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Published online December 10, 2007
Diabetes Care 31:583-584, 2008
DOI: 10.2337/dc07-1390
© 2008 by the American Diabetes Association
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Cardiovascular and Metabolic Risk
Original Research

Underweight as a Predictor of Diabetes in Older Adults

A large cohort study

Toshimi Sairenchi, PHD1,2, Hiroyasu Iso, MD, PHD, MPH3, Fujiko Irie, MD, PHD4, Nobuko Fukasawa, PHN2, Hitoshi Ota, MD, PHD1 and Takashi Muto, MD, PHD1

1 Department of Public Health, Dokkyo Medical University School of Medicine, Tochigi-ken, Japan
2 Ibaraki Prefectural Health Plaza, Ibaraki-ken, Japan
3 Public Health, Department of Social and Environmental Medicine, Osaka University Graduate School of Medicine, Osaka-fu, Japan
4 Department of Health and Welfare, Ibaraki Prefectural Office, Ibaraki-ken, Japan

Address correspondence and reprint requests to Toshimi Sairenchi, PhD, Dokkyo Medical University, 880 Kita-kobayashi, Mibu, Tochigi, 321-0293, Japan. E-mail: tossair{at}dokkyomed.ac.jp


    INTRODUCTION
 TOP
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
A total of 39,201 men and 88,012 women aged 40–79 years who underwent health checkups in 1993 and who were free of diabetes were followed until the end of 2004 to examine an association between underweight and risk of diabetes. Incident diabetes was defined by a fasting blood glucose concentration ≥7.0 mmol/l or nonfasting glucose ≥11.1 mmol/l and/or diabetes treatment. The multivariable hazard ratio of diabetes adjusted for age, baseline blood glucose level, fasting status, and other confounding variables among subjects who had a BMI <18.5 kg/m2 compared with those with a BMI 18.5–24.9 kg/m2 was 1.32 (95% CI 1.12–1.56) in men aged 60–79 years and 1.31 (1.07–1.60) in women aged 60–79 years. Underweight may be associated with risk of diabetes among older adults.


    RESEARCH DESIGN AND METHODS—
 TOP
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
In the present study, we enrolled 181,863 nondiabetic Japanese subjects (58,402 men and 123,461 women) from community residents aged 40–79 years who underwent health checkups in 1993 conducted by the local governments under the Japan Health Laws. We excluded 19,201 men and 35,449 women who did not participate in the 1994 survey, thereby ensuring that the subjects were followed up for at least 1 year. A total of 39,201 men and 88,012 women were followed up annually until the diagnosis of diabetes mellitus or the end of 2004. Individuals who did not undergo checkups during the follow-up periods were censored on the date of their latest checkup.

At baseline in 1993, height and weight were measured. BMI was calculated as weight in kilograms divided by the square of height in meters. Plasma glucose, serum total cholesterol, triglyceride, and HDL cholesterol were measured. An interview was conducted to ascertain smoking status (never smoked; exsmoker; current smoker, <20 cigarettes per day; and current smoker, ≥20 cigarettes perday) and alcohol intake (never, sometimes, <66 g/day, and ≥66 g/day).

We diagnosed incidence of diabetes when there was a fasting plasma glucose level ≥7.0 mmol/l or a nonfasting plasma glucose level ≥11.1 mmol/l and/or when a person had begun to receive treatment for diabetes. Fasting was defined as not having had a meal for at least 8 h.

HRs for diabetes according to BMI (<18.5, 18.5–24.9, and ≥30.0 kg/m2) were calculated using a multivariable Cox proportional hazards regression model. Covariates included age (years), baseline blood glucose level (millimoles per liter), fasting status (yes or no), antihypertensive medication use (yes or no), antihyperlipidemic medication use (yes or no), serum total cholesterol level (millimoles per liter), serum HDL cholesterol level (millimoles per liter), log-transformed triglyceride level (millimoles per liter), systolic blood pressure level, smoking status (never smoked; exsmoker; current smoker, <20 cigarettes per day; and current smoker, ≥20 cigarettes per day), and alcohol intake (never, sometimes, <66 g/day, and ≥66 g/day).


    RESULTS—
 TOP
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
Of the 127,213 subjects (39,201 men and 88,012 women), 8,447 developed diabetes (3,863 men and 4,584 women) during a mean of 5.3 years of follow-up (4.9 years for men and 5.4 years for women).

Table 1 shows age-specific HRs of diabetes according to BMI. Compared with subjects with BMI 18.5–24.9 kg/m2, the multivariable HR for diabetes among subjects with BMI <18.5 kg/m2 (underweight) was 1.32 (95% CI 1.12–1.56) in men aged 60–79 years and 1.31 (1.07–1.60) in women aged 60–79 years. No significant association was found between underweight and risk of diabetes in either sex aged 40–59 years.


