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METHODS: A survey of health-related quality of life using the 12-item Short Form (SF-12) of the Medical Outcomes Study Short Form-36 was mailed to patients attending a family medicine clinic. Multiple regression analyses were used to investigate the relationships between scores on the mental and physical components of the SF-12 and body mass index (BMI) while controlling for age, sex, and family income.
RESULTS: Responses were received from 565 subjects (53%). The relationships among BMI and quality of life in the mental and physical domains were nonlinear. Quality of life scores were optimal when BMI was in the range of 20 to 25 kg per m2.
CONCLUSIONS: The National Heart, Lung, and Blood Institute has published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults. Subjects with BMI in the range 18.5 to 24.9 kg per m2 are classified as having normal weight. These observations suggest that achieving a weight in this range will maximize the patient’s subjective sense of well-being.
Obesity is a common condition that is increasing in prevalence. Mokdad and colleagues1 reported that the prevalence of obesity (defined as a body mass index [BMI] Ž30 kg/m2) increased in the United States from 12.0% in 1991 to 17.9% in 1998. Must and colleagues2 found that the prevalence of morbidities such as diabetes, gallbladder disease, and osteoarthritis increased with severity of overweight (BMI >27 and <30) and obesity. The impact of obesity on health-related quality of life has been less well studied than how it affects physical morbidity and mortality.
Le Pen and coworkers3 surveyed a random sample of 500 French subjects with BMI >27 and a control sample of 500 subjects matched for sex, age, and employment status drawn from the nonobese population. Using a short specific quality of life scale and the Medical Outcomes Study Short Form-36 (SF-36),4 it was found that: (1) moderately obese subjects (BMI >27 and <30) did not significantly differ from those in the control group except for physical capacity; and (2) in the group of obese subjects with a BMI Ž30, quality of life seemed to be impaired for 5 of 9 dimensions of the SF-36 compared with the control population, all related to physical consequences of obesity. The study population perceived itself in terms of poor general health.3 No significant difference was observed between the samples for the psychological and social dimensions of the SF-36. Barofsky and colleagues5 also found that pain had a significant impact on the quality of life of obese patients. Fontaine and coworkers6 reported that weight loss was associated with significantly improved scores relative to baseline on the physical functioning, role-physical, general health, vitality, and mental health domains of the SF-36. The largest improvements were with respect to the vitality, general health perception, and role-physical domains.
In most studies of health-related quality of life, obesity has been treated as a dichotomous variable, with the cut point between nonobese and obese persons commonly set at a BMI of 27 kg per m2. This study presents an analysis of the variation of self-reported quality of life in a survey of primary care patients in relation to BMI as a continuous measure.
Methods
A questionnaire was mailed to all patients of the Family Medicine Centre at Mt Sinai Hospital in Toronto who were 45 to 74 years of age and had made at least 3 visits to the clinic during 1996-1997. A modified Dillman method7 was used with an initial mailing followed by a reminder postcard and a second mailing of the questionnaire. An ethics committee at the University of Toronto approved the project. The 103-question survey included the 12-item Short Form of the SF-36 (SF-12) quality of life instrument (QOL),8 in addition to questions about height, weight, and family income. The SF-12 inquires about physical and mental health and permits the computation of 2 summary scales, the physical component scale (PCS-12) and the mental component scale (MCS-12). These scales have been standardized to a mean score of 50 and a standard deviation (SD) of 10 in the general population.
