Social Science & Medicine 66 (2008) 1675e1677
Arguments prove nothing unless verified. A commentary on
Kaufman’s ‘‘Epidemiologic analysis of racial/ethnic disparities:
Some fundamental issues and a cautionary example’’
a 3330 Hospital Drive NW, Room G208, Calgary, AB, Canada T2N 4N1
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Keywords: Therapeutic efficacy; Heart failure; Study design; Race; ACE inhibitors
‘‘The strongest arguments prove nothing so long as
‘‘Studies of Left Ventricular Dysfunction’’ (SOLVD)
the conclusions are not verified by experience. Ex-
data was not an attempt to replicate a randomized con-
perimental science is the queen of sciences and
trolled trial but to improve, albeit with remaining in-
equalities, our ability to identify potential reasons forpreviously reported differences in outcome
Roger Bacon (1214e1294), philosopher and advo-
). Our analysis was never suggested to be
more than hypothesis generating. The over-interpreta-
Jay Kaufman has attempted to provide a scholarly
tion by Kaufman and others served their purposes,
assessment of pitfalls in attempting to assign the cause
not ours. In addition, his criticisms of our analytic ap-
of disease outcomes to apparent racial differences
Our statements in the New England Journal of Med-
in his arguments, he has continued to follow the same
icine article were intentionally worded to discourage
path as other authors, whom he appears to deride, in
mis-interpretation or over-interpretation of our findings.
misinterpreting the conclusions of our 2001 paper,
Since prior heart failure trials were conducted predom-
‘‘Lesser response to angiotensin-converting-enzyme in-
inantly in white subjects and possible differences of re-
hibitor therapy in black as compared with white patients
sponse in blacks were uncovered it was correct to state
with left ventricular dysfunction’’ published in the New
that ‘‘the overall population of black patients with heart
failure may be underserved by current therapeutic rec-
ommendations’’ and ‘‘it seems appropriate to consider
Despite Kaufman’s assertions, the matched-cohort
current therapeutic recommendations as applying to
design we used in our retrospective analysis of
white patients but not necessarily to black patients’’. These comments are clearly in the context of a hypothe-sis, not a definitive conclusion. Our recommendation for
* Corresponding author. Tel.: þ1 403 220 3219; fax: þ1 403 210
‘‘clinical trials in black patients that are designed pro-
spectively to evaluate therapeutic responses.’’ (
0277-9536/$ - see front matter Ó 2007 Elsevier Ltd. All rights reserved. doi:10.1016/j.socscimed.2007.11.049
D.V. Exner, J.N. Cohn / Social Science & Medicine 66 (2008) 1675e1677
p. 1357) further emphasized our recognition
responsible for the differences in outcome that were ob-
for the need of additional, prospective randomized data.
served between the two groups. The abstract to our pa-
We recognize that our matched-cohort design, as
per specified ‘‘no significant change in the risk of death
with any study of this kind, was imperfect. Yet, many
was observed in association with enalapril therapy in ei-
of Kaufman’s criticisms are unmerited. Our matching
strategy was described as ‘‘questionable because race
were further highlighted in Table 3 of our paper and
specific comments were made that ‘‘mortality was sim-
method used was both appropriate and scientifically
ilar among the black patients and the matched white pa-
valid. The comment that ‘‘once the data are already col-
tients regardless of treatment assignment’’ and that ‘‘no
lected, however, one can’t generally do better by throw-
significant alteration in mortality was observed in asso-
ing away a large proportion of these data’’ (
ciation with enalapril therapy’’ ).
is erroneous. In fact, a paper used to support
Thus, it is neither surprising nor unexpected that subse-
Kaufman’s criticisms states that ‘‘matching can be ex-
pected to increase efficiency’’ when both the matching
variables, and exposure, self-identified race, are nega-
The analysis we reported in 2001 never attempted to
That was the situation for our analysis.
identify genetic or environmental factors that might
Despite Kaufman’s assertions related to our statistical
contribute to our observations. Studies demonstrating
models, we were cognizant of issues related to residual
lesser antihypertensive potency of ACE inhibitors in
confounding and misclassification and used great care
black than in white hypertensive patients (
to deal with these issues as best we could. We acknowl-
also have made no such attempt. On two points
edged these limitations in our paper by stating that ‘‘no
we agree with Kaufman. The findings from our paper
degree of statistical adjustment can ensure complete
have been both over-interpreted and mis-interpreted
comparability’’ (, p. 1357). Further,
by others. Our analysis was conducted to investigate
the comment that ‘‘it is well appreciated in the theoret-
whether observed differences in outcome could, in
ical epidemiologic literature that groups with higher
part, be explained by differences in therapeutic re-
baseline risk will in general have more modest response
sponse. If confirmed, we planned to conduct additional,
definitive research in this area aimed at improving the
lives of patients with heart failure. This research has
theoretical concept is not universally accepted (
been completed. We also agree that a ‘‘randomized
Moreover, it is well known that patients with left
controlled trial (RCT) is widely considered to be
ventricular systolic dysfunction and a higher baseline
the gold standard for establishment of causality in
risk derive greater benefit from therapeutic interven-
tions, in terms of absolute benefit, than do patients
been followed by at least one prospective randomized
trial designed to address therapeutic response in
a self-identified black population with heart failure
It is clear that a therapeutic reduction of hospitaliza-
tion rate is a particularly sensitive guide to efficacy in
apy that reduces mortality, reduces hospitalization, and
sicker patients, as evidenced by its usefulness in recent
enhances quality of life in these patients. Such data are
studies in advanced Classes III and IV heart failure
critical both in providing valid evidence and in assisting
physicians in treating individual patients.
tality as a guide to severity of heart failure, even thoughdifferences in mortality, comparing white and black pa-
tients, may be a result of health management disparities. Furthermore, Kaufman claims that in our paper ‘‘the
Cohn, J. N., Julius, S., Neutel, J., Weber, M., Turlapaty, P., & Shen, Y.,
null finding for mortality is largely ignored.’’ (
et al. (2004). Clinical experience with perindopril in African-
In doing so he fails to appreciate that in
American hypertensive patients: a large United States community
the SOLVD Prevention Trial, which was the source of
trial. American Journal of Hypertension, 17, 134e138.
most of our black patients, mortality was not reduced
Dawid, A. P. (2002). Counterfactuals: help or hindrance? Interna-
tional Journal of Epidemiology, 31(2), 429
). We also clearly reported that differences
Dries, D. L., Exner, D. V., Gersh, B. J., Cooper, H. A., Carson, P. E.,
in rates of hospitalization for heart failure were
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& Krum, H., et al. Carvedilol Prospective Randomized Cumula-
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vedilol on the morbidity of patients with severe chronic heart
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Gasz Balázs, Benkő László, Jancsó Gábor, Lantos János, Alotti Nasri, Rőth ErzsébetOxidatív stressz és gyulladásos válaszreakciók mértékének vizsgálata hagyományos és pumpa nélküli koronáriaműtétekbenCard. Hung. 2003, 33 (Suppl. 2): A55. Alotti Nasri, Simon József, Kassai Imre, Tarsoly László, Csordás József, Harang PéterÉrdemes-e végezni carotis és szívműtétet
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