Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

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Introduction to Introduction to Biostatistics II Biostatistics II Jane L. Meza, Jane L. Meza, Ph.D. Ph.D. October 24, 2005 October 24, 2005
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Transcript of Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Page 1: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Introduction to Introduction to Biostatistics IIBiostatistics II

Jane L. Meza, Ph.D.Jane L. Meza, Ph.D.

October 24, 2005October 24, 2005

Page 2: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Outline Hypothesis testing

Comparing 2 groups Paired t-test 2 Independent Samples t-test Wilcoxon Signed Ranks test Wilcoxon Rank Sum test

Comparing 3 or more groups ANOVA

One-Way Bonferroni Comparisons Repeated Measures Kruskal-Wallis

Chi-square

Regression Linear Correlation Linear Regression

Page 3: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Deck of Cards

If you randomly select a card, what is the probability the card is red?

If we draw 10 cards, how many of the 10 cards do we expect to be red?

Are we guaranteed that 5 of the cards will be red?

Page 4: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Deck of Cards Experiment Suppose we draw 10 cards

from a deck of 52 cards, and all 10 cards are red.

Is it possible that we could draw 10 red cards from a standard deck of cards?

Is it very likely that we could draw 10 red cards from a standard deck of cards?

We have conflicting information – we assumed that 50% of the cards were red, but in our sample 100% of the cards were red. What should we conclude?

Page 5: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Experiment

Why did you make that conclusion?

What assumptions are you making?

Is there a possibility that your conclusion is incorrect?

Page 6: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing

Start with an assumption (Null Hypothesis) 50% of the cards are red

Gather data Draw 10 cards

Page 7: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing Find the probability of the

results under your assumptions Find the probability of drawing 10

red cards, assuming that 50% of the 52 cards are red.

Probability of drawing 10 cards in a row is highly unlikely if 50% of the 52 cards are red (<0.001).

Page 8: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing

State your conclusion. Either we experienced a rare event,

or one of our assumptions is incorrect.

Since the probability of drawing 10 red cards is small, we conclude that our assumptions are probably incorrect.

We conclude that more than 50% of the cards are red.

Page 9: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing Example:Is There a Difference? Compare treatments or groups Psoriasis Example:

Some studies have suggested that psoriasis is more common among heavy alcohol drinkers.

Case-control study of men age 19-50. Cases were men who had psoriasis. Controls were men who did not have

psoriasis. All subjects completed questionnaires

regarding life style and alcohol consumption.

Is the mean alcohol intake for men with psoriasis (cases) greater than men without psoriasis (controls)?

Cases: mean=43, SD=85.8, n=142 Controls: mean=21, SD=34.2, n=265Poikolainen et al Br Med J 1990; 300:780-783

Page 10: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Is There a Difference? Null Hypothesis: HO

Often a statement of no treatment effect

Example 1: The proportion of red cards is the same as the proportion of black cards (50%).

Example 2: There is no association between alcohol intake and psoriasis. In other words, the mean alcohol intake for men with psoriasis is the same as the mean alcohol intake for men without psoriasis.

Page 11: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Is There a Difference? Alternative Hypothesis: HA

May be one-sided or two-sided Example 1:

One-sided: The proportion of red cards is larger than the proportion of black cards.

Two-sided: The proportion of red cards is different than the proportion of black cards.

Example 2: One-sided: Mean alcohol intake for

cases (with psoriasis) is larger than mean alcohol intake for controls (without psoriasis)

Two-sided: Mean alcohol intake for cases is different than the mean alcohol intake for controls

Page 12: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Conclusions

The null hypothesis is assumed true until evidence suggests otherwise.

2 possible conclusions: Reject the null hypothesis in favor of

the alternative. Do not reject the null hypothesis.

Page 13: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing: Errors

Significance level: Probability of rejecting a true null

hypothesis

Probability of not rejecting a false null hypothesis

Power: 1- Probability of detecting a true difference

Type I Error ()

Type II Error ()

Correct Decision

Correct Decision

DECISION

Reject HO

Do notReject HO

TRUTH

HO is False

HO is True

Page 14: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Steps Assume the null hypothesis is true. Determine a test statistic based on

the observed data. Using the test statistic, how likely is

it that we observe the outcome or something more extreme if the null hypothesis is true?

If the test statistic is unlikely under the null hypothesis, we reject the null hypothesis in favor of the alternative hypothesis.