Multiple linear regression models were used to explore the relationships between PCS-12, MCS-12, and BMI. The variables of age, sex, and family income (in 6 categories) were controlled, but health factors such as hypertension and diabetes which are in the causal pathway between BMI and quality of life were deliberately omitted.9 Modern statistical methodology was used to model the shape of the relationships between BMI and quality-of-life measures. To visualize the relationship, a regression smoother (a nonparametric regression function with no prespecified shape) was fitted to the data. S-Plus software10 was used, but this capability is also available in other statistical packages, such as SPSS.11 The result suggested that the relationships between quality of life and BMI were nonlinear. To accommodate the curvilinear shape ([Figure]), BMI was modeled with restricted cubic splines.12 Restricted cubic splines are a method of describing dose-response curves that make no a priori assumptions about the shape of the curve. Cubic polynomials are fitted between prespecified points on the horizontal axis (knots), and restrictions are placed on the resulting curve to ensure a smooth appearance at those knot points.12 Hypothesis testing can be performed to determine whether the nonlinear components of the model significantly improve the fit to the data. BMI was modeled with a 4-knot restricted cubic spline using Harrell’s Design library13 in S-Plus.10
Results
The survey was mailed to 1061 subjects (668 women, 396 men). Responses were received from 564 subjects (53%). [Table 1] shows the distribution of the respondents by age and sex, and the mean values for BMI and scores on the PCS-12 and MCS-12. The mean BMI did not vary with age or sex. Scores on both scales of the SF-12 were higher among men than women.
In performing the statistical analysis it was assumed that although the distribution of BMI or SF-12 scores among respondents and nonrespondents might differ, the relationships among these variables observed in respondents is generalizable. The regression results for the MCS-12 and PCS-12 are shown in [Table 2]. Interestingly, while the mean PCS-12 scores declined with age, there was a significant increase in the MCS-12 scores with age. Men had higher scores than women, but there was no interaction between BMI and sex. Both MCS-12 and PCS-12 scores increased with rising income. After adjusting for age, sex, and income, there were significant nonlinear relationships between MCS-12 and PCS-12 scores and BMI. The figure shows the relationships between QOL scores and BMI adjusted for purposes of illustration to age 60 years and to an income of Ž$80,000 per year. For both scales, there was a peak in QOL scores for BMI values in the range 20 to 25 kg per m2. For the PCS-12, there was a steady decline in QOL from the peak, with a drop of approximately 5 points (SD=0.5) at a BMI of 30 kg per m2. The relative change in MCS-12 scores was less, with no further decline for BMI greater than 30 kg per m2. The wide confidence limits preclude a confident assessment of the shape of the curve for the MCS-12 in the range of BMI greater than 30 kg per m2.
Discussion
The scales on the SF-12 reflect a self-assessment of well-being, pain, limitations, and energy. Self-reported QOL varied with BMI, with a peak in the range of 20 to 25 kg per m2. The PCS-12 scores declined monotonically from the peak with increasing BMI, consistent with reports of bodily pain as a significant comorbidity of obesity.3,5 There was a proportionally smaller decline from the peak in the MCS-12 scores; scores did not continue to decline for those with BMI >30 kg per m2.
In 1998, the National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults.14 On the basis of BMI they use 5 classes of increasing severity consistent with the idea of graded risk. Subjects with a BMI in the range of 18.5 to 24.9 kg per m2 are classified as having normal weight; those with a BMI of 25.0 to 29.9 kg per m2 are classified as preobese; and those with a BMI greater than 30 kg per m2 are assigned to 3 categories of obesity. The upper cutoff point for healthy weight at 25 kg per m2 is consistent with that recommended by a steering committee of the American Institute of Nutrition15 and an expert committee of the World Health Organization.16 Evaluation of a lower cutoff for healthy weight is complex, because the leanest group in a population is a mix of smokers, persons who have lost weight as a result of underlying disease, and persons who have maintained a lean weight by balancing physical activity and caloric intake.17 In this study, the number of subjects (N=23) with a BMI less than 20 kg per m2 was too low to carefully investigate the lower end of the BMI-QOL relationship.
The observations reported here from a survey of primary care patients suggest that achieving a healthy weight as recommended by the NHLBI will maximize the patient’s subjective sense of well-being.
Acknowledgments
Support from a grant from the American Academy of Family Physicians Foundation is gratefully acknowledged.
