A STUDY OF DETERMINANTS OF PLASMA RETINOL AND BETA-CAROTENE Tutor: Dr. Kaibo Wang Applied...

49
A STUDY OF DETERMINANTS OF PLASMA RETINOL AND BETA-CAROTENE Tutor: Dr. Kaibo Wang Applied Statistics, Industrial Engineering, Tsinghua University Team member: Wang Jun 2009210552 Cui Wen 2009210554 Sun Ningning 2009210571 Lv Shikun 2009210566

Transcript of A STUDY OF DETERMINANTS OF PLASMA RETINOL AND BETA-CAROTENE Tutor: Dr. Kaibo Wang Applied...

A STUDY OF DETERMINANTS OF PLASMA RETINOL AND BETA-CAROTENE

Tutor: Dr. Kaibo Wang

Applied Statistics, Industrial Engineering, Tsinghua University

Team member: – Wang Jun 2009210552 Cui Wen 2009210554

– Sun Ningning 2009210571 Lv Shikun 2009210566

Page 2

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 3

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 4

INTRODUCTION

Past research: low dietary intake or low plasma concentrations of retinol, beta-carotene, or other carotenoids might be associated with increased risk of developing certain types of cancer.

Cross-sectional study: to investigate the relationship between personal characteristics and dietary factors, and plasma concentrations of retinol, beta-carotene and other carotenoids.

Experimernt: – N=315

– Patients:

• Had an elective surgical procedure during a three-year period

• Removed a lesion of the lung, colon, breast, skin, ovary or uterus

• Non-cancerous

Page 5

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 6

1 、 Observational studies have suggested that low dietary intake or low plasma

concentrations of retinol, beta-carotene, or other carotenoids might be

associated with increased risk of developing certain types of cancer ;

2 、 The relationship between plasma carotenoids, plasma cholesterol, cigarette

smoking, vitamin supplement use, and intakes of alcohol, vitamin A, and

carotene were investigated in 1981 by in the research of Russell-Briefel R ;

3 、 The relationship of diet and nutritional supplements, cigarette use, alcohol

consumption, and blood lipids to plasma levels of beta-carotene was studied

among 330 men and women aged 18–79 years in the research of Stryker WS.

LITERATURE REWIEW

Page 7

1 、 Many epidemiologic studies have been conducted primarily as dietary studies

of vitamin A and carotene, or as blood studies of serum retinol.

2 、 Willett WC showed that, with higher levels of retinol plasma, the risks of get

cancer may be decreased. However, plasma retinol levels are under strict

control and a high intake of preformed vitamin does not seem to be relevant

for cancer prevention;

3 、 Stähelin, H. B. suggested an inverse relationship between vitamin A and

cancer risk, although some studies have found no relationship. Then people

find that a lower retinol levels is not the cause of an invasive cancer. Instead,

it is the cancer that brings about a lower retinol level in human body;

LITERATURE REWIEW

Page 8

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 9

PURPOSE OF THE STUDY

Tofind out internal factors which may have some effect or relationship with the beta-carotene and retinol in people’s plasma.

– Age (years)

– Quetelet:

– Number of calories consumed per day.

– Grams of fat consumed per day.

– Grams of fiber consumed per day.

– Number of alcoholic drinks consumed per week.

– Cholesterol consumed (mg per day).

– Dietary beta-carotene consumed (mcg per day).

– Dietary retinol consumed (mcg per day)

– Sex (1=Male, 2=Female).

– Smoking status (1=Never, 2=Former, 3=Current Smoker)

– Vitamin Use (1=Yes, fairly often, 2=Yes, not often, 3=No)

Page 10

PURPOSE OF THE STUDY

Page 11

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 12

Content:

1. Variables Types and Levels

Quantitative variables & Categorical variables

2. Descriptive Analysis

For all 12 independent variables, with:

Summary Statistics/Histogram/Scatter Plot

3. Data Analysis via Regression & General Linear Model

3.1 BETA-CAROTENE

3.2 RETINOL

ANALYSYS RESULTS

Page 13

Variable: SEX

1 : Male 2 : Female

Plasma Retinol: Male is higher than female

Beta-Carotene: Female is a little higher and more outliers

2.Descriptive Analysis

Page 14

Variable: VITUSE(Vitamin use)

1=Yes, fairly often, 2=Yes, not often, 3=No

Plasma Retinol: No much difference, almost in the same level

Beta-Carotene: Often users>Not-often users>Non-users

2.Descriptive Analysis

Page 15

Variable: SMOKSTAT(Smoking Status)

1=Never, 2=Former, 3=Current Smoker

Plasma Retinol: Former smokers has the highest level

Beta-Carotene: Never smokers contains higher level

2.Descriptive Analysis

Page 16

An example for continuous variables

2.Descriptive Analysis

Mean StDev Min Q1 Median Q3 Max

Age 50.146 14.575 19.000 39.000 48.000 63.000 83.000

Page 17

Variable : AGE, QUETELET , CALORIES

AGE(age): Most in the area between 32 and 77who are basically middle-age or elderly people.

