Biostatistics Case Studies 2006 Peter D. Christenson Biostatistician Session 2: Correlation of Time Courses of Simultaneous.

Slides:



Advertisements
Similar presentations
Irwin/McGraw-Hill © Andrew F. Siegel, 1997 and l Chapter 12 l Multiple Regression: Predicting One Factor from Several Others.
Advertisements

Linear Regression t-Tests Cardiovascular fitness among skiers.
1 SSS II Lecture 1: Correlation and Regression Graduate School 2008/2009 Social Science Statistics II Gwilym Pryce
Chapter 8 Linear Regression © 2010 Pearson Education 1.
Objectives (BPS chapter 24)
2.2 Correlation Correlation measures the direction and strength of the linear relationship between two quantitative variables.
EPIDEMIOLOGY AND BIOSTATISTICS DEPT Esimating Population Value with Hypothesis Testing.
Statistics for the Social Sciences
Introduction to Hypothesis Testing
Fall 2006 – Fundamentals of Business Statistics 1 Chapter 13 Introduction to Linear Regression and Correlation Analysis.
REGRESSION AND CORRELATION
Stat 112: Lecture 9 Notes Homework 3: Due next Thursday
Review for Exam 2 Some important themes from Chapters 6-9 Chap. 6. Significance Tests Chap. 7: Comparing Two Groups Chap. 8: Contingency Tables (Categorical.
Review for Final Exam Some important themes from Chapters 9-11 Final exam covers these chapters, but implicitly tests the entire course, because we use.
1 Chapter 10 Correlation and Regression We deal with two variables, x and y. Main goal: Investigate how x and y are related, or correlated; how much they.
Analysis of Clustered and Longitudinal Data
1 1 Slide © 2008 Thomson South-Western. All Rights Reserved Slides by JOHN LOUCKS & Updated by SPIROS VELIANITIS.
Standard Error of the Mean
Objectives of Multiple Regression
Inference for regression - Simple linear regression
Chapter 13: Inference in Regression
Correlation and regression 1: Correlation Coefficient
GCSE Data Handling Coursework 1 Examining the Data examine carefully the data you are given it’s important to get a feel for the raw data before you use.
Biostatistics in Practice Peter D. Christenson Biostatistician LABioMed.org /Biostat Session 5: Methods for Assessing Associations.
September In Chapter 14: 14.1 Data 14.2 Scatterplots 14.3 Correlation 14.4 Regression.
BPS - 3rd Ed. Chapter 211 Inference for Regression.
Inference for Linear Regression Conditions for Regression Inference: Suppose we have n observations on an explanatory variable x and a response variable.
Lecture 14 Sections 7.1 – 7.2 Objectives:
Biostatistics in Practice Peter D. Christenson Biostatistician Session 5: Associations and Confounding.
Section Copyright © 2014, 2012, 2010 Pearson Education, Inc. Lecture Slides Elementary Statistics Twelfth Edition and the Triola Statistics Series.
Copyright © 2010 Pearson Education, Inc Chapter Seventeen Correlation and Regression.
Biostatistics in Practice Peter D. Christenson Biostatistician Session 5: Methods for Assessing Associations.
1 Chapter 10 Correlation and Regression 10.2 Correlation 10.3 Regression.
Biostatistics Case Studies 2008 Peter D. Christenson Biostatistician Session 3: Replicates.
Biostatistics in Practice Peter D. Christenson Biostatistician LABioMed.org /Biostat Session 6: Case Study.
Biostatistics Case Studies 2007 Peter D. Christenson Biostatistician Session 3: Incomplete Data in Longitudinal Studies.
Chapter 10 Correlation and Regression
Chapter 1 Introduction to Statistics. Statistical Methods Were developed to serve a purpose Were developed to serve a purpose The purpose for each statistical.
