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Diabetes Care 29:560-565, 2006
DOI: 10.2337/diacare.29.03.06.dc05-1901
© 2006 by the American Diabetes Association
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Pathophysiology/Complications
Original Article

Diabetes and Function in Different Cognitive Systems in Older Individuals Without Dementia

Zoe Arvanitakis, MD1,2, Robert Smith Wilson, PHD1,2,3, Yan Li, PHD4,5, Neelum Thanik Aggarwal, MD1,2 and David Alan Bennett, MD1,2

1 Rush Alzheimer’s Disease Center, Rush University Medical Center, Chicago, Illinois
2 Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois
3 Department of Behavioral Sciences, Rush University Medical Center, Chicago, Illinois
4 Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois
5 Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois

Address correspondencereprint requests to Zoe Arvanitakis, MD, Rush Alzheimer’s Disease Center, Rush University Medical Center, 600 South Paulina St., Suite 1020, Chicago, IL 60612. E-mail: zoe_arvanitakis{at}rush.edu


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
OBJECTIVE—To examine the relation of type 2 diabetes to the level of function in five different cognitive systems in older individuals without dementia.

RESEARCH DESIGN AND METHODS—Participants were 882 older men and women without dementia participating in the Rush Memory and Aging Project, a longitudinal clinical-pathological study of aging and dementia. They underwent uniform evaluations, which included clinical classification of dementia, and detailed cognitive function testing from which previously established summary measures of episodic memory, semantic memory, working memory, perceptual speed, visuospatial ability, and global cognition were derived. Diabetes was identified by history and direct medication inspection.

RESULTS—Diabetes was present in 116 (13%) participants. In separate linear regression models controlling for age, sex, and education, diabetes was associated with lower levels of semantic memory (P < 0.001) and perceptual speed (P = 0.005), but not with episodic memory, working memory, or visuospatial ability or with a measure of global cognition. The associations of diabetes with cognition were reduced when controlling for several vascular variables, and the associations were substantially stronger in current smokers than in individuals who never smoked or formerly smoked.

CONCLUSIONS—These results suggest that type 2 diabetes is associated with cognitive impairment, especially in semantic memory and perceptual speed and that these effects may be modified by smoking status.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 
Type 2 diabetes is a common disease in older age, affecting about one in five individuals over the age of 65 years. It is associated with mortality and significant morbidity, including neurological disability. Although the effects of diabetes on the peripheral nervous system are well established, the effects of diabetes on the central nervous system have been less clear (1,2). Several studies have found that diabetes is related to dementia (3,4) and lower levels of cognitive function (5,6), whereas others have not (7,8). Further, some studies found that diabetes was associated with lower scores on some individual cognitive tests, but not on others (9,10), suggesting that diabetes may differentially affect cognition. To date, few studies have systematically examined the relation of diabetes to different cognitive domains in a large cohort of older individuals (11). Further, to our knowledge, none have identified factors that might modify this relation.

We used data from the Rush Memory and Aging Project, an ongoing epidemiologic study of neurological conditions of old age, to examine the relation of diabetes to cognitive function in nearly 900 older individuals free of dementia. We examined the relation of type 2 diabetes to summary measures of specific cognitive domains and of global cognitive function. In addition, because of the relation of diabetes to vascular disease, we examined whether selected vascular risk factors, such as smoking, or conditions, such as stroke, could explain or modify the relation of diabetes to cognition.


   RESEARCH DESIGN AND METHODS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
RESULTS
 CONCLUSIONS
 References
 
All participants were older individuals who enrolled in the Rush Memory and Aging Project, an ongoing longitudinal clinical-pathological study of risk factors for chronic neurological conditions of old age (12,13). They were recruited from retirement facilities in the greater Chicago metropolitan area, and all provided informed consent. The study was approved by the Institutional Review Board of Rush University Medical Center.