QUETELET( ): Most between 18.5 and 30 who are normal and some are a little overweight.

CALORIES(calories): Most are concentrated between 1000 and 2200.

2.Descriptive Analysis

Page 18

Variable: QUETELET( )

Standard category from WHO:

Quetelet is a statistical measurement which compares a person's weight and height.

2.Descriptive Analysis

Category BMI range – kg/m2

Severely

underweight

less than 16.5

Underweight from 16.5 to 18.4

Normal from 18.5 to 24.9

Overweight from 25 to 30

Obese Class I from 30.1 to 34.9

Obese Class II from 35 to 40

Obese Class III over 40

Page 19

Variable: FAT, FIBER, ALCOHOL

FAT: Grams of fat consumed per day. Most are between 45 and 135.

FIBER: Grams of fiber consumed per day. Between 6 and 18

ALCOHOL: Number of alcoholic drinks consumed per week. Most rarely drink, but there is an obvious outlier, which reaches 203 alcohol per week.

2.Descriptive Analysis

Page 20

Variable: CHOLESTEROL, BETADIET, RETDIET

CHOLESTEROL: milligram of cholesterol consumed per day

BETADIET : microgram of dietary beta-carotene consumed per day

RETDIET : microgram of dietary retinol consumed per day

Most are between 500 and 1500.

2.Descriptive Analysis

Page 21

3.1 data analysis about BETA-CAROTENE

AGEQUETELETCALORIES

FATFIBER

ALCOHOLCHOLESTEROL

BETADIETRETDIET

SEXSMOKSTAT

VITUSE

Beta-carotene content in

plasma1 、 Regression2 、 GLM

Page 22

Steps of Regression:

1 、 Check data distribution through scatter plots

2 、 Best subset and stepwise regression to select predictors

3 、 Do regression and residual check

4 、 Do transformation

5 、 The final model

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 23

1 、 Check data distribution through scatter plots

transformation can not avoid data aggregations, and therefore delete the outliers

906030 4000200001600

800

090

60

30

50

35

20

16008000

4000

2000

0

503520

Pl asma beta- carotene

Age

Quetel et

CALORI ES

Pl asma beta- carotene, Age, Quetel et, CALORI ES 的矩阵图

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 24

2 、 Use best subset and stepwise regression to select predictors Use dummy variables to take place of discreet variables:

SEX, SMOKSTAT and VITUSE

Result of stepwise regression :

Variables T-Value P-value

QUETLET -4.11 0.000

BETADIET 3.57 0.000

Vitamin_status_3 -3.17 0.002

Smoking_status_3 -2.04 0.042

FAT -1.88 0.061

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 25

3 、 Do regression and residual check

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 26

4 、 Do transformation use log (plasma beta-carotene) to replace plasma beta-carotene

Redo step1—step3

Variables P-value coefficient

QUETLET 0.000 -0.0140

BETADIET 0.054 0.000025

Vitamin_st

atus_30.001 -0.124

Smoking_

status_30.023 -0.116

FAT 0.048 -0.00113

AGE 0.046 0.00248

Sex_2 0.085 0.0934

FIBER 0.132 0.00632

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 27

5 、 The final model

Log (plasma beta-carotene) = 2.32 - 0.0140QUETLET -

0.124vitamin_status_3- 0.116 smoking_status_3 +

0.000025 BETADIET - 0.00113 FAT+ 0.00248 AGE+

0.0934 sex_2 + 0.00632 FIBER

3.1.1 data analysis via Regression ( BETA-CAROTENE )

Page 28

Steps of GLM:

1 、 Check data distribution through scatter plots

2 、 Select predictors by trial

3 、 GLM model

4 、 Residual check

3.1.2 data analysis via GLM ( BETA-CAROTENE )

