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Published online January 9, 2008
Diabetes Care 31:805-807, 2008
DOI: 10.2337/dc07-1117
© 2008 by the American Diabetes Association
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Cardiovascular and Metabolic Risk
Original Research

Effect of Lifestyle Intervention on the Occurrence of Metabolic Syndrome and its Components in the Finnish Diabetes Prevention Study

Pirjo Ilanne-Parikka, MD1,2, Johan G. Eriksson, MD, PHD3,4, Jaana Lindström, PHD3, Markku Peltonen, PHD3, Sirkka Aunola, PHD5, Helena Hämäläinen, MD, PHD6, Sirkka Keinänen-Kiukaanniemi, MD, PHD7,8,9, Mauri Laakso, MD7,8,10, Timo T. Valle, MD3, Jorma Lahtela, MD, PHD11, Matti Uusitupa, MD, PHD12, Jaakko Tuomilehto, MD, PHD3,4 on behalf of the Finnish Diabetes Prevention Study Group

1 Diabetes Center, Finnish Diabetes Association, Tampere, Finland
2 Department of Research Administration, Pirkanmaa Hospital District, Tampere, Finland
3 Diabetes Unit, Department of Health Promotion and Chronic Disease Prevention, National Public Health Institute, Helsinki, Finland
4 Department of Public Health, University of Helsinki, Helsinki, Finland
5 Department of Health and Functional Capacity, Laboratory for Population Research, National Public Health Institute, Turku, Finland
6 Research Department, Social Insurance Institution, Turku, Finland
7 Department of Public Health Science and General Practice, University of Oulu, Oulu, Finland
8 Department of Sport Medicine, Oulu Deaconess Institute, Oulu, Finland
9 Oulu Health Centre, Oulu, Finland
10 Unit of General Practice, Oulu University Hospital, Oulu, Finland
11 Department of Internal Medicine, Tampere University Hospital, Tampere, Finland
12 Department of Public Health and Clinical Nutrition, University of Kuopio, Kuopio, Finland

Address correspondence and reprint requests to Pirjo Ilanne-Parikka, Matinkatu 6, FIN 33900 Tampere, Finland. E-mail: pirjo.ilanneparikka{at}diabetes.fi


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
OBJECTIVE—The aim of this secondary analysis of the Finnish Diabetes Prevention Study was to assess the effects of lifestyle intervention on metabolic syndrome and its components.

RESEARCH DESIGN AND METHODS—A total of 522 middle-aged overweight men and women with impaired glucose tolerance were randomized into an individualized lifestyle intervention group or a standard care control group. National Cholesterol Education Program criteria were used for the definition of metabolic syndrome.

RESULTS—At the end of the study, with a mean follow-up of 3.9 years, we found a significant reduction in the prevalence of metabolic syndrome in the intervention group compared with the control group (odds ratio [OR] 0.62 [95% CI 0.40–0.95]) and in the prevalence of abdominal obesity (0.48 [0.28–0.81]).

CONCLUSIONS—The results suggest that lifestyle intervention may also reduce risk of cardiovascular disease in the long run.

Abbreviations: DPS, Finnish Diabetes Prevention Study • IGT, impaired glucose tolerance


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
Recent studies (14) have shown that lifestyle intervention reduces the risk of progression from impaired glucose tolerance (IGT) to manifest type 2 diabetes. The aim of this secondary analysis of the Finnish Diabetes Prevention Study (DPS) was to assess the effects of lifestyle intervention on metabolic syndrome and its components.


    RESEARCH DESIGN AND METHODS—
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
The DPS design, subjects, and methods applied have previously been described (2,5,6). Altogether, 522 middle-aged (mean age 55 ± 7 years) and overweight (mean BMI 31.2 ± 4.6 kg/m2) men (n = 172) and women (n = 350) with IGT were randomized into either an intensive lifestyle intervention group or a standard care control group. Blood samples were collected and an oral glucose tolerance test was performed at baseline and at each annual visit. Updated National Cholesterol Education Program 2005 criteria (7) were used for the definition of metabolic syndrome. Data were analyzed using SPSS (version 11.5; SPSS, Chicago, IL). For those participants who developed diabetes according to the World Health Organization guidelines of 1985 (8) or who dropped out during the study, the measurements from the last observation were used as the final end value. Wilcoxon's nonparametric test was used to compare the prevalence of metabolic syndrome and its components within the groups. Regression analyses adjusted for sex, age, blood pressure and cholesterol medications, and baseline status were applied to compare the prevalence of metabolic syndrome and its components between the groups.