Page 15: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:P-value

Measures how likely is it that we observe the outcome or something more extreme, assuming the null hypothesis is true.

Small p-value is evidence against the null hypothesis and we reject the null hypothesis.

Large p-value suggests the data are likely if the null hypothesis is true and we do not reject the null hypothesis.

Page 16: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:P-value Method If p < , Reject the null in favor

of the alternative hypothesis.

If p >= , Do Not Reject the null hypothesis.

p < .05 is generally considered statistically significant.

Determining the p-value requires making assumptions about the data.

Page 17: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Psoriasis Example

Ho: There is no association between alcohol intake and psoriasis.

Ha: The mean alcohol intake is different for cases and controls.

Using the test statistic, the p-value was 0.004.

Conclusion: Since the p-value is less than 0.05, Reject Ho.

There is evidence that the mean alcohol intake is higher for cases (mean=43) than controls (mean=21).

Page 18: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Antihypertensive Example Aim: Compare two

antihypertensive strategies for lowering blood pressure Double-blind, randomized study Enalapril + Felodipine vs. Enalapril 6-week treatment period 217 patients

Outcome of interest: diastolic blood pressure

Based on AJH, 1999;12:691-696.

Page 19: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Antihypertensive Example After 6 weeks of therapy, the

average change in DBP was:

10.6 mm Hg in the Enalapril + Felodipine group (n=109, SD=8.1) compared to

7.4 mm Hg in the Enalapril group (n=108, SD=6.9)

The authors used a hypothesis test to help determine which therapy was more effective.

Page 20: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing:Antihypertensive Example Statement from AJH

“The group randomized to 5 mg enalapril + 5 mg felodipine had a significantly greater reduction in trough DBP after 6 weeks of blinded therapy (10.6 mm Gh) than the group randomized to 10 mg enalapril (7.4 mm Hg, P<0.01).”

What does P<0.01 mean? Assuming that the 2 therapies are

equally effective, there is less than a 1% chance that we would have observed treatment differences as large or larger than what was observed.

Page 21: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Hypothesis Testing

Parametric methods make assumptions about the distribution of the observations.

Non-parametric methods do not make assumptions about the distribution of the observations.

The distribution of the data and the design of the study should be carefully considered when choosing the statistical test to be used.

Page 22: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data

Paired Data For each observation in the first

group, there is a corresponding observation in the second group.

Example: “Before and After”

Pairing eliminates some of the variability among individuals, since measurements are made on the same (or similar) subjects.

Paired groups are called dependent.

Page 23: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data

Paired t-test Two paired groups Sample size is large (30 or

more pairs)

Page 24: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Normal Distribution

Data follows a normal distribution if the histogram is approximately symmetric and bell shaped.

Described by two parameters mean () SD ()

Page 25: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Normal Distribution

Z-score measures how many SDs an observation is away from the mean

Z=(x-)/ About 95% of the values fall within 2

SDs of the mean

Page 26: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Paired t-test Example

In 40 subjects, blood pressure was measured before and after taking Captopril.

Outcome of interest: change in blood pressure after taking the drug

HO: No association between Captopril and blood pressure.

HA: Mean blood pressure is lower after patients take Captopril.

P-value < 0.001. Reject HO in favor of HA. There is

evidence that mean blood pressure is lower after taking Captopril.

Based on MacGregor et al., British Medical Journal, Vol. 2

Page 27: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Wilcoxon Signed Ranks Test Two paired groups Sample size is small (less than

30 pairs).

Wilcoxon Signed Ranks Test compares medians rather than means.

Non-parametric test.

Page 28: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Wilcoxon Signed Ranks Test Example In 10 postcoronary patients, maximum

oxygen uptake was measured before and after a 6 month exercise program.

Outcome of interest: change in oxygen uptake after a 6 month exercise program

Difference in max. oxygen uptake ml/(kg)(min)

5.00.0-5.0-10.0-15.0-20.0

Difference in Maximum Oxygen Uptake

Before and After Exercise Program

Fre

qu

en

cy

5

4

3

2

1

0

Std. Dev = 8.10

Mean = -5.2

N = 10.00

Page 29: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Wilcoxon Signed Ranks Test Example HO: There is no association

between exercise and oxygen uptake.

HA: Median oxygen uptake is higher after exercise program.

p-value =.09. Do not reject HO. There is not

enough evidence to conclude that oxygen uptake is higher after the exercise program.

