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1 STOCHASTIC MORTALITY MODELS: Criteria for Assessing and Comparing Models ANDREW CAIRNS Heriot-Watt University, Edinburgh and The Maxwell Institute, Edinburgh Joint work with David Blake & Kevin Dowd and JP Morgan LifeMetrics team

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Page 1: 1 STOCHASTIC MORTALITY MODELS › ~andrewc › ohp › cairns_paris2008.pdf · 1 STOCHASTIC MORTALITY MODELS: Criteria for Assessing and Comparing Models ANDREW CAIRNS Heriot-Watt

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STOCHASTIC MORTALITY MODELS:

Criteria for Assessing and Comparing Models

ANDREW CAIRNS

Heriot-Watt University, Edinburgh

and The Maxwell Institute, Edinburgh

Joint work with David Blake & Kevin Dowd

and JP Morgan LifeMetrics team

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PLAN FOR TALK

• Background remarks

• Two families of models

• Criteria for evaluating different models

– quantitative

– qualitative

• Closing remarks

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The Problem

2007: What we know as the facts:

• Life expectancy is increasing.

• Future development of life expectancy is uncertain.

“Longevity risk”

⇒ Systematic risk for pension plans and annuity

providers

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The Problem – UK Defined-Benefit Pension Plans:

• Before 2000:

– High equity returns masked impact of longevity

improvements

• After 2000:

– Poor equity returns, low interest rates

– Decades of longevity improvements now a problem

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Why do we need stochastic mortality models?

Data⇒ future mortality is uncertain

• Good risk management

• Setting risk reserves

• Life insurance contracts with embedded options

• Pricing and hedging mortality-linked securities

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Stochastic mortality

• Many models to choose from

• Limited data⇒ model and parameter risk

(*) Cairns et al. (2007) A quantitative comparison of stochastic mortality models.... Online: www.lifemetrics.com

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Measures of mortality

• q(t, x) = underlying mortality rate in year t at age x

•m(t, x) = underlying death rate

• Assume q(t, x) = 1− exp[−m(t, x)]

Poisson model:

Actual deaths D(t, x) ∼ Poisson (m(t, x)E(t, x))

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Two general families of models

log m(t, x) = β(1)x κ

(1)t γ

(1)t−x + . . . + β(N)

x κ(N)t γ

(N)t−x

OR

logitq(t, x) = β(1)x κ

(1)t γ

(1)t−x + . . . + β(N)

x κ(N)t γ

(N)t−x

• β(k)x = age effect for component k

• κ(k)t = period effect for component k

• γ(k)t−x = cohort effect for component k

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e.g. Lee-Carter (1992) model

log m(t, x) = β(1)x + β(2)

x κ(2)t =

2∑i=1

β(i)x κ

(i)t γ

(i)t−x

• N = 2 components

• β(1)x , β

(2)x age effects

• κ(2)t single random period effect

• κ(1)t ≡ 1

• γ(1)t−x = γ

(2)t−x ≡ 1 (model has no cohort effect)

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Six Models

Lee-Carter (1992) LC

log m(t, x) = β(1)x + β

(2)x κ

(2)t

Renshaw-Haberman (2006) RH

log m(t, x) = β(1)x + β

(2)x κ

(2)t +β

(3)x γ

(3)t−x

Age-Period-Cohort APC

log m(t, x) = β(1)x + 1×κ

(2)t + 1×γ

(3)t−x

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Cairns-Blake-Dowd (2006) CBD-1

logitq(t, x) = κ(1)t + (x− x̄)κ

(2)t

Cairns et al. (2007) CBD-2

logitq(t, x) =

κ(1)t + (x− x̄)κ

(2)t +

((x− x̄)2 − σ2

x

(3)t + γ

(4)t−x

Cairns et al. (2007) CBD-3

logitq(t, x) = κ(1)t + (x− x̄)κ

(2)t + (xc − x)γ

(3)t−x

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How to compare stochastic models (*)

