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9
Analysis Structure
OVERVIEW
The analysis plan for the Five Series Study was structured to check data va-
lidity, test hypotheses, and interactively explore data to follow leads arising
from data analysis. The study was designed to address whether
. participation in at least one of the five selected atmospheric nuclear
weapons tests is associated with increased mortality hazard; and
. participants who were more likely to have been highly exposed to radia-
tion would have increased mortality hazard relative to participants who were
less likely to have been highly exposed.
The basic comparison involves the survival experience of participants rela-
tive to that of referent cohort members. Because various diseases have different
degrees of radiogenicity (Mettler and Upton, 1995), hazard ratios have been
calculated for mortality from all causes, all malignancies, and leukemia (ex-
cluding chronic lymphocytic leukemia). Other radiogenic cancers, along with a
selection of presumed nonradiogenic diseases and conditions, are also examined.
Disease categories were discussed and defined, using International Classifica-
tiorl of Diseases, 9th Edition, codes, before analysis began (see below).
AVAILABLE DATA
Data available for the analysis of survival times consist of measures or indi-
cators of (1) presumed radiation exposure, (2) individual and military service
characteristics that might confound an association between exposure and out-
come, and (3) mortality outcome. Table 9-1 presents the variables that were in-
cluded in the analysis dataset. It should be noted that variables were not all of
the same quality with regard to completeness and validity.
50
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ANALYSIS STRUCTURE
TABLE 9-1. Variables Considered for Analysis and Their Utility
Variable
Example
Utility
Participant status
Sex
Paygrade
Branch of service
Selection series
Date of selection seriesb
Location
Shot
Number of series
Number of shots
Unit category
Unit of assignment
Rank/rating
Occupation
Tasks during test
Dose
Device
Date of birth
Vital status
Date of death
Age at selection series
Years since atomic test
exposured
Age at death or censured
Calendar decade of deaths
Decade since selection
· d
series
Underlying cause of death
Associated causes of
death
Participant
Male
E3
Air Force, Army, Marines, Navy
CASTLE
April 1, 1953
Pacific
BRAVO
3
12
Technical
9740 TSU Chemical Section
Private, PVT2
E.g., pilot, navigator
Cloud sampler pilot
2.4 rem
Thermonuclear
January 15, 1923
Dead
March 7, 1972
Date of selection series minus
date of birth
Date of death or censoring minus
date of selection series
Date of death or censoring minus
date of birth
1960s
20-30 years since shot
+e
+d,e
+1
e
l
e
+/_e
+/_e
Malignant neoplasm of the lung +
Hypertensive heart disease
+
aPlus or minus assigned based on general consideration of validity and
completeness; a plus indicates that data are available and of good quality; a
minus indicates that data are either unavailable or of poor quality.
bThe first day of the operational period of the selection series.
CCategories created and assigned based on unit of assignment.
Value calculated from specified dates in dataset.
equality of fact and date data is discussed in this report. For known deaths,
the quality is excellent; the Department of Veterans Affairs data system may
not have ascertained all deaths of study cohort members.
51
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52
THE FIVE SERIES SI UDY
ANALYSIS
Variables
The variables included in the basic analyses are participant status, age at
selection series, paygrade, branch of service, and selection series. Analyses also
explore relationships using variables such as land versus sea series; age-calen-
dar time; disease latency; series and post-series time periods; number of series;
and associated causes of death. (The definitions and rationale for the use of these
variables are described elsewhere in this report.)
To appropriately test the second question whether a dose-response rela-
tionship exists between radiation exposure and mortality hazard an at-least-
ordinal variable that ranks an exposure surrogate measure would be needed.
(Note: A working group of the committee overseeing the Five Series Study has
reported kIOM, 1995; reprinted in Appendix A of this report] that the extensive
dosimetry categorization and reconstruction data developed by the Nuclear Test
Personnel Review Program of the Defense Threat Reduction Agency are not
suitable for use in epidemiologic investigations of dose-response. This analysis
plan does not, therefore, use the dosimetry data as exposure variables in the sta-
tistical analysis.) These surrogates could incorporate information from military
records, eyewitness accounts, and historical records known about groups more
and less likely to have received higher radiation doses. Using the exposure sur-
rogates, statistical models could test for these proxy dose-response relation-
ships. (See Chapter 7.)
Type of Analysis
The research group defined two analytic approaches. The first uses standard-
ized mortality ratios (SMRs), calculated for each cohort (participant and referent)
separately using standard rates adjusted for age and time distributions (Marsh et
al., 1998; Rothman and Greenland, 1998.~. The second involves proportional haz-
ards modeling using the wider range of available covariates (Allison, 1995~.
SMRs are a commonly used tool to compare death rates among a cohort of
interest to those in a larger, reference population, customarily the U.S. general
population. The deaths that actually occur in the cohort of interest are labeled
"observed" deaths; one also calculates the "expected" number of deaths that
would have occurred had the members of the cohort died at the same rate as the
U.S. population with the same age, race, and sex distribution. The ratio of ob-
served to expected deaths is an SMR, which is equal to 1.0 if the number of
The organizational locus of the Nuclear Test Personnel Review Program within the
Department of Defense has been the Defense Nuclear Agency (until June 1996), the De-
fense Special Weapons Agency (until October 1998), and, currently, the Defense Threat
Reduction Agency.
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ANALYSIS STRUCTURE
53
deaths observed in the cohort of interest is the same as the number of deaths
expected to have occurred if the cohort members had died at U.S. population
death rates.