Page 29

1 、 Check data distribution through scatter plots

similar to step 1 of regression

2 、 Select predictors by trial

Variables P-value coefficient

AGE 0.090 0.002224

QUETLET 0.000 -0.014010

CALORIES 0.385 -0.000082

FAT 0.758 0.000447

FIBER 0.139 0.00818

ALCOHOL 0.750 0.001381

CHOLESTEROL 0.603 -0.000109

BETADIET 0.111 0.000021

RETDIET 0.337 0.000033BETADIET*Vitami

n

Vitamin_1 0.027 0.000034

Vitamin_2 0.858 0.000003

3.1.2 data analysis via GLM ( BETA-CAROTENE )

Page 30

3 、 GLM model

Log (plasma beta-carotene) =2.3061+0.002224 AGE-

0.014010QUETLET+0.00818FIBER+0.000021BETADIE

T+0.000034BETADIET*Vitamin_1

3.1.2 data analysis via GLM ( BETA-CAROTENE )

Page 31

4 、 Residual check

3.1.2 data analysis via GLM ( BETA-CAROTENE )

Page 32

Conclusion :

1 、 The coefficient of QUETLET, vitamin_status_3, smoking_status_3 and FAT are

negative, which indicates that with the increase of these variables, there would

be a decrease of the content of beta-carotene in plasma;

2 、 The coefficient of BETADIET, AGE, Sex_2 and FIBER are positive, which

indicates that with the increase of average number of these variables, there

would also be an increase of the content of beta-carotene in plasma.

Log (plasma beta-carotene) = 2.32 - 0.0140QUETLET -

0.124vitamin_status_3- 0.116 smoking_status_3 + 0.000025 BETADIET -

0.00113 FAT+ 0.00248 AGE+ 0.0934 sex_2 + 0.00632 FIBER

3.1 data analysis about BETA-CAROTENE

Page 33

Steps of Regression:

1 、 Check data distribution through scatter plots

2 、 Best subset and stepwise regression (3 methods) to select predictors

3 、 Do regression and residual check

4 、 Draw conclusion

3.2.1 data analysis via Regression ( RETINOL )

Page 34

1 、 Check data distribution through scatter plots

3.2.1 data analysis via Regression ( RETINOL )

Page 35

1 、 Check data distribution through scatter plots

3.2.1 data analysis via Regression ( RETINOL )

Page 36

2 、 Use best subset and stepwise regression to select predictors Using dummy variables to transform the Categorical variables

Define SEX_F=SEX-1, so SEX_F=1, when SEX=Female; SEX_F=0, when SEX=Male.

3.2.1 data analysis via Regression ( RETINOL )

SMOKSTAT SMOK_1 SMOK_2

1 0 0

2 0 1

3 1 0

VITUSE VITUSE _1 VITUSE _21 0 0

2 0 1

3 1 0

Page 37

2 、 Use best subset and stepwise regression to select predictors Select 7 variables :

AGE, QUETELET, ALCOHOL, BETADIET, SEX_F, SMOK_2, and VITUSE_1

Result of stepwise regression :

3.2.1 data analysis via Regression ( RETINOL )

Variables T-Value P-value

AGE 3.32 0.002

QUETELET 1.72 0.295

ALCOHOL 3.24 0.053

BETADIET -2.04 0.031

SEX_F -1.97 0.027

SMOK_2 1.70 0.035

VITUSE_1 -2.95 0.033

R-sq.= 13.55; R-Sq.(adj)=11.42

Page 38

2 、 Use best subset and stepwise regression to select predictors The model is :

3.2.1 data analysis via Regression ( RETINOL )

RETPLASMA = 517 + 2.09 AGE - 0.0149 BETADIET+5.228 ALCOHOL- 71.7 SEX_F + 41.9 SMOK_2 - 43.4 VITUSE_1

Page 39

Steps of GLM:

1 、 Select interaction predictors by trial

2 、 GLM model

3 、 Residual check

3.2.2 data analysis via GLM ( RETINAL )

Page 40

1 、 Select predictors by trial

Finally find no interaction predictor.