Individuals were eligible for these analyses if they had completed a baseline clinical evaluation and were free of dementia. Clinical evaluations were structured and uniform and included a medical history, neurological examination, and a detailed assessment of cognitive function (see below). All participants were asked to bring prescription and over-the-counter medication containers, which were then visually inspected and coded using the Medi-Span system (14). Each participant was examined by a neurologist or geriatrician experienced in the evaluation of individuals with dementia who, after review of all clinical data, classified participants with respect to dementia (15). Of the 941 individuals enrolled in the study from 1 January 1997 to 1 April 2005, 59 met criteria for dementia and were excluded from analyses. In the remaining 882 individuals, age was 80.5 ± 6.9 years (mean ± SD), education was 14.4 ± 3.1 years, and the Mini-Mental State Examination score was 27.8 ± 2.2; 73.5% were women and 91.2% were white and non-Hispanic.

Assessment of diabetes
Diabetes was present if, at the baseline evaluation, the participant reported a history of diagnosis of diabetes or was taking medication (insulin or oral hypoglycemic) to treat diabetes, as determined by direct inspection of all prescription and nonprescription medication containers. A history of diabetes was identified by answering "yes" to any of three questions: 1) "Have you ever been told by a doctor, nurse, or therapist that you had diabetes, or sugar in the urine, or high blood glucose?" 2) "Has a doctor, nurse, or therapist ever told you to take insulin or injections for your high blood glucose?" 3) "Has a doctor, nurse, or therapist ever told you to take medicine by mouth for your high blood glucose?" The identification of diabetes is consistent with that previously reported in the Religious Orders Study (2,11).

Assessment of cognitive function
Cognitive function tests were selected to assess a broad range of cognitive abilities commonly affected by aging (16). The Mini-Mental State Examination was used for descriptive purposes but not in analyses. The remaining 19 tests were chosen to assess five cognitive domains that may be differentially related to a variety of diseases or conditions. The grouping of tests into the five cognitive domains was supported by a factor analysis with varimax rotation (16). The agreement between the factor analytic grouping and the hypothesized grouping was assessed with the Rand’s statistic, which equaled 0.79, indicating a good fit (P < 0.001 for the hypothesis test of no concordance). Episodic memory was evaluated using seven tests: Word List Memory, Word List Recall, and Word List Recognition from the procedures established by the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) (17); immediate and delayed recall of Story A from the Logical Memory subtest of the Wechsler Memory Scale–Revised (18); and immediate and delayed recall of the East Boston Story (19). Three tests assessed semantic memory: Verbal Fluency (17), an abbreviated version of the Boston Naming Test (17), and an abbreviated version of the Reading Test (20). There were three working memory tests: Digit Span Forward and Backward of the Wechsler Memory Scale–Revised (18) and Digit Ordering (21). Four tests assessed perceptual speed: the Symbol Digit Modalities Test (22), Number Comparison (23), and two indexes from a modified version of the Stroop Neuropsychological Test (16). Visuospatial ability was evaluated by two tests: items from Judgment of Line Orientation and Standard Progressive Matrices (24).

To minimize floor and ceiling effects and other sources of measurement error, we constructed summary measures of each cognitive domain for use in analyses, rather than using individual test scores. We used previously established summary measures (16) of five cognitive domains, episodic memory, semantic memory, working memory, perceptual speed, and visuospatial ability, as well as a summary measure of global cognitive function. Each cognitive domain summary measure was derived by converting the raw scores from the corresponding individual tests to z scores, using the mean and SD from the evaluation of all participants in the study and averaging the z scores. A measure of global cognitive function was formed by averaging the z scores of all 19 tests. Valid summary measures required valid scores on at least half of the component tests, which was the case for >98% of participants for each of the six summary measures.

