|Sample size requirements for case-control study designs.|
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|PMID: 11747473 Owner: NLM Status: MEDLINE|
|BACKGROUND: Published formulas for case-control designs provide sample sizes required to determine that a given disease-exposure odds ratio is significantly different from one, adjusting for a potential confounder and possible interaction. RESULTS: The formulas are extended from one control per case to F controls per case and adjusted for a potential multi-category confounder in unmatched or matched designs. Interactive FORTRAN programs are described which compute the formulas. The effect of potential disease-exposure-confounder interaction may be explored. CONCLUSIONS: Software is now available for computing adjusted sample sizes for case-control designs.|
|M D Edwardes|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2001-11-19|
|Title: BMC medical research methodology Volume: 1 ISSN: 1471-2288 ISO Abbreviation: BMC Med Res Methodol Publication Date: 2001|
|Created Date: 2003-10-29 Completed Date: 2003-12-16 Revised Date: 2009-11-18|
Medline Journal Info:
|Nlm Unique ID: 100968545 Medline TA: BMC Med Res Methodol Country: England|
|Languages: eng Pagination: 11 Citation Subset: IM|
|Division of Clinical Epidemiology, Royal Victoria Hospital, Montreal, Quebec, Canada. firstname.lastname@example.org|
|APA/MLA Format Download EndNote Download BibTex|
Research Design / statistics & numerical data*
Software / statistics & numerical data
|BMC Med Res Methodol. 2002;2(1):16
Journal ID (nlm-ta): BMC Med Res Methodol
Publisher: BioMed Central, London
Copyright ? 2001 Edwardes; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
Received Day: 19 Month: 7 Year: 2001
Accepted Day: 19 Month: 11 Year: 2001
collection publication date: Year: 2001
Electronic publication date: Day: 19 Month: 11 Year: 2001
Volume: 1First Page: 11 Last Page: 11
Publisher Id: 1471-2288-1-11
PubMed Id: 11747473
|Sample size requirements for case-control study designs|
|Michael D Edwardes1||Email: email@example.com|
1Division of Clinical Epidemiology, Royal Victoria Hospital, Montreal, Quebec, Canada
Breslow and Day  and Smith and Day  provide asymptotic formulas for the computation of case-control sample sizes required for odds ratios, unadjusted or adjusted for a confounder  and for stratified matched designs . The notation we use is their notation. Their formulas are extended here to include more than one control per case. The formulas for stratified matched were deduced from applying the approach of Breslow and Day  (pages 305?6) to Table 7 of . Modification of the formulas for specified interactions [1,3] is also shown. These formulas are based on the logarithm of the odds ratio, for which the normal approximation is more accurate than for the exposure difference, so these formulas are more accurate than the exposure difference formula that is given in the majority of general methods references [4,5].
Two conversational FORTRAN programs, DAYSMITH and DESIGN, compute the formulas. They were submitted to STATLIB for non-commercial distribution a few years ago, and are obtained with an e-mail message such as "send design.exe from general" to . The programs produce a table of numbers of cases and controls required for a variety of specifications of Type I and Type II error, adjusted for the confounder, unadjusted, and adjusted for stratified matching, with the strata being the levels of the confounder. The two programs have different input requirements. Program DAYSMITH asks for exactly the items required for the Smith and Day formulas. Program DESIGN accepts alternative input that is converted in the program to the items required for the same formulas. The formulas used are shown in Appendix 1.
The sample sizes computed are for the detection of a given disease-exposure odds ratio, that is, the sample sizes at which a certain statistical test will reject the null hypothesis that the odds ratio is one. The input items are as follows:
RE = the odds ratio to be detected (typically a minimum value),
S = 1 or 2 for one-sided or two-sided type I error,
F = the number of controls per case,
P = the control population exposure probability, and
I = an indicator to request interaction adjustment.
Roughly speaking, interaction in statistics corresponds to effect modification in epidemiology. By not selecting an interaction adjustment, we effectively assume that the disease-exposure odds ratio does not differ across confounder levels. Interaction is discussed further below.
The number of confounder levels, denoted K is asked for next. If K = 1, unadjusted sample sizes only are computed, and no other input is required. Program DESIGN is identical to this point. For most applications, no confounder adjustment is required and so the program returns unadjusted sample sizes and is finished after a 1 is entered for K. The unadjusted formula  is more accurate than the usual unadjusted formulas [4,5], and may therefore produce different sample sizes than those.