    RESULTS—
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
The prevalence of metabolic syndrome decreased during the first year from 74.0 to 58.0% vs. from 74.0 to 67.7% (P = 0.018 for the change between the groups) in the intervention and control groups, respectively. At the end of the study, 62.6% of subjects in the intervention group and 71.2% of subjects in the control group (P = 0.025 for the change between the groups) had metabolic syndrome, which corresponds to an age- and sex-adjusted odds ratio (OR) of 0.62 (95% CI 0.40–0.95) in the intervention group compared with the control group.

The prevalence of different components of metabolic syndrome at year 1 and at the end of the study are shown in Table 1. During the first year, there was a significant decrease in all components except elevated triglycerides in the intervention group, while the control group showed a significant decrease only in the prevalence of elevated blood pressure. From baseline to the end of the study, a significant decrease in the prevalence of abdominal obesity, elevated blood pressure, low HDL cholesterol, and elevated triglycerides was observed in the intervention group, but only low HDL cholesterol was observed in the control group. At the end of the study, between-group comparisons showed that lifestyle intervention reduced abdominal obesity (OR 0.48 [95% CI 0.28–0.81], adjusted for age, sex, and baseline value).


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Table 1— Prevalence of metabolic syndrome and its components in the intervention group (IG) and in the control group (CG) at baseline, at year 1, and at the end of the DPS

 

    CONCLUSIONS—
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
In this secondary analysis of DPS data, we found that after a mean follow-up of 3.9 years, a significant reduction in the prevalence of metabolic syndrome and abdominal obesity were observed in the intervention group compared with that in the control group. These data provide evidence of benefits associated with lifestyle intervention beyond the prevention of diabetes.

The prevalence of metabolic syndrome, abdominal obesity, and elevated blood glucose decreased significantly in the intervention group compared with the control group during the first year, when the intervention was at its most intense. During the subsequent years, there were some relapses, as expected. Nevertheless, by the end of the study, the proportion of subjects with metabolic syndrome and abdominal obesity was still significantly lower in the intervention group. Abdominal obesity and insulin resistance are the main elements of metabolic syndrome (1012). Uusitupa et al. (13) have shown earlier in a subgroup of DPS participants that a change in body weight strongly correlated with a change in insulin sensitivity. No increase in abdominal obesity was observed in the control group, indicating that the limited advice given to individuals in the control group was probably helpful in stopping progression of obesity. Our results were comparable with those of the U.S. Diabetes Prevention Program (DPP) study (9). In the DPP study, a significant increase in metabolic syndrome was observed in the control group; in our study, the prevalence of metabolic syndrome tended to be lower in the control group, indicating that the "mini-intervention" among control group participants had at least some effect on the occurrence of metabolic syndrome.

The significant decrease in elevated fasting glucose concentration observed after the first year deteriorated during the subsequent years. This is not surprising because all individuals had IGT at baseline. Furthermore, the recently updated cutoff point for elevated fasting plasma glucose criteria in metabolic syndrome is 5.6 mmol/l, while the mean fasting glucose at baseline among DPS participants was 6.1 mmol/l. It would apparently be important to find and treat individuals with metabolic syndrome earlier, before IGT has developed.

In summary, compared with the standard care offered to the control group, the intensive and individualized lifestyle intervention in the DPS reduced the occurrence of abdominal obesity and the overall prevalence of metabolic syndrome in the long term. The occurrence of elevated fasting glucose, elevated blood pressure, low HDL cholesterol, and elevated triglycerides did not significantly differ between groups. Since metabolic syndrome is a major risk factor for type 2 diabetes and cardiovascular disease, these results suggest that lifestyle intervention may also reduce the risk of cardiovascular disease in the long run, but a longer follow-up is needed for confirmation.


    Acknowledgments
 
This study was supported by grants from the Finnish Academy (grants 8473/2,298, 40758/5767, 38387/54175, and 46558), the Ministry of Education, the Novo Nordisk Foundation, the Yrjö Jahnsson Foundation, the Juho Vainio Foundation, the Finnish Diabetes Research Foundation, and the competitive research funding of the Pirkanmaa Hospital District and Kuopio University Hospital.


    Footnotes
 
Published ahead of print at http://care.diabetesjournals.org on 9 January 2008. DOI: 10.2337/dc07-1117. Clinical trial reg. no. NCT00518167, clinicaltrials.gov.