Assessment of vascular risk factors and conditions
A comprehensive baseline medical history is collected on all participants in the Rush Memory and Aging Project. A variety of questions pertain to vascular risk factors, including current and former smoking, and vascular conditions, including a history of stroke, myocardial infarction, congestive heart failure, and claudication. Current smoking was based on the question, "Do you smoke cigarettes now?" and, if the participant answered "no," then he or she was asked about former smoking based on the question, "Did you ever smoke cigarettes regularly?" Questions pertaining to leg claudication were derived from the Rose questionnaire (25). Further, clinical examinations allowed for documentation of several health and disease indexes. Systolic blood pressure was obtained from the average of three measures of systolic pressure (two while sitting and one after standing 1 min), and diastolic blood pressure was similarly obtained. Other indexes collected during the examinations included measured height and weight to calculate BMI (kg/m2), as well as signs suggestive of stroke on neurological examination. These signs included a unilateral pronator drift, focal weakness, asymmetric reflexes, and a Babinski sign. For the purpose of this study, current or former cigarette smoking history, myocardial infarction, congestive heart failure, and claudication were rated as absent or present as determined by self-report. Systolic and diastolic blood pressure and BMI were based on the examinations and were analyzed as continuous variables. Stroke was the examining physician’s diagnosis based on the clinical history and neurological examination findings.

Data analyses
The relation of diabetes to cognitive function was examined in a series of linear regression models. All models were adjusted for age, sex, and education. We first examined the relation of diabetes to each measure of function in a specific cognitive domain and then to a measure of overall cognitive ability. Because there were six outcomes, we used a P value of 0.008 (0.05 divided by 6) for a two-sided test as a cutoff score for significance for all regression analyses presented here. In subsequent analyses of cognition, we repeated the core models with terms added separately for nine vascular risk factors or conditions that might account for the association of diabetes with cognition. We then tested in separate models whether any of these nine vascular variables modified the relation of diabetes to cognition. Finally, after identifying an interaction between diabetes and smoking, we examined the effect of three separate model terms (no diabetes, smoking; diabetes, no smoking; diabetes, smoking) on each of the six cognitive outcome measures. Models were validated graphically and analytically. Programming was done in SAS.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
CONCLUSIONS
 References
 
Characteristics of individuals with and without diabetes
Of the 882 study participants included in these analyses, diabetes was present in 116 (13%). Of those with diabetes, 77 (66%) were taking medication for the treatment of diabetes: 9 were taking insulin but no oral hypoglycemic drug, 57 were taking an oral hypoglycemic drug but no insulin, and 11 were taking both. Overall, individuals with diabetes were younger, more likely to be men, less educated, more likely to have a history of congestive heart failure, and more likely to have an elevated BMI (Table 1).


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  		Table 1— Characteristics of 882 participants according to the presence or absence of diabetes

 
Diabetes and cognitive function
We first examined the relation of diabetes to each of the five cognitive domains in separate linear regression models that adjusted for age, sex, and education (Table 2). Diabetes was associated with lower performance in two cognitive domains: diabetes was associated with a 0.206 lower score on the measure of semantic memory and with a 0.228 lower score on the measure of perceptual speed. The effect of diabetes on semantic memory or on perceptual speed was equivalent to the effect of ~14 and 6 years of age, respectively. Diabetes was not associated with episodic memory, working memory, or visuospatial ability.


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  		Table 2— Relation of diabetes to cognitive function in five different cognitive domains and to global cognition

 
Because of the finding of associations of diabetes and two cognitive domains, we next examined whether diabetes was related to the composite measure of global cognitive ability. We did not find a significant association, although the effect of diabetes on global cognition was in the expected direction (Table 2).

Factors that might account for the association of diabetes with cognition
We next considered the possibility that vascular risk factors or conditions might account for the relation of diabetes to semantic memory and perceptual speed.

In separate analyses, we added terms for nine vascular variables. The association of diabetes with semantic memory was unchanged in analyses that controlled for stroke, systolic blood pressure, diastolic blood pressure, myocardial infarction, claudication, former smoking, or current smoking. By contrast, after controlling for congestive heart failure (estimated coefficient –0.171; SE = 0.067, P = 0.011) or BMI (estimated coefficient –0.147; SE = 0.061, P = 0.017), the relation of diabetes to semantic memory was no longer significant.

