Brss
17
Barbara Fletcher, RN, MN, FAAN Clinical Associate Professor University of North Florida, Department
of Nursing Jacksonville Beach, Florida
Meg Gulanick, PhD, RN Associate Professor Niehoff School of Nursing Loyola University Chicago Chicago, Illinois
Cindy Lamendola, RN, MSN, ANP Adult Nurse Practitioner, Division of
Endrocrinology Stanford University School of Medicine Stanford, California
Genetic, environmental, and metabolic risk factors are interrelated and contribute to the development of type 2 diabetes mellitus. A strong family history of diabetes mellitus, age, obesity, and physical inactivity identify those individuals at highest risk. Minority populations are also at higher risk, not only because of family history and genetics, but also because of adaptation to American environmental influences of poor dietary and exercise habits. Women with a history of gestational diabetes as well as their children are at greater risk for progressing to type 2 diabetes mellitus. Insulin resistance increases a person’s risk for developing impaired glucose tolerance and type 2 diabetes. Individuals who have insulin resistance share many of the same risk factors as those with type 2 diabetes. These include hyperinsulinemia, atherogenic dyslipidemia, glucose intolerance, hypertension, prothrombic state, hyperuricemia, and polycystic ovary syndrome. Cur- rent interventions for the prevention and retardation of type 2 diabetes mellitus are those targeted towards modifying environmental risk factors such as reducing obesity and promoting physical activity. Awareness of risk factors for developing type 2 diabetes will promote screening, early de- tection, and treatment in high-risk populations with the goal of decreasing both microvascular and macrovascular complications. Key words: environmental factors, lifestyle, risk factors, type 2 diabetes
tries are at much higher risk. Ethnicity, ge- netics, and lifestyle play an important role in determining a person’s risk factors for type 2 diabetes. The importance of risk fac- tor identification is to promote diabetes screening to initiate prevention measures. Early detection and treatment of type 2 diabetes enhances prevention of micro- vascular and macrovascular complications associated with this disease.
Several terms require definition as a basis for this article. Risk factors are those aspects of an individual’s lifestyle, envi- ronment, or genetic traits that are known through epidemiologic study to be associ- ated with occurrence of disease. Preva- lence of disease is the number of people known to have the disease (in this case, type 2 diabetes), whether diagnosed or un- diagnosed, at a particular time. Incidence refers to the number of people diagnosed with the disease for the first time within a specific time frame.1
Identification of risk factors for type 2 diabetes has been challenging because the genetic and lifestyle factors are interre- lated and associated with insulin resis- tance and metabolic conditions.2–3 These
Risk Factors for Type 2 Diabetes Mellitus
J Cardiovasc Nurs 2002;16(2):17–23 © 2002 Aspen Publishers, Inc.
W hile there has been a lack of consen-sus over the years on how best to define, diagnose, and classify type 2 dia- betes mellitus, research in identifying risk factors for diabetes has progressed more clearly. It has been known for years that not all populations or persons present with the same risk for diabetes. For exam- ple, populations in developing countries as well as disadvantaged and minority populations in more industrialized coun-
Article 2 11/21/01 7:19 PM Page 17
interrelationships are depicted in Fig 1. Groups at highest risk are those persons with a strong family history, persons of older age, those who are obese, and those who are physically inactive. Type 2 dia- betes is known to be more predominant in the Native American, Hispanic American, African American, Pacific Islander, and Asian American populations versus those from European descent.2 Since type 2 dia- betes is characterized by insulin resis- tance, people with this disease have the as- sociated metabolic abnormalities, such as hypertension, elevated triglycerides, and low HDL cholesterol, that are also identi- fied as risks factors for type 2 diabetes.3
Women with a history of gestational dia- betes mellitus, or who delivered a baby weighing more than 9 lbs., have greater risk for developing type 2 diabetes as well as persons with impaired glucose toler-
ance (IGT) or impaired fasting glucose (IFG).1,2,4 The greater the number of risk factors an individual has, the greater the chance of developing type 2 diabetes and its associated complications. This article will highlight the more traditional risk fac- tors for diabetes.