Page 30: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Independent Samples t-test

Two independent groups Sample size is large (30 or

more in each group).

Page 31: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Independent Samples t-test Example

30 women with pregnancy-induced hypertension are given low-dose aspirin

42 women with pregnancy-induced hypertension given a placebo

Outcome of interest: blood pressure

Based on Schiff, E et al., Obstetrics and Gynecology, Vol 76, Nov 1990, 742-744.

Page 32: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Independent Samples t-test Example HO: No association between low-

dose aspirin and blood pressure. HA: Mean blood pressure is

lower for the aspirin group P-value = 0.15. Do not reject HO. There is not

enough evidence to conclude that the mean blood pressure is lower for the aspirin group.

Page 33: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Wilcoxon Rank Sum Test Two independent groups Sample size is small (less than

30).

Wilcoxon Rank Sum Test compares medians rather than means

Nonparametric test

Page 34: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 2 Groups - Continuous Data Wilcoxon Rank Sum Test Example 13 patients randomized to placebo

15 randomized to receive calcium supplements

Outcome of interest: blood pressure HO: No association between calcium

supplements and blood pressure. HA: Median blood pressure in

calcium supplement group is different than placebo group.

P-value =.79. Do not reject HO. There is not

enough evidence to conclude that median blood pressure for the calcium group is different than the placebo group.

Based on Lyle et al., JAMA, Vol 257, No 13.

Page 35: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Comparing 3 or more groups

Chi-square Test for categorical data Analysis of Variance (ANOVA) for

continuous data

Common uses: Compare an outcome for 3 or more

treatments Compare a characteristic in 3 or more

populations

Page 36: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Chi-Square Test

Compare 2 or more groups Categorical data

Example: To study effectiveness of bicycle helmets, individuals who were in an accident were studied.

Outcome of interest: Compare proportion of persons suffering a head injury while wearing a helmet to proportion of persons suffering a head injury while not wearing helmet

Page 37: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Chi-Square Test2x2 Table

12% (17/147) of those wearing a helmet had a head injury

34% (218/646) of those not wearing a helmet had a head injury

Wearing Helmet

Injury Yes No

Yes

No

17 (12%)

130 (88%)

218 (34%)

428 (66%)

Total 147 646

Page 38: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Chi-Square Test Ho: The proportion suffering a head

injury is the same for accident victims who wore helmets vs. accident victims who did not wear helmets.

Ha: The proportion suffering a head injury is different for accident victims who wore helmets vs. accident victims who did not wear helmets.

p-value < 0.001 Conclusion: Reject Ho. The

proportion of individuals suffering head injuries was higher for accident victims who did not wear helmets (34%) compared to those who did wear helmets (12%).

Among persons in an accident, wearing a helmet appears to lower incidence of head injury.

Page 39: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

ANOVA (Analysis of variance)

Used to compare a continuous variable among three or more groups

HO: The group (or treatment) means are the same.

HA: At least one mean is different from the others.

Page 40: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

One-Way ANOVA

One factor (characteristic) is being studied Example: treatment group

Placebo experimental treatment 1 experimental treatment 2

3 or more independent groups The distribution for each group is

not heavily skewed. Group variances or sample sizes

are approximately equal.

Page 41: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

One-Way ANOVAExample

Aim: Compare microbiological growth under 3 different CO2 pressure levels.

Factor of interest: 3 different CO2 pressure levels

Outcome of interest: average microbiological growth in each treatment group

HO: The mean microbiological growth for the 3 treatments (CO2 level) is the same

HA: At least one of the means is different.

p-value = .001 Reject HO in favor of HA. There is

evidence that mean growth is different for the three treatment groups.

Page 42: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

One-Way ANOVAExample

Mean microbiological growth under 3 different CO2 pressure levels. Group 1 mean: 56.2 Group 2 mean : 22.5 Group 3 mean: 26.1

Page 43: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Bonferroni Comparisons Use when ANOVA yields a

significant p-value. If we perform several t-tests to

compare each pair of means, the probability of a Type I error is > 0.05.

The Bonferroni method modifies the p-value to account for multiple comparisons so that, overall, the probability of making a Type I error is 0.05.