• Quantitative criteria

• Qualitative criteria

– parsimony and transparency

– robust relative to age and period range

– biologically reasonable

– forecasts are reasonable

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Quantitative Criteria

Bayes Information Criterion (BIC)

• Model k: l̂k = model maximum likelihood

• BIC penalises over-parametrised models

• BICk = l̂k − 12nk log N

– nk = number of parameters

– N = number of observations

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Quantitative Criteria – BIC

England & Wales males, 1961-2004, ages 60-89

Model Max log-lik. # parameters BIC (rank)

LC -8912.7 102 -9275.8 (5)

RH -7735.6 203 -8458.1 (3)

APC -8608.1 144 -9120.6 (4)

CBD-1 -10035.5 88 -10348.8 (6)

CBD-2 -7702.1 202 -8421.1 (2)

CBD-3 -7823.7 161 -8396.8 (1)

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The BIC doesn’t tell us the whole story ...

Qualitative Criteria – Graphical diagnostics

• Poisson model⇒ (t, x) cells are all independent.

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Are standardised residuals i.i.d.?

1970 1980 1990 2000

6065

7075

8085

90

CBD−1 model

Year

Age

1970 1980 1990 2000

6065

7075

8085

90

CBD−2 model

Year

Age

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Mortality Fan Charts + A plausible set of forecasts

1960 1980 2000 2020 2040

0.00

50.

010

0.02

00.

050

0.10

00.

200

AGE 65

AGE 75

AGE 85

Year, t

Mor

talit

y ra

te, q

(t,x

)

Model CBD−1 Fan Chart

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Model risk

1960 1980 2000 2020 2040

0.00

50.

010

0.02

00.

050

0.10

00.

200

AGE 65

AGE 75

AGE 85

Year, t

Mor

talit

y ra

te, q

(t,x

)

Model CBD−1 Fan Chart

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Model risk

1960 1980 2000 2020 2040

0.00

50.

010

0.02

00.

050

0.10

00.

200

AGE 65

AGE 75

AGE 85

Year, t

Mor

talit

y ra

te, q

(t,x

)

Combined CBD−1, CBD−2 Fan Chart

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Model risk

1960 1980 2000 2020 2040

0.00

50.

010

0.02

00.

050

0.10

00.

200

AGE 65

AGE 75

AGE 85

Year, t

Mor

talit

y ra

te, q

(t,x

)

Combined CBD−1, CBD−2, CBD−3 Fan Chart

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Robustness: e.g. Age-Period-Cohort model

1960 1980 2000 2020 2040

0.01

0.02

0.05

0.10

1961−2004 data: APC full1961−2004 data: APC limited1981−2004 data: APC

APC Model − Age 75 Mortality Rates

Year, t

Mor

talit

y ra

te

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Not all models are robust: Renshaw-Haberman model

1960 1980 2000 2020 2040

0.00

50.

020

0.05

00.

200

1961−2004 data: R−H full1961−2004 data: R−H limited1981−2004 data: R−H

Model R−H (ARIMA(1,1,0)) projections

Year, t

Coh

ort e

ffect

x=65

x=75

x=85

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Robustness Problem

• Likely reason: Likelihood function has multiple maxima

• Consequences:

– Lack of robustness within sample

– Lack of robustness in forecasts

∗ central trajectory

∗ prediction intervals

– Some sample periods⇒ implausible forecasts

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Concluding remarks

• Range of models to choose from

• Quantitative criteria is only the starting point

• Additional criteria⇒– Some models pass

– Some models fail

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References

• Cairns, A.J.G., Blake, D., Dowd, K., Coughlan, G.D., Epstein, D., Ong, A., and Belevich, I.

(2007) A quantitative comparison of stochastic mortality models using data from England and

Wales and the United States. Preprint.

• Cairns, A.J.G., Blake, D., Dowd, K., Coughlan, G., Epstein, D., and Khallaf-Allah M. (2008) The

Plausibility of Mortality Density Forecasts: An Analysis of Six Stochastic Mortality Models.

Preprint - forthcoming.