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RESEARCH AND PRACTICE |
The authors are with the Division of Clinical Epidemiology, Geneva University Hospital, Geneva, Switzerland.
Correspondence: Requests for reprints should be sent to Alfredo Morabia, MD, PhD, Division of Clinical Epidemiology, Geneva University Hospital, 25, Rue Micheli-du-Crest, CH-1211 Geneva 14 Switzerland (e-mail: a.morabia{at}hcuge.ch).
| ABSTRACT |
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Increases in obesity, hypercholesterolemia, and diabetes may be under way in Europe. We have reported the only data available from the 1990s for continuous monitoring of chronic disease risk factors in random samples of a general European population. In random surveys (19932003) of 6164 men and 6107 women in Geneva, overweight and obesity combined increased in both men and women; hypercholesterolemia prevalence also rose; diabetes treatment increased in men. Only population-based interventions can prevent the impending epidemic of obesity-related disorders.
| INTRODUCTION |
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A wider epidemic of metabolic disorders may be under way in Geneva, characterized by concurrent, parallel trends in obesity, hypercholesterolemia, and diabetes. Geneva has a relatively low prevalence of obesity,9 so the situation may be worse in other European populations.
| METHODS |
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On the day of the mobile clinic appointment, each participant undergoes a physical examination. Weight and standing height are measured in subjects who are dressed but not wearing shoes (medical scale, precision=0.5 kg; medical gauge, precision=1 cm). Until 1998, total cholesterol was measured in plasma from capillary blood taken from the fingertip of nonfasting subjects with dry chemistry analyzers (Reflotron, Roche Diagnostic, Basel, Switzerland). Thereafter, it was assayed in fasting venous blood (Bayer Technicon Diagnostics, Brussels, Belgium) because substantial progressive underestimation in Reflotron capillary total cholesterol compared with the nondry chemistry laboratory measurement was observed (biases +0.08, 0.17, 0.27, and 0.60 mmol/L in 1999200210). Overall, 57% of the Reflotron capillary total cholesterol measurements for 894 hypercholesterolemic (see next paragraph) patients underestimated laboratory venous total cholesterol (2%, 57%, 71%, and 98% in 1999200210). Monthly quality controls for both methods were performed by the Swiss Center for Quality Control in Clinical Chemistry and Hematology.
The risk factors were defined as follows: (1) relative weight in terms of body mass index (BMI, kg/m2)overweight=25
BMI<30, obese=BMI
30; and (2) hypercholesterolemia: total plasma cholesterol
6.5 mmol/L (approximately 250 mg/dL) or self-report of taking medication for high cholesterol. Participants also were asked if they were receiving a drug therapy for diabetes.
Risk factor prevalence trends (individual-level data, mean age adjusted) were assessed with both quarterly (44 time points) and annual (11 time points) linear regression models. The results were very similar, so annual trends are reported here. The linear regression slope represented the annual change in prevalence, and the associated (2-tailed) P value tested the null hypothesis that the slope was 0 (no trend). In addition, annual, mean age-adjusted prevalences (aggregated data) provided some idea of background sampling fluctuations.11
Six gender-specific prevalence rates of being at risk due to having (1) both high relative weight (i.e., being either overweight (only), obese, or overweight/obese) and hypercholesterolemia or (2) high relative weight or hypercholesterolemia were compared between the diabetes treatment (no or yes) subgroups with Fisher exact tests.
| RESULTS |
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Among men, diabetes treatment prevalence increased significantly (from 2% to 5%; trend P < .001). Among women, there was no evidence of a sustained increase in diabetes treatment prevalence (all prevalence rates = 1%; trend P = .56).