FAMILY HISTORY
It is well accepted that type 2 diabetes is an inherited condition. Though a specific gene has yet to be found, the nearly 100% concordance rates of diabetes seen in iden- tical twins, the aggregation in families, and the high rates seen in ethnic and racial populations lend strong support for this hypothesis. The Framingham Offspring Study found that the risk for type 2 dia- betes among offspring with a single parent with diabetes was 3.5 fold greater, and for
18 THE JOURNAL OF CARDIOVASCULAR NURSING/JANUARY 2002
Fig 1. Risk factors for developing type 2 diabetes mellitus and the metabolic abnormalities associ- ated with insulin resistance. Note: * GDM (gestational diabetes mellitus) may be influenced by ge- netics, lifestyle, insulin resistance, or a combination thereof. Source: Data from American Diabetes Association, Clinical Practice Recommendations 2001, vol. 24: S21–S24.
Article 2 11/21/01 7:19 PM Page 18
those with two diabetic parents was 6-fold greater when compared with offspring without parental diabetes.5 No differences were noted in maternal versus paternal risk of transmission, though interestingly the offspring with maternal diabetes were more likely to have milder forms of glu- cose intolerance as compared to paternal transmission.
AGE
Type 2 diabetes has been known for years as “adult onset,” or “maturity-onset,” emphasizing that the prevalence of type 2 diabetes increases with age. Of persons 65 years or older, 18.4% of all people in this age group have diabetes.1 Many surveys re- port a leveling off or slight decline at age 75 or greater.6 It is noteworthy that in the past, the age of 45 years has been used as an im- portant cut-off point in estimating the prevalence of diabetes. However, in the last eight years, younger adults between the ages of 30–39 have had a startling 70% rise in type 2 diabetes.1 Rates for the next age group, 40– 49 years, rose a dramatic 40%. These startling statistics are blamed on cur- rent lifestyle patterns that result in excess body weight and less physical activity.
RACIAL/ ETHNIC
Minorities in the United States exhibit higher prevalence for diabetes (2–6 times greater than that of white persons)7. The Third National Health and Nutrition Sur- vey—1988–1994 (NHANES III) showed the prevalence rate of diabetes to be 1.7 times higher for non-Hispanic blacks than for whites of similar age.1,6 Controlling for obe- sity did not affect this increased risk.7 One in four black women aged 55 years or older has diabetes. This is twice the rate for age matched white women. Black females have the highest diabetes related deaths com- pared with other minorities.1
All Hispanic populations, who com- prise the fastest growing minority popula- tion in the United States, have greater prevalence rates of type 2 diabetes than non-Hispanic whites.6 Statistics vary de- pending on the communities studied. Over- all, diabetes prevalence rates for Mexican- Americans are estimated at 2 to 5 times that of the non-Hispanic white population, with the greatest prevalence rates found for Puerto Ricans and Hispanics living in the southwest, where half of the adults are affected in some cities.6–8 Limited data are available for prevalence rates for Asian Americans and Pacific Islanders.
According to the Centers for Disease Control and Prevention (CDC), Native Amer- icans have a disproportionately higher prevalence of diabetes—2.8 times that of whites of similar age.7,9 Indeed, the highest prevalence of diabetes in the world has been found among the Pima Indians in Arizona, where approximately 1 of every 2 adults has type 2 diabetes. The CDC study of all Native Americans across the United States conducted between 1990–1997 re- ported that the prevalence of diabetes in- creased almost 30% during that time pe- riod. These increases were evident across all age groups.9 But even within the high risk populations differences in rates of type 2 diabetes may vary depending on modifiable risk factors such as exercise and weight. For example, the prevalence of type 2 diabetes is six times higher in the Pima Indians living in Arizona than the Pima Indians living in Rural Mexico. One explanation may be that the mean body mass index is 8 kg/m2 greater among the Pima Indians living in Arizona.3
These minority populations are at higher risk, not simply because of their family history and genetic heritage, but because of the increased number of environmental risk factors they exhibit from having “westernized” and taken on the American habits of high calorie diets and sedentary lifestyle.7,9 Other contributing factors, such
Risk Factors 19
Article 2 11/21/01 7:19 PM Page 19
as lower economic status and access barri- ers to health care, may negatively impact these groups.7–8 This remains an under- studied topic. NHANES III data were ex- amined for racial and ethnic differences in health outcomes for persons with type 2 diabetes.10 Though small differences by race and ethnicity were found in health care access and utilization, along with health outcomes, the most striking finding was the overwhelming suboptimal health status for all diabetics, regardless of race or ethnicity. Socioeconomic status was not a major variable; rather a multiplicity of fac- tors impacted these outcomes.