The association of diabetes with perceptual speed was unchanged in analyses that controlled for stroke, myocardial infarction, claudication, or former smoking. However, the association was no longer significant when controlling for congestive heart failure (estimated coefficient –0.184; SE = 0.089, P = 0.039), BMI (estimated coefficient –0.158; SE = 0.083, P = 0.058), current smoking (estimated coefficient –0.190; SE = 0.080, P = 0.018), systolic blood pressure (estimated coefficient –0.209; SE = 0.080, P = 0.009), or diastolic blood pressure (estimated coefficient –0.204; SE = 0.080, P = 0.011).

Potential modifiers of the association of diabetes with cognition
In subsequent analyses, we tested whether each of the same vascular risk factors and conditions modified the relation of diabetes to any of the five cognitive systems or to global cognition by adding terms for the interaction of diabetes with each covariate in separate models.

There were no interactions between diabetes and any of the vascular variables, except for with current smoking. There were 34 current smokers, of whom 7 had diabetes (Table 1). We conducted separate analyses using the five cognitive domains as outcome measures to explore whether the interaction of diabetes and current smoking affected level of function in different cognitive domains (Table 3). Compared with a reference group of individuals without diabetes and who do not smoke, individuals with diabetes who smoke had significantly lower levels of semantic memory, working memory, and perceptual speed. Individuals without diabetes who smoke or those with diabetes who did not smoke did not have lower levels of function in these three cognitive domains. There was no significant interaction of diabetes and current smoking on episodic memory or visuospatial ability.


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  		Table 3— Relation of diabetes to cognition as a function of current smoking status

 
Similarly, compared with a reference group of individuals without diabetes and who do not smoke, individuals with diabetes who smoke had a significantly lower level of global cognition, whereas individuals without diabetes who smoke or those with diabetes who did not smoke did not have a lower level of function (Table 3).


   CONCLUSIONS
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
References
 
In this study of nearly 900 older individuals free of dementia, we found that diabetes was associated with cognitive impairment. Diabetes was related to some cognitive domains, particularly semantic memory and perceptual speed, but not others. Consistent with a previous study (26), we found that the effect of diabetes on perceptual speed and semantic memory was equivalent to the effect of ~6–14 years of age.

Our finding of a relation of diabetes to impaired cognition is consistent with some previously published cross-sectional studies (5,6,9,27–29), but not others (7,8,10,30). Of the four studies that did not find a relation, two had <200 participants (10,30), and a third used only one brief measure of cognition (7). These factors may have limited the power to detect an association between diabetes and cognition.

The basis for the association of diabetes to cognition is uncertain. A vascular process is a plausible basis, given the associations of diabetes with vascular disease (1,31) and of vascular disease with impaired cognition, particularly perceptual speed (32,33). Our study found that diabetes was related to perceptual speed but not to episodic memory, which is typically affected earliest and most prominently in Alzheimer’s disease. This dissociation suggests that diabetes may be affecting cognition through a vascular process rather than through Alzheimer’s disease pathology. Indeed, the associations of diabetes to semantic memory or perceptual speed were no longer statistically significant after controlling for several vascular risk factors. However, controlling for stroke and evidence of vascular disease in other systems (e.g., myocardial infarction) did not alter the association of diabetes to cognition. This, as well as observations from published studies that controlled for some of these factors yet showed associations of diabetes to cognition (6,26,34), raises the possibility that other mechanisms may be involved.

An unexpected finding was that we found a significant interaction of diabetes with current cigarette smoking. The association of diabetes with cognitive impairment was substantially stronger in current smokers compared to those who never smoked or formerly smoked. We interpret these results with caution, as there were only seven individuals with diabetes who smoked. Nevertheless, the model assumptions were found to be adequately met. To our knowledge, no previous research has examined whether smoking or other vascular risk factors modify the relation of diabetes to cognition. The mechanisms underlying this finding remain to be elucidated. Cigarette smoking is known to be associated with several harmful biological processes in addition to its effects on blood vessels, such as atherosclerosis and other changes in vessel wall morphology and function (35). These include oncogene activation and genetic mutations (36), oxidative stress and telomere damage (37), activation of inflammatory processes (38), and metabolic imbalances (39). It is possible that one or more of these processes could interact, either directly or indirectly, with the biological effects of diabetes and result in altered central nervous system function and impaired cognition. In addition, it is possible that other unmeasured factors, vascular or nonvascular, may account for the association of diabetes to cognition.