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Table 1— Age-specific HRs (95% CIs) for incidence of diabetes according to BMI among 39,201 men and 88,012 women in Ibaraki-ken, Japan, 1993–2004

 
The interaction between age-group and underweight versus BMI 18.5–24.9 kg/m2 was statistically significant for women (P = 0.012) but not men (P = 0.800).


    CONCLUSIONS—
 TOP
 INTRODUCTION
 RESEARCH DESIGN AND METHODS--
 RESULTS--
 CONCLUSIONS--
 References
 
To our knowledge, this is the first prospective large-cohort study to show significant associations of low and high BMI with risks of diabetes among older adults. Mechanisms behind the association between low BMI (underweight) and diabetes among older adults are uncertain. Insulin secretion declines in older adults (1); and lean diabetic older adults exhibit a profound impairment in glucose-induced insulin release while obese diabetic older adults do not (2). Several experimental studies using rats showed that protein-calorie malnutrition and magnesium deficiency cause low insulin secretion and a low pancreatic insulin store (3,4). In humans, a study of 556 older adult subjects reported that a poor nutritional status was associated with the prevalence of type 2 diabetes; mean serum albumin levels were lower among diabetic than nondiabetic subjects (5). Furthermore, low dietary magnesium was associated with risk of type 2 diabetes (6).

The strength of the present study comes from the use of a large cohort in which the incidence of diabetes was ascertained by blood glucose levels, as opposed to many previous large-cohort studies by self-administered questionnaire (7,8). On the other hand, our study had several limitations. First, potential confounding factors brought about by physical activity remained because we did not assess this variable. However, physical activity was reported to not substantially alter the association between BMI and risk of diabetes (9). Second, oral glucose tolerance tests were not conducted for diagnosis of diabetes. Third, the follow-up rate was moderate. However, the BMI distributions were similar between the subjects followed and those not followed. Therefore, the results were unlikely to be affected by the participants not followed. Fourth, although we addressed the association between underweight and excess risk of diabetes among older adults, the magnitude of the relationship for whole population might be small because large sample size yields excess statistical power. Finally, the subjects in the present study were residents of only a single prefecture in Japan. In summary, underweight may be associated with risk of diabetes among older adults.


    Footnotes
 
Published ahead of print at http://care.diabetesjournals.org on 10 December 2007. DOI: 10.2337/dc07-1390.

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 July 19, 2007. Accepted for publication November 28, 2007.


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

  1. Basu R, Breda E, Oberg AL, Powell CC, Dalla Man C, Basu A, Vittone JL, Klee GG, Arora P, Jensen MD, Toffolo G, Cobelli C, Rizza RA: Mechanisms of the age-associated deterioration in glucose tolerance: contribution of alterations in insulin secretion, action, and clearance. Diabetes 52:1738–1748, 2003[Medline]
  2. Meneilly GS, Elliott T, Tessier D, Hards L, Tildesley H: NIDDM in the elderly. Diabetes Care 19:1320–1325, 1996[Abstract]
  3. Legrand C, Okitolonda W, Pottier AM, Lederer J, Henquin JC: Glucose homeostasis in magnesium-deficient rats. Metabolism 36:160–164, 1987[Medline]
  4. Okitolonda W, Brichard SM, Henquin JC: Repercussions of chronic protein-calorie malnutrition on glucose homeostasis in the rat. Diabetologia 30:946–951, 1987[Medline]
  5. Castaneda C, Bermudez OI, Tucker KL: Protein nutritional status and function are associated with type 2 diabetes in Hispanic elders. Am J Clin Nutr 72:89–95, 2000[Abstract/Free Full Text]
  6. Lopez-Ridaura R, Willett WC, Rimm EB, Liu S, Stampfer MJ, Manson JE, Hu FB: Magnesium intake and risk of type 2 diabetes in men and women. Diabetes Care 27:134–140, 2004[Abstract/Free Full Text]
  7. Colditz GA, Willett WC, Stampfer MJ, Manson JE, Hennekens CH, Arky RA, Speizer FE: Weight as a risk factor for clinical diabetes in women. Am J Epidemiol 132:501–513, 1990[Abstract/Free Full Text]
  8. Chan JM, Rimm EB, Colditz GA, Stampfer MJ, Willett WC: Obesity, fat distribution, and weight gain as risk factors for clinical diabetes in men. Diabetes Care 17:961–969, 1994[Abstract]
  9. Weinstein AR, Sesso HD, Lee IM, Cook NR, Manson JE, Buring JE, Gaziano JM: Relationship of physical activity vs. body mass index with type 2 diabetes in women. JAMA 292:1188–1194, 2004[Abstract/Free Full Text]

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This Article
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