1. Mokdad AH, Serdula MK, Dietz WH, Bowman BA, Marks JS, Koplan JP. The spread of the obesity epidemic in the United States, 1991-1998. JAMA 1999;282:1519-22.
2. Must A, Spadano J, Coakley EH, Field AE, Colditz GA, Dietz WH. The disease burden associated with overweight and obesity. JAMA 1999;282:1523-29.
3. Le Pen C, Levy E, Loos F, Banzet MN, Basdevant A. “Specific” scale compared with “generic” scale: a double measurement of the quality of life in a French community sample of obese subjects. J Epidemiol Community Health 1998;52:445-50.
4. Ware JE, Jr, Gandek B. Overview of the SF-36 health survey and the international quality of life assessment (IQOLA) project. J Clin Epidemiol 1998;51:903-12.
5. Barofsky I, Fontaine KR, Cheskin LJ. Pain in the obese: impact on health-related quality-of-life. Ann Behav Med 1998;19:408-10.
6. Fontaine KR, Barofsky I, Andersen RE, et al. Impact of weight loss on health-related quality of life. Qual Life Res 1999;8:275-77.
7. Dillman DA. Mail and telephone surveys: the total design method. New York, NY: Wiley; 1978.
8. Ware JJ, Kosinski M, Keller SD. A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity. Med Care 1996;34:220-33.
9. Rothman KJ, Greenland S. Modern epidemiology. 2nd ed. Baltimore, Md: Lippincott Williams & Wilkins; 1998.
10. S-Plus 2000. Seattle, Wash: MathSoft, Inc; 1999.
11. SPSS Chicago, Ill: SPSS Inc; 1999.
12. Harrell FE, Jr., Lee KL, Pollock BG. Regression models in clinical studies: determining relationships between predictors and response. J Natl Cancer Inst 1988;80:1198-202.
13. Azola C, Harrell FE. An introduction to S-Plus and the Hmisc and Design libraries. Charlottesville, Va: University of Virginia School of Medicine; 1999.
14. NHLBI Obesity Task Force. Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults-the evidence report. National Institutes of Health. Obes Res 1998;2:51S-209S.
15. Kuller LH, St Jeor ST, Dwyer J. Report of the American Institute of Nutrition (AIN) Steering Committee on Healthy Weight. Bethesda, Md: American Institute of Nutrition; 1993.
16. WHO. Obesity: preventing and managing the global epidemic: report of a WHO Consultation on Obesity, Geneva, June 3-5, 1997. Geneva, Switzerland: World Health Organization; 1998.
17. Willett WC, Dietz WH, Colditz GA. Guidelines for healthy weight. N Engl J Med 1999;341:427-34.
METHODS: A survey of health-related quality of life using the 12-item Short Form (SF-12) of the Medical Outcomes Study Short Form-36 was mailed to patients attending a family medicine clinic. Multiple regression analyses were used to investigate the relationships between scores on the mental and physical components of the SF-12 and body mass index (BMI) while controlling for age, sex, and family income.
RESULTS: Responses were received from 565 subjects (53%). The relationships among BMI and quality of life in the mental and physical domains were nonlinear. Quality of life scores were optimal when BMI was in the range of 20 to 25 kg per m2.
CONCLUSIONS: The National Heart, Lung, and Blood Institute has published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults. Subjects with BMI in the range 18.5 to 24.9 kg per m2 are classified as having normal weight. These observations suggest that achieving a weight in this range will maximize the patient’s subjective sense of well-being.
Obesity is a common condition that is increasing in prevalence. Mokdad and colleagues1 reported that the prevalence of obesity (defined as a body mass index [BMI] Ž30 kg/m2) increased in the United States from 12.0% in 1991 to 17.9% in 1998. Must and colleagues2 found that the prevalence of morbidities such as diabetes, gallbladder disease, and osteoarthritis increased with severity of overweight (BMI >27 and <30) and obesity. The impact of obesity on health-related quality of life has been less well studied than how it affects physical morbidity and mortality.