3.2.2 data analysis via GLM ( RETINAL )

Variables T-Value P-value

Constant 6.57 0.000

AGE 2.50 0.013

QUETLET 0.90 0.370

CALORIES -0.70 0.486

FAT -1.43 0.153

FIBER -0.79 0.428

ALCOHOL 1.77 0.079

CHOLESTEROL 0.92 0.360

BETADIET -1.66 0.097

RETDIET 0.40 0.688

R-sq.= 14.75%; R-Sq.(adj)= 9.52%

Page 41

3 、 GLM model

3.2.2 data analysis via GLM ( RETINAL )

RETPLASMA=510.86+1.8777AGE+5.002ALCOHOL-0.013507BETADIET

Page 42

4 、 Residual check

3.2.2 data analysis via GLM ( RETINAL )

5002500-250-500

99. 9

99

90

50

10

1

0. 1

Resi dual

Percent

800700600500400

400

200

0

-200

-400

Fi tted Val ue

Residual

4003002001000-100-200-300

40

30

20

10

0

Resi dual

Frequency

260240220200180160140120100806040201

400

200

0

-200

-400

Observati on Order

Residual

Normal Probabi l i ty Pl ot Versus Fi ts

Hi stogram Versus Order

Resi dual Pl ots for RETPLASMA

Page 43

Conclusion :

1. The coefficient of AGE is positive in both models, indicating that as people get

older, the plasma retinal level will raise.

2. Both model shows that people drink more wine will have higher plasma retinal

level. But the data of ALCOHOL is almost all less than 10, so its influence is

not obivous.

3.2.2 data analysis via GLM ( RETINAL )

RETPLASMA = 517 + 2.09 AGE +5.228 ALCOHOL- 0.0149 BETADIET- 71.7 SEX_F + 41.9 SMOK_2 - 43.4 VITUSE_1

RETPLASMA=510.86+1.8777AGE+5.002ALCOHOL-0.013507BETADIET

Regression:

GLM:

Page 44

3.2.2 data analysis via GLM ( RETINAL )

RETPLASMA = 517 + 2.09 AGE +5.228 ALCOHOL- 0.0149 BETADIET- 71.7 SEX_F + 41.9 SMOK_2 - 43.4 VITUSE_1

RETPLASMA=510.86+1.8777AGE+5.002ALCOHOL-0.013507BETADIET

Regression:

GLM:

Conclusion :

3. The coefficient of BETADIET is negative in both models, which means that

people consuming more beta-carotene have lower level of plasma retinal. So

balance of different vitamin is very important.

4. The coefficient of 3 dummy variables in regression model is -71.7, 41.9 and -

43.4, indicating women’s average plasma retinal level is lower than men’s.

People who are former smokers or never use vitamin have lower plasma retinal

level .

Page 45

We conclude that there is wide variability in plasma concentrations

of these micronutrients in humans, and that much of this variability is

associated with dietary habits and personal characteristics. A better

understanding of the physiological relationship between some personal

characteristics and plasma concentrations of these micronutrients will

require further study.

Discussion

Page 46

I. INTRODUCTION

II. LITERATURE REWIEW

III. PURPOSE OF THE STUDY

IV. ANALYSYS RESULTS

V. REFERANCE

Outline

Page 47

Peto R, Doll R, Buckley JD, et al. Can dietary beta-carotene materially reduce human cancer rates? Nature 1981;290:201-8.

Russell-Briefel R, Bates MW, Kuller LH. The relationship of plasma carotenoids to health andbiochemical factors in middle-aged men. Am J Epidemiol 1986;122:741-9.

Stryker WS, Kaplan LA, Stein EA, et al. The relation of diet, cigarette smoking, and alcohol consumption to plasma beta-carotene and alphatocopherol levels. Am J Epidemiol 1988;127:283- 96.

Adams-Campbell, L. L., M. U. Nwankwo, et al. (1992). Serum retinol, carotenoids, vitamin E, and cholesterol in Nigerian women. Nutritional Biochemistry 3(2): 58-61.

REFERANCE

Page 48

Comstock, G. W., M. S. Menkes, et al. (1988). Serum levels of retinol, beta-carotene, and alpha-tocopherol in older adults.American Journal of Epidemiology 127(1): 114-123.

Russellbriefel, R., M. W. Bates, et al. (1985). The relationship of plasma carotenoids to health and biohchemical factors in middle-aged men. American Journal of Epidemiology 122(5): 741-749.

Stähelin, H. B., E. Buess, et al. (1982). vitamin A, cardiovascular risk factors, and mortality. The Lancet 319(8268): 394-395.

Van Poppel, G. and H. van den Berg (1997). Vitamins and cancer. Cancer Letters 114(1-2): 195-202.

REFERANCE

Page 49

Thank YouFor

For Attention