The small fraction of either gender receiving treatment for diabetes was significantly more likely to have at least 1 of the other 2 risk factors (high relative weight, high cholesterol) compared with their nontreated counterparts (men: P<.05 for all 6 comparisons; women: P<.01 for 5 of 6 comparisons; not shown otherwise).
| DISCUSSION |
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These trends might have been overlooked without the unique, ongoing system of continuous surveillance of health determinants in Geneva. Reports on trends normally rely on periodic local or national surveys, usually repeated within intervals of years.13 Because of random sampling variation in survey responses, reliance on data from a limited number of time points in a decade can be misleading. However, trends based on many more closely spaced time points can be identified clearly and interpreted with more confidence than if they were based on fewer time points spaced at much longer intervals.
The "obesity epidemic" might be a harbinger of a wider epidemic of metabolic disorders. The health effects of overweight and obesity on hypercholesterolemia, hypertension, and diabetes are well established.3 They incur increases in a wide range of chronic disorders and declines in life expectancy.
Feasible ways to combat the impending epidemic exist. It has been proposed that an excess intake of 420 kJ/day (100 kcal/day) is responsible for the increasing relative weight observed in many populations. The latter amount of energy can be expended, on average, only if the public health objective is to make populations become globally more active.14
| Acknowledgments |
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Human Participant Protection
The study was approved by the Geneva University ethics committee.
| Footnotes |
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Contributors
A. Morabia initiated and developed the study and has directed the Bus Santé survey since its inception in 1992. M. C. Costanza designed, performed, and interpreted the statistical analyses. Both authors contributed equally to the origination and writing of the brief.
Accepted for publication June 11, 2004.
| References |
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2. Hill JO, Wyatt HR, Reed GW, Peters JC. Obesity and the environment: where do we go from here? Science. 2003;299:853855.
3. Manson JE, Skerrett PJ, Greenland P, VanItallie TB. The escalating pandemics of obesity and sedentary lifestyle: a call to action for clinicians. Arch Intern Med. 2004;164:249258.
4. Mokdad AH, Ford ES, Bowman BA, et al. Diabetes trends in the U.S.: 19901998. Diabetes Care. 2000;23:12781283.
5. Mokdad AH, Serdula MK, Dietz WH, Bowman BA, Marks JS, Koplan JP. The spread of the obesity epidemic in the United States, 19911998. JAMA. 1999; 282:15191522.
6. Flegal KM, Carroll MD, Ogden CL, Johnson CL. Prevalence and trends in obesity among US adults, 19992000. JAMA. 2002;288:17231727.
7. Galobardes B, Costanza MC, Bernstein MS, Delhumeau CH, Morabia A. Trends in risk factors for the major "lifestyle-related diseases" in Geneva, Switzerland, 19932000. Ann Epidemiol. 2003;13:537540.[CrossRef][ISI][Medline]
8. Galobardes B, Costanza MC, Bernstein MS, Delhumeau C, Morabia A. Trends in risk factors for lifestyle-related diseases by socioeconomic position in Geneva, Switzerland, 19932000: health inequalities persist. Am J Public Health. 2003;93:13021309.
9. Beer-Borst S, Morabia A, Hercberg S, et al. Obesity and other health determinants across Europe: the EURALIM project. J Epidemiol Community Health 2000;54:424430.
10. Costanza MC, Wolff H, James RW, Morabia A. Improving imprecise cholesterol monitoring and screening tests. J Clin Epidemiol. In press.
11. Costanza MC. Estimating and approximating prevalence trends. Soz Praventivmed. 2004;49:224226.[ISI][Medline]
12. Beer-Borst S, Hercberg S, Morabia A, et al. Dietary patterns in six European populations: results from EURALIM, a collaborative European data harmonization and information campaign. Eur J Clin Nutr. 2000; 54:253262.[CrossRef][ISI][Medline]
13. Morabia A. Worldwide surveillance of risk factors to promote global health. Am J Public Health. 2000;90: 2224.
14. Morabia A, Costanza MC. Does walking 15 minutes per day keep the obesity epidemic away? Simulation of the efficacy of a populationwide campaign. Am J Public Health. 2004;94:437440.
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