Le Pen and coworkers3 surveyed a random sample of 500 French subjects with BMI >27 and a control sample of 500 subjects matched for sex, age, and employment status drawn from the nonobese population. Using a short specific quality of life scale and the Medical Outcomes Study Short Form-36 (SF-36),4 it was found that: (1) moderately obese subjects (BMI >27 and <30) did not significantly differ from those in the control group except for physical capacity; and (2) in the group of obese subjects with a BMI Ž30, quality of life seemed to be impaired for 5 of 9 dimensions of the SF-36 compared with the control population, all related to physical consequences of obesity. The study population perceived itself in terms of poor general health.3 No significant difference was observed between the samples for the psychological and social dimensions of the SF-36. Barofsky and colleagues5 also found that pain had a significant impact on the quality of life of obese patients. Fontaine and coworkers6 reported that weight loss was associated with significantly improved scores relative to baseline on the physical functioning, role-physical, general health, vitality, and mental health domains of the SF-36. The largest improvements were with respect to the vitality, general health perception, and role-physical domains.
In most studies of health-related quality of life, obesity has been treated as a dichotomous variable, with the cut point between nonobese and obese persons commonly set at a BMI of 27 kg per m2. This study presents an analysis of the variation of self-reported quality of life in a survey of primary care patients in relation to BMI as a continuous measure.
Methods
A questionnaire was mailed to all patients of the Family Medicine Centre at Mt Sinai Hospital in Toronto who were 45 to 74 years of age and had made at least 3 visits to the clinic during 1996-1997. A modified Dillman method7 was used with an initial mailing followed by a reminder postcard and a second mailing of the questionnaire. An ethics committee at the University of Toronto approved the project. The 103-question survey included the 12-item Short Form of the SF-36 (SF-12) quality of life instrument (QOL),8 in addition to questions about height, weight, and family income. The SF-12 inquires about physical and mental health and permits the computation of 2 summary scales, the physical component scale (PCS-12) and the mental component scale (MCS-12). These scales have been standardized to a mean score of 50 and a standard deviation (SD) of 10 in the general population.
Multiple linear regression models were used to explore the relationships between PCS-12, MCS-12, and BMI. The variables of age, sex, and family income (in 6 categories) were controlled, but health factors such as hypertension and diabetes which are in the causal pathway between BMI and quality of life were deliberately omitted.9 Modern statistical methodology was used to model the shape of the relationships between BMI and quality-of-life measures. To visualize the relationship, a regression smoother (a nonparametric regression function with no prespecified shape) was fitted to the data. S-Plus software10 was used, but this capability is also available in other statistical packages, such as SPSS.11 The result suggested that the relationships between quality of life and BMI were nonlinear. To accommodate the curvilinear shape ([Figure]), BMI was modeled with restricted cubic splines.12 Restricted cubic splines are a method of describing dose-response curves that make no a priori assumptions about the shape of the curve. Cubic polynomials are fitted between prespecified points on the horizontal axis (knots), and restrictions are placed on the resulting curve to ensure a smooth appearance at those knot points.12 Hypothesis testing can be performed to determine whether the nonlinear components of the model significantly improve the fit to the data. BMI was modeled with a 4-knot restricted cubic spline using Harrell’s Design library13 in S-Plus.10
Results
The survey was mailed to 1061 subjects (668 women, 396 men). Responses were received from 564 subjects (53%). [Table 1] shows the distribution of the respondents by age and sex, and the mean values for BMI and scores on the PCS-12 and MCS-12. The mean BMI did not vary with age or sex. Scores on both scales of the SF-12 were higher among men than women.