GESTATIONAL DIABETES MELLITUS (GDM)
Women who have a history of GDM are at greater risk for future diabetes as are their children. Gestational diabetes is defined as any degree of glucose intolerance with its onset or first recognition occurring during pregnancy.11 This definition does not ex- clude the possibility that undiagnosed glu- cose intolerance may have preceded the pregnancy. The incidence of GDM averages around 4% of all US pregnancies, though the range is much wider (1–14%) depend- ing on the racial or ethnic groups studied, as well as the prevalence of obesity.12–13 The progression from GDM to diabetes may be partly explained by more universal screen- ing and detection along with the trend for older women to have children.14 The Nurses Health Study examined pregravid determinants of GDM. A family history of diabetes, advanced maternal age, nonwhite ethnicity, higher BMI, weight gain in early adulthood, and cigarette smoking were found to predict a woman’s risk for GDM.13
Rates of progression of GDM to diabetes varies, with a 5% risk of type 2 diabetes during the 3–6 month postpartum period, increasing up to 47% at 5-year follow- up.15 Review of additional studies reported a 40% occurrence of diabetes at 15 years in women with prior GDM.1,15 The devel- opment of postpartum diabetes is influ-
enced by the degree of obesity prior to preg- nancy, the need for insulin treatment dur- ing pregnancy, and higher glucose readings during oral glucose tolerance testing.15 Eth- nicity also strongly affects progression to diabetes after a GDM pregnancy, with high- risk ethnic groups often reporting 50% of women becoming diabetic within 5 years.14
Of course, the confounding variables of obesity and physical inactivity reported in these ethnic groups, as well as in all women, affect progression to diabetes.
IMPAIRED FASTING GLUCOSE (IFG) AND IMPAIRED GLUCOSE TOLERANCE (IGT)
The American Diabetes Association de- fines IFG and IGT as an intermediate cate- gory between normoglycemia and diabetes. Criteria for IFG include individuals with a fasting blood glucose level of 110 mg/dl to 125 mg/dl. IGT is determined from a 2 hour oral glucose tolerance test reading of $140 mg/dl but ,200 mg/dl.11 Individuals with IGT demonstrate normal glycemic levels throughout most of their daily lives, with the metabolic impairment only noted during glucose tolerance testing. IGT indi- cates a higher than normal risk of progres- sion to type 2 diabetes, ranging from 2.3 to 11% per year, especially among nonwhite racial and ethnic groups. Prevalence is greater among women in each minority group.6,7,11 Insulin resistance and sub- sequent IGT are directly involved in the pathogenesis of diabetes. Data from six prospective studies among diverse popula- tions revealed that the strongest predictors of progression from IGT to type 2 diabetes were elevated fasting and 2-hour post chal- lenge glucose levels.16 The detection of IGT is particularly significant since it signals long standing insulin resistance and is a strong risk factor for type 2 diabetes.