If K > 1, one of the levels of the confounder is taken to be a reference level, and is referred to as level one. The order of the levels is otherwise immaterial. The input required next is three numbers for each of the K?1 remaining levels, p1i, p2i, and RCi, i = 2,..., K, which are
p1i = Pr(Ci|E) = among the exposed population, the proportion at level i of the confounder,
= among the unexposed population, the proportion at level i of the confounder, and
RCi = the disease-confounder odds ratio (with confounder level i versus level 1).
For the reference level, we set Rc1 = 1 for the formulas that follow. We compute
Whereas DAYSMITH asks for the same input as requested in the original references [1-3], we found that alternative input made more sense for our initial applications [6,7], so a second program was written. The input for DESIGN is the same as for DAYSMITH up to the point after which the number of levels of the confounder, K, is asked for.
Again, one of the levels of the confounder is taken to be a reference level, and is referred to as level one. The input that is required next is one number for the reference level, ri, and then three (four when interaction is included) numbers for each of the K?1 remaining levels, ri, pi, and RCi, i = 2,...,K, which are
ri = Pr(E|Ci) = the probability of exposure at level i of the confounder,
pi = Pr(Ci) = the probability of being in level i of the confounder, and
RCi = the odds ratio of disease and confounder level i (versus level 1).
For the reference level, we again set RCi = 1.
From Bayes Theorem, we compute
p2i=(1 ? ri)pi/(1 ? P).
We have one more input item than is actually required, and that is used for a check, where we can use the fact that
What we actually do is check the sum
The sum ? is supposed to be equal to one. If it is not one, then we re-define and report
unless they are negative. An alternative used in earlier versions was to compute
for j = 1,2 and i = 1,...,K. This is equivalent to replacing
i = 1,..., K, which is how the program used to report the change.
The following example is one of several computations performed for a published research protocol for a study of the association of oral contraceptive (OC) use with cardiovascular risks, controlling for age group . A related protocol  has smoking as a confounder.
The numbers entered for P, ri, pi, and RCi, i = 2,...,K, are all taken from the Saskatchewan government medical database, which includes the entire population from which a case-control sample is to be taken. In many applications, such numbers are not available from a reliable source. In that case, one may try sets of alternative minimum and maximum numbers for a range of results. The maximum sample sizes obtained from such sensitivity analyses would be the conservative recommendation.
Both programs first request RE to I. For RE, the outcome of interest is hospitalisation due to certain cardiovascular risks. The exposure is a specific OC with 10% of the market share . Since overall OC prevalence is 30%, then P = .03 for that specific OC. Using > to denote the cursor for computer entry, we type:
>2 2 3 .03 0
for RE, S, F, P and I, respectively, then press enter. We then receive the message:
Type the number of confounder levels, and <enter>. Type 1 if no confounder.
We enter 5 levels and press enter.
Now type in the population exposure probability for the reference level of the confounding variable.
This will be put at level 1, so it is Pr(E|C1)
The confounder levels are five age groups, and level 1 corresponds to the youngest age group 15?21, for which we enter the prevalence for a specific OC with 10% of the market share. We type .055 and press enter.
The reply is:
Now type in, for each of the other 4 level(s) of the confounding variable, Pr(E|Ci), Pr(Ci), and Rc(i), separated by at least one blank or <enter>, where Pr(E|Ci) = in the population at level i of the confounder, the proportion exposed, Pr(Ci) = the probability of being at level i, and Rc(i) = odds ratio of disease and confounder level i (versus level 1).
The following numbers are entered for age groups 22?26, 27?31, 22?39 and 40+:
> .038 .24 2
> .021 .2 8
> .008 .18 8
> .004 .15 28.5
Note that Rc(5) = RC5 = 28.5, a very high value. That is to be expected if all older women are included. (For the final protocol , a cut-off was made at age 45.) When enter is pressed, we receive some confirmation of the input, and a message that the result is written to file design.out. That is, as currently written, the sample sizes and other output are not automatically shown on the screen, but are saved in "design.out" to be viewed directly there. Appendix 2 (Second attached file, app2.txt, a text file) shows the output from the preceding session, which includes a correction of the input values.