In performing the statistical analysis it was assumed that although the distribution of BMI or SF-12 scores among respondents and nonrespondents might differ, the relationships among these variables observed in respondents is generalizable. The regression results for the MCS-12 and PCS-12 are shown in [Table 2]. Interestingly, while the mean PCS-12 scores declined with age, there was a significant increase in the MCS-12 scores with age. Men had higher scores than women, but there was no interaction between BMI and sex. Both MCS-12 and PCS-12 scores increased with rising income. After adjusting for age, sex, and income, there were significant nonlinear relationships between MCS-12 and PCS-12 scores and BMI. The figure shows the relationships between QOL scores and BMI adjusted for purposes of illustration to age 60 years and to an income of Ž$80,000 per year. For both scales, there was a peak in QOL scores for BMI values in the range 20 to 25 kg per m2. For the PCS-12, there was a steady decline in QOL from the peak, with a drop of approximately 5 points (SD=0.5) at a BMI of 30 kg per m2. The relative change in MCS-12 scores was less, with no further decline for BMI greater than 30 kg per m2. The wide confidence limits preclude a confident assessment of the shape of the curve for the MCS-12 in the range of BMI greater than 30 kg per m2.
Discussion
The scales on the SF-12 reflect a self-assessment of well-being, pain, limitations, and energy. Self-reported QOL varied with BMI, with a peak in the range of 20 to 25 kg per m2. The PCS-12 scores declined monotonically from the peak with increasing BMI, consistent with reports of bodily pain as a significant comorbidity of obesity.3,5 There was a proportionally smaller decline from the peak in the MCS-12 scores; scores did not continue to decline for those with BMI >30 kg per m2.
In 1998, the National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults.14 On the basis of BMI they use 5 classes of increasing severity consistent with the idea of graded risk. Subjects with a BMI in the range of 18.5 to 24.9 kg per m2 are classified as having normal weight; those with a BMI of 25.0 to 29.9 kg per m2 are classified as preobese; and those with a BMI greater than 30 kg per m2 are assigned to 3 categories of obesity. The upper cutoff point for healthy weight at 25 kg per m2 is consistent with that recommended by a steering committee of the American Institute of Nutrition15 and an expert committee of the World Health Organization.16 Evaluation of a lower cutoff for healthy weight is complex, because the leanest group in a population is a mix of smokers, persons who have lost weight as a result of underlying disease, and persons who have maintained a lean weight by balancing physical activity and caloric intake.17 In this study, the number of subjects (N=23) with a BMI less than 20 kg per m2 was too low to carefully investigate the lower end of the BMI-QOL relationship.
The observations reported here from a survey of primary care patients suggest that achieving a healthy weight as recommended by the NHLBI will maximize the patient’s subjective sense of well-being.
Acknowledgments
Support from a grant from the American Academy of Family Physicians Foundation is gratefully acknowledged.
METHODS: A survey of health-related quality of life using the 12-item Short Form (SF-12) of the Medical Outcomes Study Short Form-36 was mailed to patients attending a family medicine clinic. Multiple regression analyses were used to investigate the relationships between scores on the mental and physical components of the SF-12 and body mass index (BMI) while controlling for age, sex, and family income.
RESULTS: Responses were received from 565 subjects (53%). The relationships among BMI and quality of life in the mental and physical domains were nonlinear. Quality of life scores were optimal when BMI was in the range of 20 to 25 kg per m2.
CONCLUSIONS: The National Heart, Lung, and Blood Institute has published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults. Subjects with BMI in the range 18.5 to 24.9 kg per m2 are classified as having normal weight. These observations suggest that achieving a weight in this range will maximize the patient’s subjective sense of well-being.
Obesity is a common condition that is increasing in prevalence. Mokdad and colleagues1 reported that the prevalence of obesity (defined as a body mass index [BMI] Ž30 kg/m2) increased in the United States from 12.0% in 1991 to 17.9% in 1998. Must and colleagues2 found that the prevalence of morbidities such as diabetes, gallbladder disease, and osteoarthritis increased with severity of overweight (BMI >27 and <30) and obesity. The impact of obesity on health-related quality of life has been less well studied than how it affects physical morbidity and mortality.