Sex and race information was not included in the datasets for this study. For
the 61.7 percent of deaths for which we were able to acquire death certificates,
race and sex information is available. Less than half a percent (0.4%) of the
death certificates were coded as female; between 8 and 9 percent as black. These
proportions may not accurately reflect the unknown percentages of male and
black members of the participant and referent cohorts. Because both race and
sex are associated with mortality (both survival time and cause of death), they
do not provide valid estimates of the full at-risk cohort. We used white male
population rates for SMR calculations.
SMRs thus show whether the mortality of the cohort of interest is higher or
lower than that of the U.S. population. One typically sees SMRs for veterans
cohorts that are less than 1.0. Reasons given focus on the requirement that mili-
tary servicemen pass an entrance physical and also pass periodic physical fitness
exams while in military service, both effectively screening in favor of healthier
individuals versus their general civilian counterparts. Not only is this healthiness
thought to produce lower death rates among active duty military personnel, but
lower mortality rates apparently persist even after discharge from active duty
(Seltzer and Jablon, 1974, 1977~. Such effects seen among occupational groups
have been labeled the "healthy worker effect," and by analogy, lower SMRs
among military veterans can be attributed to a "healthy soldier effect." Despite
this limitation, SMRs provide a way to compare the mortality of the cohort of
interest to that of the general population. Also, because SMRs are based on
standard distributions of deaths, they can be compared across studies. We used
OCMAP Plus software to compute SMRs (Marsh et al., 1998~.
Cox proportional hazard ratio analysis (Cox, 1972) is used for the core
analyses in this report. We implemented these analyses using the SAS program
PHREG (SAS Institute, 1996~. In this approach, the risk of death in statistical
terms, the hazard is modeled in a regression that includes a baseline hazard as
well as coefficients that represent the additional hazards associated with various
factors such as in this case nuclear test series participation. The coefficient
associated with a factor represents a hazard ratio, which can be interpreted as a
relative risk of death that remains constant over the follow-up period. In our
analyses, coefficients were included for test series participation, age at time of
first participation, and age at time of first participation squared and cubed. Haz-
ard ratios are considered statistically significant if their associated 95 percent
confidence interval excludes the value 1.0. The time scale for these models was
attained age, which is thought to be the most appropriate scale for the kinds of
analyses we undertook (Korn et al., 19974.
Rather than fashion regression models that included risk estimates for other
factors such as test series, branch of service, and paygrade, we chose to include
these as stratification variables. Although this choice does not permit the esti-
mation of risks associated with the stratification variables, it does allow more
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54
THE FIVE SERIES SILLY
complete control of the effects of these variables (see Allison t1995] for further
detail). Finally, if we did not have definitive evidence of death for an individual,
he was considered to be not known dead (alive); if the individual was thought to
be dead, but there was no date of death or date of birth (there were only 38 of
these), this record was excluded from the analyses.
Diagnosis Groups
Based on tables from other studies of atomic veterans (e.g., Pearce et al.,
1997) yet expanded, the staff and committee chose which categories of diagno-
sis codes to examine: (1) the broad categories of noncancer causes of death; (2)
all malignant neoplasms; and (3) focused groups of malignancies, including leu-
kemias and other putatively radiogenic malignancies. Tables 9-2 and 9-3 present
the cause-of-death categories considered in this report.
TABLE 9-2. Broad Categories of Noncancer Causes of Death
as Grouped by ICD-9 Codes
Broad Category
ICD-9 Code
Infectious and parasitic diseases
Benign neoplasms
Endocrine, nutritional, and metabolic diseases
and immunity disorders
Diseases of the blood and blood-forming organs
Mental disorders
Diseases of the nervous system and sense organs
Circulatory disease
Respiratory disease
Digestive disease
Diseases of the genitourinary system
Diseases of the skin and subcutaneous tissue
Diseases of the musculoskeletal system and
connective tissue
Congenital anomalies
Symptoms, signs, and ill-defined conditions
All external causes
*
Total
001-139
210-239
240 279
280-289
290-319
320-389
390~59
460-519
520-579
580~29
680-709
710-739
740-759
780-799
800-999
001-139, 210-999
Not included are complications of pregnancy, childbirth, and the puer-
perium, and certain conditions originating in the perinatal period.
SOURCE: International Classification of Diseases, 9th Edition (ICD-9)
(USDHHS, 1991~.
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ANALYSIS STRUCTURE
TABLE 9-3. Cause-of-Death Categories Within Broad
Category of Malignant Neoplasms
Site ICD-9 Code
Lip, oral cavity, and pharynx
Digestive organs and peritoneum
Esophagus
Stomach
Small intestine
Colon
Rectum
Liver and intrahepatic bile ducts
Gallbladder
Pancreas
Respiratory and intrathoracic organs
Nasal
Larynx
Lung
Bone, connective tissue, skin, and breast
Bone
Connective tissue
Skin
Skin nonmelanoma
Breast
Genitourinary organs
Prostate
Testis
Bladder
Kidney
Other
Brain and nervous system
Thyroid
Other solid cancer
Total hematological
Non-Hodgkin's lymphoma
Hodgkin's disease
Multiple myeloma
Leukemia
Leukemia, excluding chronic lymphoid leukemia
Total
140 149
150
151
152
153
154
155
156
157
160
161
162
170
171
172
173
185
186
188
189
191, 192
193
14~199
20~208
200, 202
201
203
20~208
204.0, 204.2-208.9
14~208
Not listed separately are malignant neoplasms of the retroperitoneum and
peritoneum; other digestive organs; pleura; thymus, heart, and mediasti-
num; other respiratory and intrathoracic organs; female breast; female
genital organs; penis and other male genital organs; eye; other (than thy-
roid) endocrine glands; other, ill-defined, secondary, and unspecified sites.
SOURCE: International Classification of Diseases, 9th Edition (ICD-9)
(USDHHS, 1991).
55
Representative terms from entire chapter:
five series