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 August 15, 2007. Accepted for publication December 24, 2007.


    References
 TOP
 ABSTRACT
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 

  1. Pan XR, Li GW, Hu YH, Wang JX, Yang WY, An ZX, Hu ZX, Lin J, Xiao JZ, Cao HB, Liu PA, Jiang XG, Jiang YY, Wang JP, Zheng H, Zhang H, Bennett PH, Howard BV: Effects of diet and exercise in preventing NIDDM in people with impaired glucose tolerance: the Da Qing IGT and Diabetes Study. Diabetes Care 20:537–544, 1997[Abstract]
  2. Tuomilehto J, Lindström J, Eriksson JG, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Laakso M, Louheranta A, Rastas M, Salminen V, Aunola S, Cepaitis Z, Moltchanov V, Hakumäki M, Mannelin M, Martikkala V, Sundvall J, Uusitupa M, the Finnish Diabetes Prevention Study Group: Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance. N Engl J Med 344:1343–1350, 2001[Abstract/Free Full Text]
  3. The Diabetes Prevention Program Research Group: Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med 346:393–403, 2002[Abstract/Free Full Text]
  4. Ramachandran A, Snehalatha C, Mary S, Mukesh B, Bhaskar A, Vijay V, the Indian Diabetes Prevention Programme: The Indian Diabetes Prevention Programme shows that lifestyle modification and metformin prevent type 2 diabetes in Asian Indian subjects with impaired glucose tolerance (IDPP-1). Diabetologia 49:289–297, 2006[Medline]
  5. Eriksson J, Lindström J, Valle T, Aunola S, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Laakso M, Lauhkonen M, Lehto P, Lehtonen, Louheranta A, Mannelin M, Martikkala V, Rastas M, Sundvall J, Turpeinen A, Viljanen T, Uusitupa M, Tuomilehto J: Prevention of type II diabetes in subjects with impaired glucose tolerance: the Diabetes Prevention Study (DPS) in Finland. Diabetologia 42:793–801, 1999[Medline]
  6. Lindström J, Louheranta A, Mannelin M, Rastas M, Salminen V, Eriksson J, Uusitupa M, Tuomilehto J, the Finnish Diabetes Prevention Study Group: The Finnish Diabetes Prevention Study (DPS): lifestyle intervention and 3-year results on diet and physical activity. Diabetes Care 26:3230–3236, 2003[Abstract/Free Full Text]
  7. Grundy SM, Cleeman JI, Daniels SR, Donato KA, Eckel RH, Franklin BA, Gordon DJ, Krauss RM, Savage PJ, Smith SC Jr, Spertus JA, Costa F: Diagnosis and management of the metabolic syndrome: an American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement. Circulation 112:2735–2752, 2005[Free Full Text]
  8. Alberti KGM, Zimmet PZ: Definition, diagnosis and classification of diabetes mellitus and its complications. 1. Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 15:539–553, 1998[Medline]
  9. Orchard TJ, Temprosa M, Goldberg R, Haffner S, Ratner R, Marcovina S, Fowler S, the Diabetes Prevention Program Research Group: The effect of metformin and intensive lifestyle intervention on the metabolic syndrome: the Diabetes Prevention Program randomized trial. Ann Intern Med 142:611–619, 2005[Abstract/Free Full Text]
  10. Alberti KGM, Zimmet PZ, Shaw J: Metabolic syndrome—a new world-wide definition. A Concensus Statement from the International Diabetes Federation. Diabet Med 23:469–480, 2006[Medline]
  11. Eckel RH, Grundy SM, Zimmet PZ: The metabolic syndrome. Lancet 365:1415–1428, 2005[Medline]
  12. Palaniappan L, Carnethon MR, Wang Y, Hanley AJG, Fortmann SP, Haffner SM, Wagenknecht L: Predictors of the incident metabolic syndrome in adults: the Insulin Resistance Atherosclerosis Study. Diabetes Care 27:788–793, 2004[Abstract/Free Full Text]
  13. Uusitupa M, Lindi V, Louheranta A, Salopuro T, Lindström J, Tuomilehto J: Long-term improvement in insulin sensitivity by changing lifestyles of people with impaired glucose tolerance: 4-year results from the Finnish Diabetes Prevention Study. Diabetes 52:2532–2538, 2003[Medline]

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This Article
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