Skip to main content
NIHPA Author Manuscripts logoLink to NIHPA Author Manuscripts
. Author manuscript; available in PMC: 2020 Dec 1.
Published in final edited form as: Twin Res Hum Genet. 2019 Jul 29;22(6):757–760. doi: 10.1017/thg.2019.45

The NAS-NRC Twin Registry and Duke Twins Study of Memory in Aging: An Update

Margaret Gatz 1, Brenda L Plassman 2, Caroline M Tanner 3, Samuel M Goldman 4, Gary E Swan 5, Marianne Chanti-Ketterl 6, Ellen E Walters 7, David A Butler 8
PMCID: PMC7048234  NIHMSID: NIHMS1562423  PMID: 31354124

Abstract

The National Academy of Sciences-National Research Council (NAS-NRC) Twin Registry is one of the oldest, national population based-twin registries in the United States. It comprises 15,924 white male twin pairs born in the years 1917-1927, both of whom served in the armed forces, chiefly during World War II. This article updates activities in this registry since the most recent report in Twin Research and Human Genetics (Page, 2006). Records-based data include information from enlistment charts and Veterans Administration data linkages. There have been three major epidemiologic questionnaires and an education and earnings survey. Separate data collection efforts with the NAS-NRC registry include the National Heart, Lung, and Blood Institute (NHLBI) subsample, the Duke Twins Study of Memory in Aging, and a clinically-based study of Parkinson’s disease. Progress has been made on consolidating the various data holdings of the NAS-NRC Twin Registry. Data that had been available through the National Academy of Sciences are now freely available through National Archive of Computerized Data on Aging (NACDA).


The National Academy of Sciences-National Research Council (NAS-NRC) Twin Registry is a comprehensive registry of White male twin pairs born in the United States (US) between 1917 and 1927, both of the twins having served in the military, largely in World War II (WWII). The registry was created by the Medical Follow-Up Agency (MFUA), established shortly after WWII in response to a request by the US military to the National Academy of Sciences. MFUA personnel, led by Dr. Michael DeBakey, launched the registry in 1958-59 through obtaining birth certificates for White male multiple births from the years 1917-1927 from all states except Arizona, Connecticut, Delaware, Georgia, Maine, Missouri, Utah, Vermont, and the city of New Orleans, thus representing 93% of the US population at that time. Personnel matched birth certificates against Veterans Administration (VA) files to determine veteran status. These efforts led to identifying 15,924 pairs, or 31,848 individuals. These 31,848 individual twins constitute the NAS-NRC Twin Registry (Jablon et al., 1967).

As has been described in prior reports in this journal (Page, 2002, 2006), starting in 1965, the men were mailed a brief questionnaire (Q1) requesting their enrollment in the study and including questions to determine zygosity, with a baseline epidemiological assessment (Q2) mailed after the man replied to Q1. During this period, data were also abstracted for the entire registry from hard-copy military records, including branch, rank, dates of entry and separation, information from the induction physical, and--for a very small subsample-- either Army General Classification or Armed Forces Qualification Test scores. Three subsequent surveys gathered data via mailed questionnaire: a 1974 questionnaire (Q3) focused on education and earnings (Behrman et al., 1980) and epidemiological questionnaires in 1985 (Q7) and 1998 (Q8) that repeated and expanded on health questions in Q2. Questionnaire data were supplemented with medical records and disability data from the VA beginning with the years during which the man served and continuing through 1985, with the latest death update in 2012. A 2015 list of publications using NAS-NRC Twin Registry data includes 377 entries.

A number of separate data collection efforts engaged twins in the NAS-NRC Twin Registry from its beginnings. In 1969-72, funded by the National Heart, Lung, and Blood Institute (NHLBI), 514 twin pairs from the registry were recruited for clinical examination by virtue of living near Indianapolis IN, Framingham MA, or San Francisco, Davis, or Los Angeles CA. These pairs, called the NHLBI Twin Study (Feinleib et al., 1977), participated in up to six assessments, the most recent in 2002-03. Because the evaluations were in-person, they included cognitive testing, blood samples, and three waves of structural neuroimaging.

