modelling changes in hiv prevalence among women attending antenatal clinics in uganda brian williams

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Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

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Page 1: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Modelling changes in HIV prevalence among women attending antenatal

clinics in Uganda

Brian Williams

Page 2: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

5

10

15

20

1970 1990 2010 2030

Pre

vale

nce

(%)

ANC women

Behaviour change in Uganda

Page 3: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

= birth rate

N = S + I

= rate at which new infections occur

= mortality

S I

I N SI /N I

S

The basic model

Page 4: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

20

40

60

80

100

1970 1990 2010 2030

Pre

vale

nce

(%)

012345678910

Inci

denc

e/M

orta

lity

(%/y

r)

ANC women in Uganda

R0 = 3.3

0

0

-1=70%

R

R

Page 5: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

= birth rate

N = S + I

= infection rate

I = Weibull mortality

S I

I N SI /N I

S

0.0

0.2

0.4

0.6

0.8

1.0

0 10 20 30Time (years)

P(s

urv

ivin

g)

Normal (Weibull 2)

Exponential(Weibull 1)

Page 6: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

20

40

60

80

1970 1990 2010 2030

Pre

vale

nce

(%)

0

2

4

6

8

10

12

Inci

denc

e/M

orta

lity

(%/y

r)

ANC women in Uganda

Page 7: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

= birth rate

N = population = e–P

I = Weibull mort.

~

~

S I

I N S I /N I S

0.0

0.2

0.4

0.6

0.8

1.0

0 10 20 30Prevalence (%)

Re

lativ

e t

ran

smis

sio

n

.

–Pe

Heterogeneity in sexual behaviour

Page 8: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

5

10

15

1970 1990 2010 2030

Pre

vale

nce

(%)

0

1

2

Inci

denc

e/M

orta

lity

(%/y

r)

ANC women in Uganda

Page 9: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0.0

0.2

0.4

0.6

0.8

1.0

1985 1990 1995 2000Year

Re

lativ

e t

ran

smis

sio

n

.

~

S I

I N SI /N I

S ~

= birth rate

N = population = C(t)

I = mortality

~

~

C(t)

Including control

Page 10: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

5

10

15

1970 1990 2010 2030

Pre

vale

nce

(%)

0

1

2

Inci

denc

e/M

orta

lity

(%/y

r)

ANC women in Uganda

Page 11: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

~

S I

I N SI /N I

S *

= birth rate

N = population = e

I = mortality

~

* –M

0.0

0.2

0.4

0.6

0.8

1.0

0 2 4Annual mortality (%)

Re

lativ

e t

ran

smis

sio

n

. –Me

Mortality leads to behaviour change

Page 12: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

0

5

10

15

1970 1990 2010 2030

Pre

vale

nce

(%)

0

1

2

Inci

denc

e/M

orta

lity

(%/y

r)

ANC women in Uganda

Page 13: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Nairobi

6 yr

Nunn P et al. Tuberculosis control in the era of HIV. Nat Rev Immunol. 2005 Oct;5(10):819-26.

Page 14: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

9.4

1.11.11.0

5.9

2.2

0

2

4

6

8

10

1991-1994 1995-1997 1998-1999

Ann

ual in

ciden

ce (

%)

.HI V- HI V+

TB incidence among gold miners in SACorbett EL Stable incidence rates of tuberculosis (TB) among human immunodeficiency virus (HIV)-negative South African gold miners during a decade of epidemic HIV-associated TB. J Infect Dis. 2003;188: 1156-63.

Page 15: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

SS+ Tuberculosis

Prevalence Incidence Disease Duration

(%) (%/yr) (yr)

HIV+ 0.44 (0.02-1.05) 2.87 (1.94-4.25) 0.15 (0.05-0.48)

HIV- 0.55 (0.14–0.95) 0.48 (0.27-0.84) 1.15 (0.48-1.13) DDR = 0.13 (0.09–0.20)

Gold miners in South Africa

We define disease duration as prevalence divided by incidence

Page 16: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Repeat the model 4 times, once for each stage of HIV. Use time series of HIV prevalence to determine incidence. Incidence gives rate at which people enter first stage; overall (Weibull) survival determines rate at which people move to next stage.

TB-HIV model

Williams BG et al. The impact of HIV/AIDS on the control of tuberculosis in India. PNAS 2005 102: 9619-9624.

Page 17: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Impact of interventions on TB cases in KenyaT

B in

cide

nce/

100k

/yr

800

600

400

200

0

.Baseline

ARV 80%

TLTI (6 m)

TLTI (life)

ARV 100%

TB detect.

TB cure

HIV incid

Base line:CDR = 50%CR = 70%Interventions:1% increase

1980 2000 2020 2040 Year

Currie, C. et al. Cost, affordability and cost-effectiveness of strategies to control tuberculosis in countries with high HIV prevalence. BMC, 2005. 5: 130.

Page 18: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Per

cent

Per

cent

HIV

pos

itive

HIV

neg

ativ

e

Williams BG et al. HIV Infection, Antiretroviral Therapy, and CD4+ Cell Count Distributions in African Populations. J Infect Dis, 2006 194: 1450-8.

Page 19: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

1,000

2,000

10 20

Time to death (yrs)

Initi

al C

D4/

L

Time to death (yrs)

1,000

2,000

10 20

Initi

al C

D4/

L

Model 1

CD4 decline independent of starting value

Survival determined by pre-infection CD4

Model 2

Survival independent of starting value

CD4 decline determine entirely by starting value and survival distribution

Page 20: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Spatial Epidemiology of HIV

Doubling time = 1 yearLife expectancy = 10 yearsNumber of partners = 4

Proportion of random partners chosen at random = 0 (left hand set) or 10% (right hand set) in the following slides.

Note that in this model migrants have exactly the same sexual behaviour and individual risk as non-migrants.

Page 21: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 22: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 23: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 24: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 25: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 26: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams
Page 27: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

1. Can we combine spatial/network models with our more conventional continuous time models of HIV?

2. Can we get a better understanding of the host-viral interaction?

3. What are the population level implications of 2?

4. Do we have enough data to explore fully the joint dynamics of TB and HIV?

Questions for all of us

Page 28: Modelling changes in HIV prevalence among women attending antenatal clinics in Uganda Brian Williams

Advice to young epidemiologists

Never make a calculation until you know the answer. Make an estimate before every calculation,

try a simple biological argument (R0, generation time, selection, survival, control). Guess the answer to every puzzle. Courage: no one else needs to know what the guess is. Therefore, make it quickly, by instinct. A right guess reinforces this instinct. A wrong guess brings the refreshment of surprise. In either case, life as an epidemiologist, however long, is more fun.

Plagiarised from E.F. Taylor and J.A. Wheeler Space-time Physics 1963