Le Pen and coworkers3 surveyed a random sample of 500 French subjects with BMI >27 and a control sample of 500 subjects matched for sex, age, and employment status drawn from the nonobese population. Using a short specific quality of life scale and the Medical Outcomes Study Short Form-36 (SF-36),4 it was found that: (1) moderately obese subjects (BMI >27 and <30) did not significantly differ from those in the control group except for physical capacity; and (2) in the group of obese subjects with a BMI Ž30, quality of life seemed to be impaired for 5 of 9 dimensions of the SF-36 compared with the control population, all related to physical consequences of obesity. The study population perceived itself in terms of poor general health.3 No significant difference was observed between the samples for the psychological and social dimensions of the SF-36. Barofsky and colleagues5 also found that pain had a significant impact on the quality of life of obese patients. Fontaine and coworkers6 reported that weight loss was associated with significantly improved scores relative to baseline on the physical functioning, role-physical, general health, vitality, and mental health domains of the SF-36. The largest improvements were with respect to the vitality, general health perception, and role-physical domains.
In most studies of health-related quality of life, obesity has been treated as a dichotomous variable, with the cut point between nonobese and obese persons commonly set at a BMI of 27 kg per m2. This study presents an analysis of the variation of self-reported quality of life in a survey of primary care patients in relation to BMI as a continuous measure.
Methods
A questionnaire was mailed to all patients of the Family Medicine Centre at Mt Sinai Hospital in Toronto who were 45 to 74 years of age and had made at least 3 visits to the clinic during 1996-1997. A modified Dillman method7 was used with an initial mailing followed by a reminder postcard and a second mailing of the questionnaire. An ethics committee at the University of Toronto approved the project. The 103-question survey included the 12-item Short Form of the SF-36 (SF-12) quality of life instrument (QOL),8 in addition to questions about height, weight, and family income. The SF-12 inquires about physical and mental health and permits the computation of 2 summary scales, the physical component scale (PCS-12) and the mental component scale (MCS-12). These scales have been standardized to a mean score of 50 and a standard deviation (SD) of 10 in the general population.
Multiple linear regression models were used to explore the relationships between PCS-12, MCS-12, and BMI. The variables of age, sex, and family income (in 6 categories) were controlled, but health factors such as hypertension and diabetes which are in the causal pathway between BMI and quality of life were deliberately omitted.9 Modern statistical methodology was used to model the shape of the relationships between BMI and quality-of-life measures. To visualize the relationship, a regression smoother (a nonparametric regression function with no prespecified shape) was fitted to the data. S-Plus software10 was used, but this capability is also available in other statistical packages, such as SPSS.11 The result suggested that the relationships between quality of life and BMI were nonlinear. To accommodate the curvilinear shape ([Figure]), BMI was modeled with restricted cubic splines.12 Restricted cubic splines are a method of describing dose-response curves that make no a priori assumptions about the shape of the curve. Cubic polynomials are fitted between prespecified points on the horizontal axis (knots), and restrictions are placed on the resulting curve to ensure a smooth appearance at those knot points.12 Hypothesis testing can be performed to determine whether the nonlinear components of the model significantly improve the fit to the data. BMI was modeled with a 4-knot restricted cubic spline using Harrell’s Design library13 in S-Plus.10
Results
The survey was mailed to 1061 subjects (668 women, 396 men). Responses were received from 564 subjects (53%). [Table 1] shows the distribution of the respondents by age and sex, and the mean values for BMI and scores on the PCS-12 and MCS-12. The mean BMI did not vary with age or sex. Scores on both scales of the SF-12 were higher among men than women.