This study has several strengths. First, data analysis of a relatively large cohort of older individuals enhanced our ability to detect the associations of interest. Second, based on structured clinical evaluations and the use of widely accepted criteria, individuals with dementia were identified and excluded from analyses, allowing the examination of the relation of diabetes to cognition in a cohort of older individuals free of dementia. Third, the use of composite measures of cognitive function, derived from extensive neuropsychological testing, reduced floor and ceiling artifacts and other sources of random variability. Further, these composite measures allowed for the examination of the relation of diabetes to separate cognitive domains. Finally, the clinical evaluations provided detailed medical information that permitted examination of risk factors that might account for or modify the associations of interest.

This study also has several important weaknesses. First, the identification of some variables, including diabetes and smoking, was based partly or wholly on self-report. Further, laboratory data supporting a diagnosis of diabetes were not available. These factors may have lead to incomplete ascertainment of some variables and underestimation of the effect of diabetes on cognitive function. Nevertheless, we found strong associations between diabetes and cognitive function. Second, because the interaction between diabetes and smoking was based on a small number of individuals, it will be important to replicate these findings. Third, data were cross-sectional, negating our ability to examine the relation of diabetes to change in cognition. Longitudinal studies of the relation of diabetes to change in cognitive function, particularly change in different cognitive systems (11), may help elucidate mechanisms underlying these relations.


   Acknowledgments
 
This study was supported by the National Institute on Aging Grants K23 AG23675 (to Z.A.), R01 AG17917, P30 AG10161, and R01 AG022018 (to D.A.B.) and by the Illinois Department of Public Health.

We are indebted to the hundreds of Illinois residents participating in the Rush Memory and Aging Project. We thank the study coordinators Traci Colvin and Tracy Hagman; data and analytic programmers George Dombrowski, Greg Klein, Woojeong Bang, and Todd Beck; and the faculty and staff of the Rush Alzheimer’s Disease Center and Rush Institute for Healthy Aging.


   Footnotes
 
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received for publication October 6, 2005. Accepted for publication December 4, 2005.


   References
TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS
 RESULTS
 CONCLUSIONS
 References
 