The Duke Twins Study sample, described by Plassman et al. (2006), comprised all NAS-NRC Registry twin pairs in which both twins were determined to be alive and residing in the US in 1989. For this purpose, Duke University investigators devoted considerable time to locating twins and updating contact information and vital statistics. There were four waves of data collection, each wave entailing multiple steps: The Telephone Interview for Cognitive Status, modified for epidemiological studies (TICS-m; Plassman et al., 1994) screened for cognitive impairment, with a proxy interview for those who could not complete a telephone interview. At each assessment wave, for individuals scoring below a cutoff on either TICS-m or the proxy interview, an informant was interviewed with the Dementia Questionnaire (DQ; Kawas et al., 1994) to determine whether to proceed to an in-person dementia evaluation. In-person assessments entailed comprehensive clinical evaluations, with the assembled information used to assign a consensus diagnosis as demented, cognitively impaired not demented, or cognitively normal; to apply standard criteria for Alzheimer’s disease (AD; McKhann et al., 1984) and other types of dementia; and to assign an age of onset for dementia.

The second telephone interview of all individual twins alive in 1992 included screening not only for dementia, but also for suspected parkinsonism (Tanner et al., 1999). Parkinsonism screening was repeated at the third wave of telephone interviewing from 1996-98. Those who screened positive and their twin brothers were invited to a study of Parkinson disease. Case ascertainment included an in-person neurological evaluation and a consensus diagnosis. Individuals were followed for a diagnosis of parkinsonism through 2015 using death certificates (Goldman et al., 2019).

The timeline for data collection and sample sizes are shown in Figure 1. Age ranges and zygosity are shown in Table 1. Note that all 15,924 pairs are shown in the table and figure, although some men never responded to any questionnaire or telephone invitation.

Figure 1.

Figure 1.

NAS-NRC Study Timeline

Table 1.

Sample sizes, age range, and zygosity

Total Registry
(at induction)
Baseline
(Q2)b
Q3 Q7 Q8
Number of respondents N = 31,848 N = 14,299 N = 4938 N = 9475 N = 6247
Age range 15 – 33 years 40 – 56 years 47 – 57 years 57 – 70 years 69 – 82 years
Zygositya
 MZ 37.5% 44.2% 53.3% 45.5% 46.9%
 DZ 47.6% 52.5% 472.% 49.5% 47.1%
 unknown 14.9% 3.3% 2.5% 5.0% 6.0%

Notes:

a.

Zygosity is based on DNA markers where available.

b.

We refer to the Qs by their original numbering by MFUA. Q2 constituted the baseline data collection. Induction data are available for 99% of all twins, whether or not they responded to any questionnaire or telephone data collection. Ns show how many men answered each wave.

Classification of zygosity in Q1 relied on responses to two questions: (i) ‘As children were you and your twin as alike as two peas in a pod or of only ordinary family resemblance?’; and ii) ‘In childhood, did parents, brothers and sisters or teachers have trouble in telling you apart?’ Agreement was 95% between questionnaire zygosity classification and blood typing results for 741 twin pairs (Hrubec et al., 1978). After DNA genotyping became available from twins seen in person, investigators found 96.8% agreement between DNA markers and questionnaire zygosity classification for 578 pairs (Reed et al., 2005). As DNA was not available in the majority of cases, a secondary classification of zygosity represents the twin pairs’ probability of being monozygotic, based on a logistic regression model that used existing DNA as the gold standard (Wu et al., 2010).

Notable Features of Registry

The NAS-NRC Twin Registry represents a unique slice of American history. The men in this registry are largely veterans of WW II—termed “The Greatest Generation” (Brokaw, 1998) to characterize their core values of personal responsibility, duty, and overcoming adversity. WWII involved the nation in a way not true of subsequent wars; thus, WWII veterans are representative of the white male population of the US of that era. Among all US males aged 45-49 in 1970, 71% were WW II veterans (Behrman et al., 1980). Also unique to these men was the “GI Bill” (formally, the Servicemen's Readjustment Act of 1944) that offered veterans tuition and expenses to attend college or vocational school, as well as low-interest home mortgages. The result was to make higher education available to the working class in a way heretofore unattainable. It is estimated that half of all WWII veterans participated in some educational or training program (National WWII Museum; U.S. Department of Veterans Affairs, 2013).