Looking at Appendix 2, we see unadjusted sample sizes, those adjusted for age in an unmatched study, and a third set of sample sizes for a matched case-control study. For our example , both unmatched and matched designs are considered. With the low value of P and the high value RC5, we see that a large difference in sample sizes required for either design may result. In most applications, however, the differences are not so dramatic.
Epidemiological literature usually gives formulas for matching which are based on the strong assumption that all sources of extraneous variation among a case and its controls are accounted for [1,8,9]. A third program DESIGNM was written to compute such a formula (from , p.294), but DESIGNM does not adjust for a confounding variable, and that strong assumption of implicit matching is rarely justified in case-control studies, so this program was not made freely available. Software which compute sample sizes for conditional logistic regression, such as EGRET SIZ, are alternatives to DESIGNM, which is based on Miettinen's test of the Mantel-Haenszel odds ratio for matched case-control designs. The adjustment in DAYSMITH and DESIGN is for stratified matching [2,11,12], where matching is by confounders. This presumes that the eventual analysis will be unconditional  and will account for the stratification. Consequently, it is not required that F controls be linked with each case, only that the total number of controls be F times the total number of cases.
The literature [1,3,13,15] discusses stratified analysis interaction adjustment only for confounders with K = 2. It is easy, however, to modify the formulas for multi-level interaction. Every occurrence of RE in the formulas (Appendix 1) is replaced by RERIj, where RIj is the interaction factor corresponding to the jth level, j = 2,..., K. (For ?', put RIj inside the first sum.) We set RI1 = 1.
For two confounder levels, RI2, which is RI in Smith and Day's notation , is the multiplicative factor by which the odds ratio for those exposed and in level 2 of the confounder is different from the odds ratio when there is confounder-exposure-disease interaction. For RIj, contrast is between level j and the reference level (level one).
This adjustment was made available for sensitivity analysis; specifically, to explore how much the sample size result could change if the confounder were in fact an effect modifier. Nevertheless, the adjusted formulas have been used to determine sample size in the presence of gene-environment interaction .
The competitors to these programs are regression-based sample size programs, such as those in EGRET SIZ , which compute sample sizes required for unconditional logistic regression. The package nQuery  has an unconditional logistic regression option, but is not set up for case-control designs. These may be useful for continuous exposures, and make sense when the final analysis is intended to be such a regression, rather than a stratified analysis, such as a Mantel-Haenszel test, which our programs correspond to. We are unaware of any generally available competitor for stratified analysis.
In a series of papers on sample-size estimation to detect gene-environment interaction, which is a controversial role for sample-size formulas, comparisons have been made between regression based approaches and the stratified analysis approach [13,15]. One solution is even to consider a case-only design . EGRET SIZ provides no guidance for interaction adjustment, but it probably could be used for that purpose.
When there is more than one confounder, we define one super-confounder, where each category corresponds to a sub-category. For example, if age, with 5 categories, and smoking, with 2 categories, are both confounders, then we define one super-confounder with 10 = 5 ? 2 categories. The estimates of ri, pi, and RCi, i = 2, ...,10, then all have to take age and smoking into account jointly. As the number of confounders and the size of K increases, regression-based sample size programs become more advantageous, since information is not required for every sub-category.
The current programs yield results for 80% and 90% power, but versions are available for alternative powers, from 60% to 95%. A new version may print to the screen, if users want that option, and ask whether sample sizes for a specific power and Type I error are required.
The programs described are for two levels of disease (case vs. control) and of exposure. For several levels of exposure or disease, measures are available which correspond to odds ratios, risk ratios and risk differences , and it is not difficult to compute sample size formulas for these. If there is some demand, software to do those calculations may be created.
The Breslow-Day-Smith formulas which we extend utilize the classical method, based on testing. A more modern approach is that based on a confidence interval for the odds ratio , which may eventually become a program option. A Bayesian approach seems most suited for the sample size problem, although some issues need to be resolved . Although not yet written, a Bayesian solution will soon be formulated for case-control designs.
The pre-publication history for this paper can be accessed here:
Appendix 1 - Shows the formulas utilized by DESIGN and DAYSMITH. Appendix 2 - Shows output from the DESIGN session described in the main text.
The author is supported by an ?quipe grant from the FRSQ (Fonds de la recherche en sant? du Qu?bec). I appreciate the input of Eric Johnson, Sholom Wacholder and Jesse Berlin.
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