  1. Abbott RD, Donahue RP, MacMahon SW, Reed DM, Yano K: Diabetes and the risk of stroke: the Honolulu Heart Program. JAMA 257:949–952, 1987[Abstract]
  2. Arvanitakis Z, Wilson RS, Schneider JA, Bienias JL, Evans DA, Bennett DA: Diabetes mellitus and progression of rigidity and gait disturbance in older persons. Neurology 63:996–1001, 2004[Abstract/Free Full Text]
  3. Ott A, Stolk RP, Hofman A, van Harskamp F, Grobbee DE, Breteler MM: Association of diabetes mellitus and dementia: the Rotterdam Study. Diabetologia 39:1392–1397, 1996[Medline]
  4. Haan MN, Mungas DM, Gonzalez HM, Ortiz TA, Acharya A, Jagust WJ: Prevalence of dementia in older Latinos: the influence of type 2 diabetes mellitus, stroke and genetic factors. J Am Geriatr Soc 51:169–177, 2003[Medline]
  5. Sinclair AJ, Girling AJ, Bayer AJ: Cognitive dysfunction in older subjects with diabetes mellitus: impact on diabetes self-management and use of care services: All Wales Research into Elderly (AWARE) Study. Diabetes Res Clin Pract 50:203–212, 2000[Medline]
  6. Grodstein F, Chen J, Wilson RS, Manson JE, Nurses HS: Type 2 diabetes and cognitive function in community-dwelling elderly women. Diabetes Care 24:1060–1065, 2001[Abstract/Free Full Text]
  7. Bourdel-Marchasson I, Dubroca B, Manciet G, Decamps A, Emeriau JP, Dartigues JF: Prevalence of diabetes and effect on quality of life in older French living in the community: the PAQUID Epidemiological Survey. J Am Geriatr Soc 45:295–301, 1997[Medline]
  8. Lindeman RD, Romero LJ, LaRue A, Yau CL, Schade DS, Koehler KM, Baumgartner RN, Garry PJ: A biethnic community survey of cognition in participants with type 2 diabetes, impaired glucose tolerance, and normal glucose tolerance: the New Mexico Elder Health Survey. Diabetes Care 24:1567–1572, 2001[Abstract/Free Full Text]
  9. U’Ren RC, Riddle MC, Lezak MD, Bennington-Davis M: The mental efficiency of the elderly person with type II diabetes mellitus. J Am Geriatr Soc 38:505–510, 1990[Medline]
  10. Lowe LP, Tranel D, Wallace RB, Welty TK: Type II diabetes and cognitive function: a population-based study of Native Americans. Diabetes Care 17:891–896, 1994[Abstract]
  11. Arvanitakis Z, Wilson RS, Bienias JL, Evans DA, Bennett DA: Diabetes mellitus and risk of Alzheimer disease and decline in cognitive function. Arch Neurol 61:661–666, 2004[Abstract/Free Full Text]
  12. Wilson RS, Barnes LL, Bennett DA: Assessment of lifetime participation in cognitively stimulating activities. J Clin Experiment Neuropsychol 25:634–642, 2003
  13. Bennett DA, Schneider JA, Buchman AS, Mendes de LC, Bienias JL, Wilson RS: The Rush Memory and Aging Project: study design and baseline characteristics of the study cohort. Neuroepidemiol 25:163–175, 2005[Medline]
  14. Medi-Span: Master Drug Data Base Documentation Manual. Indianapolis, IN, Medi-Span, 1995
  15. McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM: Clinical diagnosis of Alzheimer’s disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer’s Disease. Neurology 34:939–944, 1984[Abstract/Free Full Text]
  16. Wilson RS, Barnes LL, Krueger KR, Hoganson G, Bienias JL, Bennett DA: Early and late-life cognitive activity and cognitive systems in old age. J Int Neuropsychol Soc 11:400–407, 2005[Medline]
  17. Morris JC, Heyman A, Mohs RC, Hughes JP, van Belle G, Fillenbaum G, Mellits ED, Clark C: The Consortium to Establish a Registry for Alzheimer’s Disease (CERAD). Part I. Clinical and neuropsychological assessment of Alzheimer’s disease. Neurology 39:1159–1165, 1989[Abstract/Free Full Text]
  18. Wechsler D: Wechsler Memory Scale: Revised Manual. San Antonio, TX, Psychological Corporation, 1987
  19. Albert M, Smith L, Scherr P, Taylor J, Evans D, Funkenstein H: Use of brief cognitive tests to identify individuals in the community with clinically diagnosed Alzheimer’s disease. Int J Neurosci 57:167–178, 1991[Medline]