INSULIN RESISTANCE
Insulin resistance is a defect in the abil- ity of insulin to take up glucose into the
20 THE JOURNAL OF CARDIOVASCULAR NURSING/JANUARY 2002
Article 2 11/21/01 7:19 PM Page 20
muscle cell. Despite being genetically de- termined, it is greatly aggravated by obesity and physical inactivity.17 During the initial phases of insulin resistance, the pancre- atic beta cells are able to maintain normal glycemic control through an increased pro- duction of insulin, thereby making these in- dividuals hyperinsulinemic.18–19 However, when individuals can no longer maintain normal glycemia from this compensatory mechanism, they progress to development of type 2 diabetes.18
Research suggests that insulin resistance is a multi-system disorder that is corre- lated with multiple metabolic abnormali- ties. It is not surprising that those individu- als who are insulin resistant share the same risk factors as those who are at risk for type 2 diabetes. Indeed, insulin resis- tance predisposes individuals to both dia- betes and CVD.18–20 Factors that contribute to insulin resistance are genetics,21 obe- sity,22 physical inactivity,23 and age.24 Ab- dominal obesity often accompanies in- sulin resistance.25 Although there is a strong correlation with insulin resistance and obesity, not all obese people are in- sulin resistant.26–27 Metabolic risk factors that commonly occur in persons with insulin resistance are hyperinsulinemia, atherogenic dyslipidemia (elevated tri- glycerides and low HDL-C), glucose intol- erance, hypertension, prothrombotic state, hyperuricemia, and polycystic ovary syn- drome.19,20,28 The clinical picture of insulin resistance is depicted in Fig l. Refer also to Quinn’s excellent description of the three stages of insulin resistance in the pathogen- esis of type 2 diabetes in the lead article of this issue.
OBESITY AND PHYSICAL INACTIVITY
An estimated 97 million US adults are overweight (body mass index (BMI 5 25– 29.9 kg/m2) or obese (BMI 30 kg/m2 or . ).29
Despite current recommendations to exer- cise at a moderate level for 30–45 minutes on most days of the week, 75% of US adults engage in minimal physical activity
(such as walking only 15 to 20 minutes a day on a regular basis) or less.30 These life habits, along with the aging of the popula- tion, contribute to the growing prevalence of diabetes.31 Obesity alone, especially ab- dominal adiposity, is a major determinant of the development of type 2 diabetes, causing it to occur at an earlier age.32 When obesity is compounded by physical inac- tivity, the risk for type 2 diabetes dramati- cally increases.33 People who are obese and have insulin resistance can increase insulin sensitivity by weight loss; however those people who are obese without in- sulin resistance do not improve their in- sulin sensitivity with similar weight loss.34
Mechanisms for the improvement in in- sulin sensitivity with weight loss are com- plex and not completely understood at this time.35–36
Limited data in men with type 2 diabetes show that a low level of physical activity is an independent predictor of all cause mor- tality.37– 39 Exercise increases insulin sensi- tivity and glucose tolerance, as well as im- proves blood lipid profiles in persons with type 2 diabetes.40– 42 Exercise as an adjunct to diet yields greater and more sustained weight loss in obese subjects with type 2 diabetes43 and exercise improves insulin sensitivity and reduces body weight.44 The combination of weight loss and exercise enhances insulin sensitivity and improves glucose control, thus facilitating the risk reduction in type 2 diabetes.
In summary, the profile of individuals most at risk for developing type 2 diabetes is clear. Although genetic predisposition exhibits the strongest influence, attention to the modifiable risk factors is strongly warranted. It is clear that physical activity and weight management have a positive influence on retarding or halting the pro- gression to type 2 diabetes. As nurses, our role is to be to be aware of what popula- tions will be at higher risk for developing type 2 diabetes and to be proactive in pro- moting influential lifestyle habits with the goal of reducing the incidence of IGT and type 2 diabetes and its complications.
Risk Factors 21
Article 2 11/21/01 7:19 PM Page 21
REFERENCES
22 THE JOURNAL OF CARDIOVASCULAR NURSING/JANUARY 2002
1. Centers for Disease Control and Preven- tion. (2000) www.cdc.gov/diabetes/statis- tics. Feb 2001.
2. American Diabetes Association. Clinical Practice Recommendations 2001.vol 24: S21–S24.
3. Reaven G, Laws A (Ed). Insulin resistance: The metabolic syndrome X. Humana Press, Totowa, NJ; 1999.
4. American Diabetes Association. Screen- ing for type 2 diabetes. Diabetes Care. 2000;23:S20–S23.
5. Meigs JB, Cupples LA, Wilson, PW. Parental transmission of type 2 diabetes: the Framingham Offspring Study. Dia- betes. 2000;49:2201–2207.
6. Harris MI, Flegal KM, Cowie CC, et al. Prevalence of diabetes, impaired fasting glucose, and impaired glucose tolerance in U.S. adults. The Third National Health and Nutrition Examination Survey, 1988– 1994. Diabetes Care. 1998;21:518–524.