Biostatistics Case Studies 2008 Peter D. Christenson Biostatistician Session 5: Choices for Longitudinal Data Analysis.
7. Comparing Two Groups Goal: Use CI and/or significance test to compare means (quantitative variable) proportions (categorical variable) Group 1 Group.
Managerial Economics Demand Estimation & Forecasting.
Lecture 8 Simple Linear Regression (cont.). Section Objectives: Statistical model for linear regression Data for simple linear regression Estimation.
MGS3100_04.ppt/Sep 29, 2015/Page 1 Georgia State University - Confidential MGS 3100 Business Analysis Regression Sep 29 and 30, 2015.
Biostatistics Case Studies 2008 Peter D. Christenson Biostatistician Session 2: Statistical Adjustment: How it Works.
Objectives 2.1Scatterplots  Scatterplots  Explanatory and response variables  Interpreting scatterplots  Outliers Adapted from authors’ slides © 2012.
Biostatistics in Practice Peter D. Christenson Biostatistician LABioMed.org /Biostat Session 4: Study Size and Power.
Biostatistics in Practice Peter D. Christenson Biostatistician Session 4: Study Size and Power.
Biostatistics Case Studies 2006 Peter D. Christenson Biostatistician Session 6: Discrepancies as Predictors: Discrepancy.
Biostatistics Case Studies 2005 Peter D. Christenson Biostatistician Session 6: “Number Needed to Treat” to Prevent One Case.
Biostatistics in Practice Peter D. Christenson Biostatistician Session 6: Case Study.
Biostatistics Case Studies 2010 Peter D. Christenson Biostatistician Session 3: Clustering and Experimental Replicates.
Biostatistics in Practice Peter D. Christenson Biostatistician Session 3: Testing Hypotheses.
 Find the Least Squares Regression Line and interpret its slope, y-intercept, and the coefficients of correlation and determination  Justify the regression.
Biostatistics in Practice Peter D. Christenson Biostatistician Session 4: Study Size for Precision or Power.
Chapter 8: Simple Linear Regression Yang Zhenlin.
Session 6: Other Analysis Issues In this session, we consider various analysis issues that occur in practice: Incomplete Data: –Subjects drop-out, do not.
Sampling Design and Analysis MTH 494 Lecture-21 Ossam Chohan Assistant Professor CIIT Abbottabad.
1 HETEROSCEDASTICITY: WEIGHTED AND LOGARITHMIC REGRESSIONS This sequence presents two methods for dealing with the problem of heteroscedasticity. We will.
Uncertainty and confidence Although the sample mean,, is a unique number for any particular sample, if you pick a different sample you will probably get.
Regression Analysis Presentation 13. Regression In Chapter 15, we looked at associations between two categorical variables. We will now focus on relationships.
Copyright © 2009 Pearson Education, Inc. 9.2 Hypothesis Tests for Population Means LEARNING GOAL Understand and interpret one- and two-tailed hypothesis.
Copyright © Cengage Learning. All rights reserved. 8 9 Correlation and Regression.
BPS - 5th Ed. Chapter 231 Inference for Regression.
Chapter 4 More on Two-Variable Data. Four Corners Play a game of four corners, selecting the corner each time by rolling a die Collect the data in a table.
Describing Bivariate Relationships. Bivariate Relationships When exploring/describing a bivariate (x,y) relationship: Determine the Explanatory and Response.
Theme 6. Linear regression
26134 Business Statistics Week 5 Tutorial
CHAPTER 29: Multiple Regression*
Basic Practice of Statistics - 3rd Edition Inference for Regression
MGS 3100 Business Analysis Regression Feb 18, 2016
Presentation transcript:

Biostatistics Case Studies 2006 Peter D. Christenson Biostatistician Session 2: Correlation of Time Courses of Simultaneous Measures

Case Study

Time Courses of Four Measures Fig 2AFig 1A Fig 2BFig 1B -2 hr 0-10 min hr

Possible Analyses for Correlation of Time Trends 1.Entrainment Usually with known functional relations. Focus on parameters of differential equations, or known cyclic, circadian pattern: phase, amplitude, freq, e.g., melatonin, hormones. 2.Time trend for one measure, adjusted for another measure Focus on expected behavior over time if 2 nd measure had remained constant. 3.Time trend of ratio of two measures 4.Random coefficient modeling – this paper Time is used to pair measures, then ignored. Approximates correlating the two measures for each individual separately, then summarizing over them.

Ratios Over Time Ratio may have a biological meaning for particular measures: OK. Potential scaling problems: Time Y Z Z/Y Could use Δs, percentiles, Z-scores to obtain an appropriate ratio in some situations.

Ratios Over Time, Continued Even with appropriate scaling, as below, coupling corresponds to no change in ratio. Want to prove a negative pattern for the ratio. Time Y Z Y/Z Remember last session: proving equivalence vs. proving difference vs. observing minimal difference. Margin of Equivalence

Simulated Data We first look at some data that I generated: only 5 sheep, all treated the same. mean measures every hour for 8 hours. Data is NOT what actually occurred in this experiment. These data: have a similar overall pattern for two time courses. have a correlation of patterns that seems contradictory. show a problem too extreme to be common. show a problem that is still a problem that cannot be ignored.

Simulated Data: Time Pattern 1

Simulated Data: Time Pattern 2

Simulated Data: Correlation

Simulated Data Thus, Blood flow ↑ over time, as in the paper. PO2 ↓ over time, as in the paper. Blood flow and PO2 appear positively correlated in the graph which is supported by analysis: correlation = 0.82 with p< blood flow ↑ by a mean 7.2 for each 1 mmHg increase in PO2 (95% CI: 5.5 to 8.9): Effect Estimate Std Error p-value Lower Upper Intercept o < What is the explanation?

Simulated Data: Graphical Explanation Each individual fetus does indeed have an inverse relation:

Simulated Data: Statistical Agreement on the Graphical Explanation After specifying individual fetuses in the analysis: Effect Estimate Std Error p-value Lower Upper Intercept Slope < So, Blood flow and PO2 are negatively correlated within any individual, averaging: blood flow ↓ by a mean 3.4 for each 1 mmHg increase in PO2 (95% CI: 2.2 to 4.6).

Simulated Data: An Extreme Illustration of Real Issues My simulation is unrealistic because usually a pattern among different individuals in a population also occurs when the measures change within individuals: “Among recapitulates within”? A reminder that correlations between measures always depend on the ranges of the measures. The following slide shows the authors’ use of this method. Note that : They did not have the extreme reversal that I simulated. The bloodflow-O2 relation would have been biased to be stronger if they had ignored sheep differences.

Correlation of Actual Carotid Blood Flow and Cortical Tissue O 2 in the Paper Fig 3A Fig 2A Fig 1A

Further Comments on Individual Slopes This paper only reported R 2 =0.69, p< for the bloodflow-O2 relation in Fig 3A. The estimate of the average slope and it’s CI is usually more informative. Some investigators use a standard regression for each individual and then find the mean and SE of these slopes. A mixed model should be used if: Some individuals have only a few pairs of data, so that their slopes are poorly estimated. All individuals have many pairs of data, but the # varies among individuals, so that individual slopes need to be weighted according to their amount of information.

Coupling of Cortical and Carotid Blood Flows Fig 2A Fig 2B Fig 3B Statistically, this is the same as the previous analysis with O2.

Time Trends for Each Measure Need to Account for Individual Sheep Recall Time Trend: Any reasonable person would say there is an obvious trend.

Time Trends for Each Measure Need to Account for Individual Sheep Incorrect Analysis Slope Estimate: 2.8 ± % CI: to 6.84 p-value = 0.17 Repeated Measures Analysis Slope Estimate: 2.8 ± % CI: 2.38 to 3.20 p-value < Mean PatternPatterns for Individuals

Self Quiz 1.T or F: If two measures are recorded over time, the ratio of two measures at each time is a good way to assess whether they are correlated. 2.Explain why an X-Y scatterplot of two measures recorded for each of several individuals, but at different times for each individual, can be misleading. 3.Could the problem in (2) remain if every subject is measured at the same times? 4.Suppose you use separate regressions for each subject measured at multiple times to find the rate of change of one measure for a 1-unit change in the other for each subject. Give at least one reason why averaging these slopes over subjects could be misleading. 5.Does the authors’ analysis in Fig 3A account for the fact that fetuses have different pre-asphyxia bloodflow and O2?