Updates Since Prior Reports

Whereas previously potential users of NAS-NRC Twin Registry data applied to the Twins Committee at the National Academy of Sciences and were assessed a user fee, NAS-NRC Twin Registry data are now available at no cost through the National Archive of Computerized Data on Aging (NACDA; Gatz & Butler, 2017). In addition, we have begun taking steps to consolidate the original NAS-NRC Twin Registry data (including military service records and Q1-Q8) with data collections that have taken place separately, especially the Duke Twins Study TICS-m and clinical diagnosis data. The NAS-NRC Twin Registry contributes data to larger consortia, including the CODATwins Project (Silventoinen et al., 2019) and the Consortium on Interplay of Genes and Environment across Multiple Studies (IGEMS; Pedersen et al., 2019). To stimulate data analyses and facilitate collaborations, the Twins Committee prepared a profile of the NAS-NRC cohort (Gatz et al., 2014).

In an example of collaboration across twin registries, Arden et al. (2016) used data from NAS-NRC Twin Registry; the Swedish Twin Registry; and the Danish Twin Registry to study the association between lifespan and intelligence. There was a small but statistically significant association between cognitive scores and age at death. Twin modelling established that the association was largely driven by genetic effects in all three samples. In other words, intelligence and lifespan are associated due to shared genes, potentially representing fundamental genetic fitness or some gene-environment correlation process where intelligence drives behaviors that promote longevity.

Another example of collaboration across twin registries is Amin et al.’s (2015) test of the effects of education on health. The authors included data from three US studies—the NAS-NRC Twin Registry, the Mid-Atlantic Registry, and the Minnesota Twin Registry. Using within monozygotic (MZ) twin pair estimators to identify causal relationships, they found small or non-significant associations between schooling and adult health. The finding suggests that associations between education and adult health in non-genetically informed studies may reflect unobserved genetic and social confounds.

Other recent publications are based on NAS-NRC twins data alone. Duke Twins data from four waves of telephone screening were analyzed by McArdle and Plassman (2009). They estimated heritability of episodic memory at the first wave to be 19% when including age and education as covariates. Longitudinal models found both additive genetic variance and unique environmental variance to increase with age. The Duke Twins telephone screening at waves 3 and 4 included a scale of Health Limitations of Personally Desired Activities (Gurland et al., 2015). Concordances for MZ and dizygotic (DZ) twins on the separate items were quite similar indicating that health-related limitations were largely influenced by unique environments. Median concordance at wave 3 was .07 for MZ and .08 for DZ. Median concordance at wave 4 was .11 for MZ and .09 for DZ (Gurland et al.). Wu et al. (2014) used Questionnaire 2 data, when the men were aged 45 to 55, to study self-reported alcohol use and hangover. They found 50% heritability for intoxication and 55% heritability for hangover. Shared environment played a minimal role.

A recent report estimated concordance and heritability for Parkinson’s disease (PD) in the NAS-NRC Twin Registry using results from in-person neurological evaluations during the 1990s in combination with National Death Index cause of death data through 2015 (Goldman et al., 2019). Among 220 pairs, probandwise concordance for PD was .20 in MZ and .13 in DZ pairs (heritability 27%). Genetic liability was much higher in pairs in which PD was diagnosed ≤ age 50 in the first affected twin (MZ concordance .75, DZ concordance .20, heritability 83%). Notably, concordance among DZ pairs was several-fold higher than has been reported for same sex non-twin siblings, suggesting substantial effects of shared intrauterine or childhood environment in PD etiology.

Other work with the registry is underway including a study on the long-term outcomes of traumatic brain injury; additional collaborative analyses through IGEMS and CODAT; and individual investigators’ studies using data accessed through NACDA.

Access to the Registry

Data are available at https://doi.org/10.3886/ICPSR36234.v5. Researchers are invited to download the “DS0 Study-Level Files” including the User Guide, which provide an extensive overview of data collection and phenotypes available, as well as the User Agreement, to complete and return to NACDA.

Acknowledgements

Funding for archiving the NAS-NRC Twin Registry data was provided by Grant No. R21 AG039572 from the National Institutes of Health. Assistance from Harriet Crawford and other staff at the National Academy of Sciences was crucial to the archiving task. Funding for the Duke Twins Study was provided by NIH Grant No. R01 AG008549.