In performing the statistical analysis it was assumed that although the distribution of BMI or SF-12 scores among respondents and nonrespondents might differ, the relationships among these variables observed in respondents is generalizable. The regression results for the MCS-12 and PCS-12 are shown in [Table 2]. Interestingly, while the mean PCS-12 scores declined with age, there was a significant increase in the MCS-12 scores with age. Men had higher scores than women, but there was no interaction between BMI and sex. Both MCS-12 and PCS-12 scores increased with rising income. After adjusting for age, sex, and income, there were significant nonlinear relationships between MCS-12 and PCS-12 scores and BMI. The figure shows the relationships between QOL scores and BMI adjusted for purposes of illustration to age 60 years and to an income of Ž$80,000 per year. For both scales, there was a peak in QOL scores for BMI values in the range 20 to 25 kg per m2. For the PCS-12, there was a steady decline in QOL from the peak, with a drop of approximately 5 points (SD=0.5) at a BMI of 30 kg per m2. The relative change in MCS-12 scores was less, with no further decline for BMI greater than 30 kg per m2. The wide confidence limits preclude a confident assessment of the shape of the curve for the MCS-12 in the range of BMI greater than 30 kg per m2.
Discussion
The scales on the SF-12 reflect a self-assessment of well-being, pain, limitations, and energy. Self-reported QOL varied with BMI, with a peak in the range of 20 to 25 kg per m2. The PCS-12 scores declined monotonically from the peak with increasing BMI, consistent with reports of bodily pain as a significant comorbidity of obesity.3,5 There was a proportionally smaller decline from the peak in the MCS-12 scores; scores did not continue to decline for those with BMI >30 kg per m2.
In 1998, the National Heart, Lung, and Blood Institute (NHLBI) of the National Institutes of Health published evidence-based clinical guidelines for the identification, evaluation, and treatment of overweight and obesity in adults.14 On the basis of BMI they use 5 classes of increasing severity consistent with the idea of graded risk. Subjects with a BMI in the range of 18.5 to 24.9 kg per m2 are classified as having normal weight; those with a BMI of 25.0 to 29.9 kg per m2 are classified as preobese; and those with a BMI greater than 30 kg per m2 are assigned to 3 categories of obesity. The upper cutoff point for healthy weight at 25 kg per m2 is consistent with that recommended by a steering committee of the American Institute of Nutrition15 and an expert committee of the World Health Organization.16 Evaluation of a lower cutoff for healthy weight is complex, because the leanest group in a population is a mix of smokers, persons who have lost weight as a result of underlying disease, and persons who have maintained a lean weight by balancing physical activity and caloric intake.17 In this study, the number of subjects (N=23) with a BMI less than 20 kg per m2 was too low to carefully investigate the lower end of the BMI-QOL relationship.
The observations reported here from a survey of primary care patients suggest that achieving a healthy weight as recommended by the NHLBI will maximize the patient’s subjective sense of well-being.
Acknowledgments
Support from a grant from the American Academy of Family Physicians Foundation is gratefully acknowledged.
1. Mokdad AH, Serdula MK, Dietz WH, Bowman BA, Marks JS, Koplan JP. The spread of the obesity epidemic in the United States, 1991-1998. JAMA 1999;282:1519-22.
2. Must A, Spadano J, Coakley EH, Field AE, Colditz GA, Dietz WH. The disease burden associated with overweight and obesity. JAMA 1999;282:1523-29.
3. Le Pen C, Levy E, Loos F, Banzet MN, Basdevant A. “Specific” scale compared with “generic” scale: a double measurement of the quality of life in a French community sample of obese subjects. J Epidemiol Community Health 1998;52:445-50.
4. Ware JE, Jr, Gandek B. Overview of the SF-36 health survey and the international quality of life assessment (IQOLA) project. J Clin Epidemiol 1998;51:903-12.
5. Barofsky I, Fontaine KR, Cheskin LJ. Pain in the obese: impact on health-related quality-of-life. Ann Behav Med 1998;19:408-10.