  20. Wilson RS, Beckett LA, Barnes LL, Schneider JA, Bach J, Evans DA, Bennett DA: Individual differences in rates of change in cognitive abilities of older persons. Psychol Aging 17:179–193, 2002[Medline]
  21. Cooper JA, Sagar HJ: Incidental and intentional recall in Parkinson’s disease: an account based on diminished attentional resources. J Clin Exp Neuropsychol 15:713–731, 1993[Medline]
  22. Smith A: Symbol Digit Modalities Test Manual–Revised. Los Angeles, CA, Western Psychological Services, 1992
  23. Ekstrom RB, French JW, Harman HH, Kermen D: Manual for Kit of Factor: Referenced Cognitive Tests. Princeton, NJ, Educational Testing Service, 1976
  24. Raven JC, Court JH, Raven J: Manual for Raven’s Progressive Matrices and Vocabulary: Standard Progressive Matrices. Oxford, Oxford Psychologists Press, 1992
  25. Rose GA: The diagnosis of ischaemic heart pain and intermittent claudication in field surveys. Bull World Health Org 27:645–658, 1962[Medline]
  26. Crooks VC, Buckwalter JG, Petitti DB: Diabetes mellitus and cognitive performance in older women. Ann Epidemiol 13:613–619, 2003[Medline]
  27. Worrall G, Moulton N, Briffett E: Effect of type II diabetes mellitus on cognitive function. J Fam Pract 36:639–643, 1993[Medline]
  28. Sinclair AJ, Allard I, Bayer A: Observations of diabetes care in long-term institutional settings with measures of cognitive function and dependency. Diabetes Care 20:778–784, 1997[Abstract]
  29. Bruce DG, Casey GP, Grange V, Clarnette RC, Almeida OP, Foster JK, Ives FJ, Davis TM: Cognitive impairment, physical disability and depressive symptoms in older diabetic patients: the Fremantle Cognition in Diabetes Study. Diabetes Res Clin Pract 61:59–67, 2003[Medline]
  30. Cosway R, Strachan MW, Dougall A, Frier BM, Deary IJ: Cognitive function and information processing in type 2 diabetes. Diabet Med 18:803–810, 2001[Medline]
  31. Kannel WB, McGee DL: Diabetes and cardiovascular disease: the Framingham Study. JAMA 241:2035–2038, 1979[Abstract]
  32. Price TR, Manolio TA, Kronmal RA, Kittner SJ, Yue NC, Robbins J, Anton-Culver H, O’Leary DH: Silent brain infarction on magnetic resonance imaging and neurological abnormalities in community-dwelling older adults: the Cardiovascular Health Study: CHS Collaborative Research Group. Stroke 28:1158–1164, 1997[Abstract/Free Full Text]
  33. Schneider JA, Wilson RS, Cochran EJ, Bienias JL, Arnold SE, Evans DA, Bennett DA: Relation of cerebral infarctions to dementia and cognitive function in older persons. Neurology 60:1082–1088, 2003[Abstract/Free Full Text]
  34. Kalmijn S, Feskens EJ, Launer LJ, Stijnen T, Kromhout D: Glucose intolerance, hyperinsulinaemia and cognitive function in a general population of elderly men. Diabetologia 38:1096–1102, 1995[Medline]
  35. Esen AM, Barutcu I, Acar M, Degirmenci B, Kaya D, Turkmen M, Melek M, Onrat E, Esen OB, Kirma C: Effect of smoking on endothelial function and wall thickness of brachial artery. Circ J 68:1123–1126, 2004[Medline]
  36. Tsurutani J, Castillo SS, Brognard J, Granville CA, Zhang C, Gills JJ, Sayyah J, Dennis PA: Tobacco components stimulate Akt-dependent proliferation and NFkappaB-dependent survival in lung cancer cells. Carcinogenesis 26:1182–1195, 2005[Abstract/Free Full Text]
  37. Valdes AM, Andrew T, Gardner JP, Kimura M, Oelsner E, Cherkas LF, Aviv A, Spector TD: Obesity, cigarette smoking, and telomere length in women. Lancet 366:662–664, 2005[Medline]
  38. Gan WQ, Man SF, Sin DD: The interactions between cigarette smoking and reduced lung function on systemic inflammation. Chest 127:558–564, 2005[Abstract/Free Full Text]
  39. Holm IA, Manson JE, Michels KB, Alexander EK, Willett WC, Utiger RD: Smoking and other lifestyle factors and the risk of Graves’ hyperthyroidism. Arch Intern Med 165:1606–1611, 2005[Abstract/Free Full Text]

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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Diabetes Diabetes Care Clinical Diabetes Diabetes Spectrum