Contributor Information

Margaret Gatz, Center for Economic and Social Research, University of Southern California, Los Angeles, CA 90089-3332, USA.

Brenda L. Plassman, Department of Psychiatry & Behavioral Sciences, Duke University School of Medicine, Durham, NC 27710, USA

Caroline M. Tanner, Department of Neurology, School of Medicine, University of California, San Francisco, San Francisco, CA 94122, USA

Samuel M. Goldman, Division of Occupational & Environmental Medicine, University of California, San Francisco, San Francisco, CA 94121, USA

Gary E. Swan, Stanford Prevention Research Center, Department of Medicine, Stanford University School of Medicine, Palo Alto, CA 94305, USA

Marianne Chanti-Ketterl, Department of Psychiatry & Behavioral Sciences, Duke University School of Medicine, Durham, NC 27710, USA.

Ellen E. Walters, Center for Economic and Social Research, University of Southern California, Los Angeles, CA 90089-3332, USA

David A. Butler, Office of Military and Veterans Health, Health and Medicine Division, The National Academies of Sciences, Engineering, and Medicine, Washington, DC 20001, USA

References

  1. Amin V, Behrman JR, & Kohler H-P (2015). Schooling has smaller or insignificant effects on adult health in the US than suggested by cross-sectional associations: New estimates using relatively large samples of identical twins. Social Science and Medicine, 127, 181–189. doi: 10.1016/j.socscimed.2014.07/065 [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Arden R, Luciano M, Deary IJ, Reynolds CA, Pedersen NL, Plassman BL … Visscher PM (2016). The association between intelligence and lifespan is mostly genetic, International Journal of Epidemiology, 45, 178–185. doi: / 10.1093/ije/dyv112 [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Behrman JR, Hrubec Z, Taubman P, & Wales TJ (1980). Socioeconomic Success. A Study of the Effects of Genetic Endowments, Family Environment, and Schooling. Amsterdam: North-Holland. [Google Scholar]
  4. Brokaw T (1998). The Greatest Generation. New York: Random House. [Google Scholar]
  5. Feinleib M, Garrison RJ, Fabsitz R, Christian JC, Hrubec Z, Borhani NO … Wagner JO (1977). The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results. American Journal of Epidemiology, 106, 284–295. [DOI] [PubMed] [Google Scholar]
  6. Gatz M & Butler D (2017-June-29). National Academy of Sciences-National Research Council Twin Registry (NAS-NRC Twin Registry), 1958-2013. Ann Arbor, MI: Inter-university Consortium for Political and Social Research. doi: 10.3886/ICPSR36234.v5 [DOI] [Google Scholar]
  7. Gatz M, Harris JR, Kaprio J, McGue M, Smith NL, Snieder H, Spiro A III, & Butler DA (2014) Cohort profile: The National Academy of Sciences-National Research Council Twin Registry (NAS-NRC Twin Registry). International Journal of Epidemiology, 44, 819–825. doi: 10.1093/ije/dyu181 [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Goldman SM, Marek K, Ottman R, Meng C, Comyns K, Chan P … Tanner CM (2019). Concordance for Parkinson's disease in twins: A 20-year update. Annals of Neurology, 85, 600–605. doi: 10.1002/ana.25441 [DOI] [PubMed] [Google Scholar]
  9. Gurland BJ, Page W, Small B, McArdle JJ, & Plassman BL (2015). Heritability of health and aging limitations on personally desired activities. Health Psychology Research, 3, 18–22. doi: 10.4081/hpr.2015.1981 [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hrubec Z & Neel JV (1978). The National Academy of Sciences-National Research Council Twin Registry: Ten years of operation In Nance WE (Ed.). Twin Research: Biology and Epidemiology. New York: Alan R Liss. [PubMed] [Google Scholar]
  11. Jablon S, Neel JV, Gershowitz H, & Atkinson GR (1967). The NAS-NRC Twin Panel: methods of construction of the panel, zygosity diagnosis, and proposed use. American Journal of Human Genetics, 19, 33–61. [PMC free article] [PubMed] [Google Scholar]