6. Fontaine KR, Barofsky I, Andersen RE, et al. Impact of weight loss on health-related quality of life. Qual Life Res 1999;8:275-77.
7. Dillman DA. Mail and telephone surveys: the total design method. New York, NY: Wiley; 1978.
8. Ware JJ, Kosinski M, Keller SD. A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity. Med Care 1996;34:220-33.
9. Rothman KJ, Greenland S. Modern epidemiology. 2nd ed. Baltimore, Md: Lippincott Williams & Wilkins; 1998.
10. S-Plus 2000. Seattle, Wash: MathSoft, Inc; 1999.
11. SPSS Chicago, Ill: SPSS Inc; 1999.
12. Harrell FE, Jr., Lee KL, Pollock BG. Regression models in clinical studies: determining relationships between predictors and response. J Natl Cancer Inst 1988;80:1198-202.
13. Azola C, Harrell FE. An introduction to S-Plus and the Hmisc and Design libraries. Charlottesville, Va: University of Virginia School of Medicine; 1999.
14. NHLBI Obesity Task Force. Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults-the evidence report. National Institutes of Health. Obes Res 1998;2:51S-209S.
15. Kuller LH, St Jeor ST, Dwyer J. Report of the American Institute of Nutrition (AIN) Steering Committee on Healthy Weight. Bethesda, Md: American Institute of Nutrition; 1993.
16. WHO. Obesity: preventing and managing the global epidemic: report of a WHO Consultation on Obesity, Geneva, June 3-5, 1997. Geneva, Switzerland: World Health Organization; 1998.
17. Willett WC, Dietz WH, Colditz GA. Guidelines for healthy weight. N Engl J Med 1999;341:427-34.
1. Mokdad AH, Serdula MK, Dietz WH, Bowman BA, Marks JS, Koplan JP. The spread of the obesity epidemic in the United States, 1991-1998. JAMA 1999;282:1519-22.
2. Must A, Spadano J, Coakley EH, Field AE, Colditz GA, Dietz WH. The disease burden associated with overweight and obesity. JAMA 1999;282:1523-29.
3. Le Pen C, Levy E, Loos F, Banzet MN, Basdevant A. “Specific” scale compared with “generic” scale: a double measurement of the quality of life in a French community sample of obese subjects. J Epidemiol Community Health 1998;52:445-50.
4. Ware JE, Jr, Gandek B. Overview of the SF-36 health survey and the international quality of life assessment (IQOLA) project. J Clin Epidemiol 1998;51:903-12.
5. Barofsky I, Fontaine KR, Cheskin LJ. Pain in the obese: impact on health-related quality-of-life. Ann Behav Med 1998;19:408-10.
6. Fontaine KR, Barofsky I, Andersen RE, et al. Impact of weight loss on health-related quality of life. Qual Life Res 1999;8:275-77.
7. Dillman DA. Mail and telephone surveys: the total design method. New York, NY: Wiley; 1978.
8. Ware JJ, Kosinski M, Keller SD. A 12-item short-form health survey: construction of scales and preliminary tests of reliability and validity. Med Care 1996;34:220-33.
9. Rothman KJ, Greenland S. Modern epidemiology. 2nd ed. Baltimore, Md: Lippincott Williams & Wilkins; 1998.
10. S-Plus 2000. Seattle, Wash: MathSoft, Inc; 1999.
11. SPSS Chicago, Ill: SPSS Inc; 1999.
12. Harrell FE, Jr., Lee KL, Pollock BG. Regression models in clinical studies: determining relationships between predictors and response. J Natl Cancer Inst 1988;80:1198-202.
13. Azola C, Harrell FE. An introduction to S-Plus and the Hmisc and Design libraries. Charlottesville, Va: University of Virginia School of Medicine; 1999.
14. NHLBI Obesity Task Force. Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults-the evidence report. National Institutes of Health. Obes Res 1998;2:51S-209S.
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