7. Carter JS, Pugh JA, Monterrosa, A. Non- insulin-dependent diabetes mellitus in minorities in the United States. Ann Intern Med. 1996;125:221–232.
8. Hispanic health in the United States. Council on Scientific Affairs. JAMA. 1991;265:248–252.
9. Burrows NR, Geiss LS, Engelgau MM, Acton KJ. Prevalence of diabetes among Native Americans and Alaska Natives, 1990–1997: an increasing burden. Dia- betes Care. 2000;23:1786–1790.
10. Harris M. Racial and ethnic differences in health care access and health outcomes for adults with type 2 diabetes. Diabetes Care. 2001;24(3):454– 459.
11. Report of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. Diabetes Care. 1997;20:1183– 1197.
12. Engelgau MM, Herman WH, Smith PJ, German RR, Aubert RE. The epidemiol- ogy of diabetes and pregnancy in the U.S., 1988. Diabetes Care. 1995;18:1029–1033.
13. Solomon CG, Willett WC, Carey VJ, et al. A prospective study of pregravid determi- nants of gestational diabetes mellitus. JAMA. 1997;278:1078–1083.
14. Dornhorst A, Rossi M. Risk and preven- tion of type 2 diabetes in women with ges- tational diabetes. Diabetes Care. 1998;21 Suppl 2:B43–B49.
15. Bloomgarden, ZT. American Diabetes As- sociation 60th Scientific Sessions, 2000: diabetes and pregnancy. Diabetes Care. 2000;23:1699–1702.
16. Edelstein SL, Knowler WC, Bain RP, et al. Predictors of progression from impaired glucose tolerance to NIDDM: an analysis of six prospective studies. Diabetes. 1997; 46:701–710.
17. Reaven GM. Insulin resistance: a chicken that has come to roost. Ann N Y Acad Sci. 1999;892:45–57.
18. Reaven G. Banting lecture 1988 the role of insulin resistance in human disease. Dia- betes. 1988;37:1595–1607.
19. Reaven G. Pathophysiology of insulin re- sistance in human disease. Physiological Review. 1995;473–486.
20. Reaven GM, Lithell H, Landsberg L. Hypertension and associated metabolic abnormalities—the role of insulin resist- ance and the sympathoadrenal system. N Engl J Med. 1996;334:374–381.
21. Warram JH, Martin BC, Krolewski AS, Soeldner JS, Kahn CR. Slow glucose re- moval rate and hyperinsulinemia precede the development of type II diabetes in the offspring of diabetic parents. Ann Intern Med. 1990;113:909–915.
22. Bogardus C, Lillioja S, Mott D, Reaven GR, Kashiwagi A, Foley JE. Relationship be- tween obesity and maximal insulin-stim- ulated glucose uptake in vivo and in vitro in Pima Indians. J Clin Invest. 1984; 73: 800 – 805.
23. Perseghin G, Price TB, Petersen KF, et al. Increased glucose transport-phosphoryla- tion and muscle glycogen synthesis after exercise training in insulin-resistant sub- jects. N Engl J Med. 1996;335:1357–1362.
24. Rowe JW, Minaker KL, Pallotta JA, Flier JS. Characterization of the insulin resistance of aging. J Clin Invest. 1983;71:1581–1587.
25. Abate N, Garg A, Peshock RM, Stray-Gun- dersen J, Grundy SM. Relationships of generalized and regional adiposity to
Article 2 11/21/01 7:19 PM Page 22
Risk Factors 23
insulin sensitivity in men. J Clin Invest. 1995;96:88–98.
26. Ferrannini E, Natali A, Bell P, et al. On be- half of the European Group for the Study of Insulin Resistance (EGIR). Insulin re- sistance and hypersecretion in obesity. J Clin Invest. 1997;100:1166–1173.
27. Jones C, Abbasi F, Carantoni M, Polonsky K, Reaven G. Roles of insulin resistance and obesity in regulation of plasma in- sulin concentrations. Am J Physiol En- docrinol Metab. 2000;278:E501–E508.