  12. Kawas C, Segal J, Stewart WF, Corrada M, & Thal LJ (1994). A validation study of the dementia questionnaire. Archives of Neurology, 51, 901–906. [DOI] [PubMed] [Google Scholar]
  13. McArdle JJ & Plassman BL (2009). A biometric latent curve analysis of memory decline in older men of the NAS-NRC Twin Registry. Behavior Genetics, 39, 472–495. doi: 10.1007/s10519-009-9272-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. McKhann G, Drachman D, Folstein M, Katzman R, Price D, & Stadlan EM (1984). Clinical diagnosis of Alzheimer’s disease: Report of the NINCDS/ADRDA Work Group under the auspices of the Department of Health and Human Services Task force on Alzheimer’s disease. Neurology, 34, 939–944. [DOI] [PubMed] [Google Scholar]
  15. National WWII Museum [n.d]. The GI Bill. Retrieved March 30, 2019, from https://www.nationalww2museum.org/students-teachers/student-resources/research-starters/research-starters-gi-bill
  16. Page WF (2002). The NAS-NRC Twin Registry of WWII military veteran twins. Twin Research, 5, 493–496. [DOI] [PubMed] [Google Scholar]
  17. Page WF (2006). Update on the NAS-NRC Twin Registry. Twin Research & Human Genetics, 9, 985–987. [DOI] [PubMed] [Google Scholar]
  18. Pedersen NL, Gatz M, Finch BK, Finkel D, Butler DA, Dahl Aslan A, Franz CE, Kaprio J, Lapham S, McGue M, Mosing MA, Neiderhiser J, Nygaard M, Panizzon M, Prescott CA, Reynolds CA, Sachdev P, & Whitfield KE (2019). IGEMS: The Consortium on Interplay of Genes and Environment Across Multiple Studies — An Update. Twin Research and Human Genetics. 10.1017/thg.2019.76 [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Plassman BL, Newman TT, Welsh KA, Helms M, & Breitner JCS (1994). Properties of the Telephone Interview for Cognitive Status. Application in epidemiological and longitudinal studies. Neuropsychiatry, Neuropsychology, and Behavioral Neurology, 7, 235–241. [Google Scholar]
  20. Plassman BL, Steffens DC, Burke JR, Welsh-Bohmer KA, Newman TN, Drosdick D … Breitner JCS (2006). Duke Twins Study of Memory in Aging in the NAS-NRC Twin Registry. Twin Research & Human Genetics, 9, 950–957. [DOI] [PubMed] [Google Scholar]
  21. Reed T, Plassman BL, Tanner CM, Dick DM, Rinehart SA, & Nichols WC (2005). Verification of self-report of zygosity determined via DNA testing in a subset of the NAS-NRC Twin Registry 40 years later. Twin Research & Human Genetics, 8, 362–367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Silventoinen K, Jelenkovic A, Yokoyama Y, Sund R, Sugawara M, Tanaka M, … Kaprio J (n.d.). The CODATwins Project: The Current Status and Recent Findings of Collaborative Project of Development of Anthropometrical Measures in Twins. Twin Research and Human Genetics. 10.1017/thg.2019.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Tanner CM, Ottman R, Goldman SM, Ellenberg J, Chan P, Mayeux R, & Langston JW (1999). Parkinson disease in twins: An etiologic study. JAMA, 281, 341–346. [DOI] [PubMed] [Google Scholar]
  24. U.S. Department of Veterans Affairs (2013, November 21). Education and Training. History and Timeline. Retrieved March 30, 2019, from https://www.benefits.va.gov/gibill/history.asp
  25. Wu S-H, Guo Q, Viken RJ, Reed T, & Dai J (2014). Heritability of usual alcohol intoxication and hangover in male twins: The NAS-NRC Twin Registry. Alcoholism: Clinical and Experimental Research, 38, 2307–2313. doi: 10.1111/acer.12487 [DOI] [PubMed] [Google Scholar]
  26. Wu T, Page WF, & Snieder H (2010). Genetic and environmental influences on blood pressure and body mass index in the NAS-NRC World War II Veteran Twin Registry. [Abstract]. Twin Research & Human Genetics, 13, 293. [Google Scholar]

RESOURCES