SD The standard deviation of the
yearly challenge Values set for each person at
initialisation PB Basal rate for the person
lognorm(BASAL_M, BASAL_SD) PE Exponential rate
for the person lognorm(EXP_M, EXP_SD) MBc,mBasal
rate for each mechanism lognorm(BASAL_M,
BASAL_SD)(1-BASAL_H) PBBASAL_H MEc,m
Exponential rate for each mechanism
lognorm(EXP_M, EXP_SD)(1-EXP_H) PEEXP_H
D_Mc,m Cumulative damage for each mechanism
0 D_Cc Cumulative damage for each category
0 Variables updated for each person at each time
step (year) Total damage PD(t) SUM
c1..N_CAT D_Cc(t) Damage increment
DI_Mc,m(t) MBc,m MEc,mPD(t-1) Cumulative
damage D_Mc,m(t) DI_Mc,m(t)
D_Mc,m(t-1) Cumulative category damage D_Cc(t)
SUM m1..N_MECH DI_Mc,m(t) Fatality
challenge FATAL(t) norm(FATAL_M,
FATAL_SD) If D_Cc(t) gt FATAL(t) for any c, the
person dies at age t
22
Validation age at death
23
Results how damage evolves
24
Results LEV in practice Therapies doubling in
efficacy every 42 y
0 50 100 150
200 250 300 350
25
Is this rate of progress plausible? Data
1903 1927
1949 1969
26
LEV decreases with time
max
Reserve
frail
0
0
Age
Fixing half the damage, then 2/3, then 3/4. -
still good enough - just like gravitational
escape velocity
27
Data
28
  • Structure of this talk
  • Longevity escape velocity why 30 years is
    probably equivalent to eternity
  • - The SENS plan, with detail on one element
  • Methuselah Foundation activities and plans

29
  • Reasons for the engineering approach
  • it targets initially inert intermediates
    (damage)
  • repairing damage buys time
  • damage is simpler than metabolism or pathology

30
Problem 1 this is metabolism
31
Problem 2this is the pathology
  • Alzheimers
  • Stroke
  • Sarcopenia
  • Osteoarthritis
  • Hormonal Imbalance
  • Kidney Failure
  • Cancer
  • Heart Disease
  • Diabetes
  • Incontinence
  • Osteoporosis
  • Macular Degeneration
  • Parkinsons
  • Pneumonia
  • Emphysema
  • Sex Drive
  • and LOTS more

32
This is the damage
Seven Deadly Things
  • Junk - Inside Cells
  • Junk - Outside Cells
  • Cells - Too Few
  • Cells - Too Many
  • Mutations - Chromosomes
  • Mutations - Mitochondria
  • Protein Crosslinks

No new type of damage identified since 1982!
33
Giving the middle-aged 30 years of
extra healthy life Robust Human
Rejuvenation
34
Giving the middle-aged 30 years of
extra healthy life Robust Human
Rejuvenation
35
Aggregates major examples - Proteins in
neurodegeneration - Oxysterols in atherosclerosis
36
Autophagy in Alzheimers Disease
Dystrophic Neurites
IEM
Calnexin
Cat D
37
Endothelial Cells
Lipid-engorged Lysosome
Foam Cell
38
  • Bioremediation the concept
  • - Microbes, like all life, need an ecological
    niche
  • - Some get it by brawn (growing very fast)
  • - Some by brain (living off material than others
    can't)
  • Any abundant, energy-rich organic material that
    is hard to degrade thus provides selective
    pressure to evolve the machinery to degrade it
  • - That selective pressure works. Even TNT, PCBs

39
Example DGGE Results from Perchlorate-Reducing,
Membrane Biofilm Reactors
40
Xenocatabolism the concept Graveyards -
are abundant in human remains - accumulate
bones (which are not energy-rich) - do not
accumulate oxysterols, tau etc... - so,
should harbour microbes that degrade them -
whose catabolic enzymes could be therapeutic
41
Environmental decontamination in vivo
42
7-ketocholesterol degradation - a good start
43
7-KC degradation - presented at meetings
44
First MF-funded paper submitted
45
  • Steps to biomedical application
  • Isolate competent strains select by starvation
  • Identify the enzymes (mutagenesis, chemistry,
    genomics)
  • Make lysosome-targeted transgenes, assay cell
    toxicity
  • Assay competence in vitro (more
    mutagenesis/selection)
  • Construct transgenic mice, assay toxicity in vivo
  • Assay competence in disease mouse models
  • Test in humans as for lysosomal storage diseases

46
  • Structure of this talk
  • Longevity escape velocity why 30 years is
    probably equivalent to eternity
  • - The SENS plan, with detail on one element
  • Methuselah Foundation activities, plans

47
  • The Methuselah Foundation current activities
  • Since 2002 Mprize in case SENS is not the
    best approach
  • Since 2004 Rejuvenation Research the
    top- ranked biogerontology journal
  • Since 2006 Funding of extramural SENS research

48
  • Planned organisational structure
  • Medium-term goal proof of concept in mice
  • Strategy solve/combine subgoals (SENS)
  • Procedure
  • implement subgoals 350 people
  • scientifically interesting and respected
  • best done extramurally by academics
  • combine in same mice 150 people
  • scientifically tedious and unrewarded
  • best done in-house by paid technicians

49
  • Funds current status
  • 4.5M in Mprize pot
  • Research pot being spent as fast as we fill it
  • LysoSENS being funded (100k/yr) by 2005-2006
    donations to the MF
  • MitoSENS being funded (150k/yr) by Peter
    Thiels donation of 500k
  • Thiels challenge pledge (3M) is 12 our next
    goal is to match it in full (i.e. raise 6M)

50
  • Ramping up.
  • Level 1 funding of 30k-300k per year
    guaranteed for at least 3 years. (This is where
    we are now.) Selected SENS strands supported at
    entry level (1 project/strand, 1-2 FTEs/project)
  • Level 2 funding of 300k-3m per year, three
    years. (This is where we will be when the Thiel
    pledge is fully matched.) Six SENS strands
    supported at minimal level (1-3 projects/strand,
    1-3 FTE/project)

51
  • Ramping up.
  • Level 3 funding of 3M-20M per year guaranteed
    for at least five years. Grant applications
    solicited 30-100 FTEs funded, across up to 30
    projects
  • Level 4 funding of 20M-100M per year, ten
    years. Physical facility (IBG) set up (50-150
    FTEs) extramural research support as in Level 3
    (100-350 FTEs)

52
  • Conclusions
  • - Reasonably thorough repair and obviation of
    ongoing molecular and cellular damage is
    foreseeable maybe 25-30 years away
  • - It will give a few decades extra life, but will
    buy time to give more, etc.
  • - 100,000 people die of aging every day our
    action today can thus save quite a few lives

53
Why I am doing this
54
Why I am doing this
55
Fun Not fun
Why I am doing this
56
  • Why I am doing this
  • I offer no apology for using media interest in
    life extension to make the biology of ageing an
    exception to Plancks observation that science
    advances funeral by funeral lives, lots of them,
    are at stake.
  • de Grey 2005, EMBO Reports 6(11)1000

57
Shameless plugs
SENS 3 - Cambridge UK, Sept. 6-10
2007 sens.org/sens3/ Ending Aging out 9/4
already available for pre-order at amazon.com
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