28. Yeni-Komshian H, Carantoni M, Abbasi F, Reaven G. Relationship between several surrogate estimates of insulin resistance and Quantification of insulin-mediated glucose disposal in 490 healthy nondia- betic volunteers. Diabetes Care. 2000;23; 171–175.
29. National Heart Lung and Blood Institute. Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults. National Heart Lung and Blood Institute. 1998.
30. Physical activity and cardiovascular health. NIH Consensus Development Panel on Physical Activity and Cardiovascular Health. JAMA. 1996;276:241–246.
31. Grundy SM, Benjamin IJ, Burke GL, et al. Diabetes and cardiovascular disease: a statement for healthcare professionals from the American Heart Association. Circula- tion. 1999;100:1134–1146.
32. Haffner SM. Obesity and the metabolic syndrome: the San Antonio Heart Study. Br J Nutr. 2000;83 Suppl 1:S67–S70.
33. Diabetes mellitus: a major risk factor for car- diovascular disease. A joint editorial state- ment by the American Diabetes Associa- tion; The National Heart, Lung, and Blood Institute; The Juvenile Diabetes Foundation International; The National Institute of Dia- betes and Digestive and Kidney Diseases; and The American Heart Association. Cir- culation. 1999;100:1132– 1133.
34. Mc Laughlin T, Abbasi F, Kim HS, Lamen- dola C, Schaaf P, Reaven G. Relationship between insulin resistance, weight loss, and coronary heart disease in healthy, obese women. Metabolism. 2001 July;50 (7):795–800.
35. McLaughlin T, Abbasi F, Lamendola C, Kim HS, Reaven G. Metabolic changes fol-
lowing sibutramine-assisted weight loss in obese individuals: role of plasma free fatty acids in the insulin resistance of obesity. Metabolism. 2001 July;50(7):819 – 824.
36. Kelley D, Goodpaster B, Wing R, Si- moneau J-A. Skeletal muscle fatty acid metabolism in association with insulin re- sistance, obesity, and weight loss. Am J Physiol. 1999;277(6 Pt 1):E1130–E1141.
37. Ford ES, DeStefano F. Risk factors for mortality from all causes and from coro- nary heart disease among persons with di- abetes. Findings from the National Health and Nutrition Examination Survey I Epi- demiologic Follow-up Study. Am J Epi- demiol. 1991;133:1220–1230.
38. Wei M, Gibbons LW, Kampert JB, Nichaman MZ, Blair SN. Low cardiorespi- ratory fitness and physical inactivity as predictors of mortality in men with type 2 diabetes. Ann Intern Med. 2000;132: 605–611.
39. Wannamethee SG, Shaper AG, Alberti KG. Physical activity, metabolic factors, and the incidence of coronary heart disease and type 2 diabetes. Arch Intern Med. 2000;160:2108–2116.
40. Manson JE, Hu FB, Rich-Edwards, JW et al. A prospective study of walking as com- pared with vigorous exercise in the pre- vention of coronary heart disease in women. N Engl J Med. 1999;341:650–658.
41. Goodyear L, Kahn B. Exercise, glucose transport and insulin sensitivity. Ann Rev Med. 1998;49:235–261.
42. Mayer-Davis E, D’Agostino R, Karter A, Haffner S, Reweres M, Saad M, Bergman R. for the IRAS investigators. Intensity and amount of physical activity in rela- tion to insulin sensitivity. JAMA. 1998; 279:669– 674.
43. Wing RR, Epstein LH, Paternostro-Bayles M, Kriska A, Nowalk MP, Gooding W. Ex- ercise in a behavioral weight control pro- gramme for obese patients with Type 2 (non-insulin-dependent) diabetes. Dia- betologia. 1988;31:902–909.
44. Yamanouchi K, Shinozaki T, Chikada K, et al. Daily walking combined with diet therapy is a useful means for obese NIDDM patients not only to reduce body weight but also to improve insulin sensitivity. Diabetes Care. 1995;18:775–778.
Article 2 11/21/01 7:19 PM Page 23
Copyright of Journal of Cardiovascular Nursing is the property of Lippincott Williams & Wilkins -- Nursing
and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright
holder's express written permission. However, users may print, download, or email articles for individual use.