Page 44: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Bonferroni Comparisons Example Is the mean for group 1 different from

the mean for group 2? P=.001 Conclusion: The mean for group 1 is

different from the mean for group 2. Is the mean for group 1 different from

the mean for group 3? P=.02 Conclusion: The mean for group 1 is

different from the mean for group 3. Is the mean for group 2 different from

the mean for group 3? P=.34 Conclusion: The mean for group 2 is

different from the mean for group 3. Therefore, the difference in the 3

group means can primarily be explained by the higher mean for group 1 compared to groups 2 and 3.

Page 45: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Repeated Measures ANOVA

Subjects are measured at more than one time point

Since multiple measurements are taken for the same subject over time, the observations are not independent

Page 46: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Repeated Measures ANOVA Example 12 rabbits receive in random order

3 different dose levels of a drug to increase blood pressure, with a washout period between treatments.

Outcome of interest: average blood pressure for the three dose levels

HO: Average blood pressure is the same for the 3 dose levels

HA: At least one of the means is different.

P=0.01 Reject HO. There is evidence of a

difference in mean blood pressure for the 3 dose levels.

Page 47: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Kruskal-Wallis ANOVA

Nonparametric ANOVA

Use when the distribution for one or more groups is heavily skewed.

Page 48: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Regression

Is there a linear relation between 2 continuous variables? If so, what line best fits the data?

Use the line to predict a value for a new observation Example: Can we predict muscle based

on a woman’s age? Explore relationship between 2

numerical variables Example: What is the relation between

muscle mass and age?

Y = 148 - X

X = AGE (years)

8070605040

Y =

Me

asu

re o

f M

usc

le M

ass

120

110

100

90

80

70

60

Page 49: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Correlation (r)Is There an Association? Measures linear relationship between 2

continuous variables.

Interpreting r :

AbsoluteValue Linearof r Relationship0 - .25 poor.25 - .50 fair.50 - .75 good.75 – 1.0 very good

Page 50: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Correlation (r)Examples

r = .55r = 0

r = .85 r = -.85

Page 51: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Correlation (r)Examples

r = 1

r = -1

Page 52: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear RegressionLeast Squares Regression Line

Estimate the best line to fit the data

Y = b0 + b1X Y is the dependent variable

Example: Muscle mass X is the independent variable

Example: Age of woman

b0 is the intercept

b1 is the slope

Page 53: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Regression Example

Y = 148 - X

X = AGE (years)

8070605040

Y =

Me

asu

re o

f M

usc

le M

ass

120

110

100

90

80

70

60

Predict the muscle mass of a 60 year old woman 148 - 60 = 80

Page 54: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear Regression ExampleY = 148 - X

X = AGE (years)

8070605040

Y =

Me

asu

re o

f M

usc

le M

ass

120

110

100

90

80

70

60

On average, what is the difference in muscle mass for women who differ in age by 1 year? b1 = -1 For women whose age differs by

one year, we expect the average muscle mass will be one unit lower for the older women

Page 55: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

Linear RegressionNotes

Significant correlation does not necessarily imply causation.

Do not use a line to predict new observations if there is not significant linear correlation.

When predicting new observations, stay within the domain of the sample data.

Page 56: Introduction to Biostatistics II Jane L. Meza, Ph.D. October 24, 2005.

References

Dawson-Saunders, B and Trapp RG (1994). Basic and Clinical Biostatistics. Appleton and Lange. Norwalk, CT.

Lane, DM. (2000). Hyperstat Online. On-line text, www.statistics.com.

MacGregor GA, Markandu ND, Roulston JE and Jones JC (1979). “Essential Hypertension: Effect of an Oral Inhibitor of Angiotensin-Converting Enzyme”. British Medical Journal, Nov 3; Vol 2, 1106-9.

Neter, J., Wasserman W. and Kutner, MH. (1990). Applied Linear Statistical Models. Irwin. Burr Ridge, IL.

Pagano M and Gauvreau, K. (1993). Principles of Biostatistics. Duxbury Press. Belmont, CA.

Schiff E, Barkai G, Ben-Baruch G and Mashiach S. (1990). “Low-Dose Aspirin Does Not Influence the Clinical Course of Women with Mild Pregnancy-Induced Hypertension”. Obstetrics and Gynecology, Vol 76, November, 742-744.

Swinscow, TDV. (1997). Statistics at Square One. BMJ Publishing Group. On-line text, www.statistics.com.

Triola MF (1998), Elementary Statistics. Addison-Wesley. Reading, MS.