[Skip to Navigation]
Sign In
Figure 1. 
The unadjusted association of smoking status and the number of cigarettes smoked daily at baseline in 1974 and mortality during the 26-year follow-up period. Arrows indicate the difference of survival in years between never-smokers and participants who smoked more than 20 cigarettes daily; vertical dotted line, survival to 73 years, the mean age at follow-up.

The unadjusted association of smoking status and the number of cigarettes smoked daily at baseline in 1974 and mortality during the 26-year follow-up period. Arrows indicate the difference of survival in years between never-smokers and participants who smoked more than 20 cigarettes daily; vertical dotted line, survival to 73 years, the mean age at follow-up.

Figure 2. 
The age-adjusted association of smoking status at baseline in 1974 and health-related quality of life as RAND 36-Item Health Survey (RAND-36) scores in 2000. BP indicates bodily pain; GH, general health; MH, mental health/emotional well-being; PF, physical functioning; RE, role limitations owing to mental problems; RP, role limitations owing to physical health; SF, social functioning; and VT, energy/vitality.

The age-adjusted association of smoking status at baseline in 1974 and health-related quality of life as RAND 36-Item Health Survey (RAND-36) scores in 2000. BP indicates bodily pain; GH, general health; MH, mental health/emotional well-being; PF, physical functioning; RE, role limitations owing to mental problems; RP, role limitations owing to physical health; SF, social functioning; and VT, energy/vitality.

Figure 3. 
The age-adjusted association of smoking status at baseline in 1974 and health-related quality of life as RAND 36-Item Health Survey (RAND-36) physical (PCS) and mental (MCS) component summary scores in 2000.

The age-adjusted association of smoking status at baseline in 1974 and health-related quality of life as RAND 36-Item Health Survey (RAND-36) physical (PCS) and mental (MCS) component summary scores in 2000.

Table. 
Baseline Characteristics of 1658 Participants According to Smoking Status in 1974a
Baseline Characteristics of 1658 Participants According to Smoking Status in 1974a
1.
Doll  RPeto  RBoreham  JSutherland  I Mortality in relation to smoking: 50 years' observations on male British doctors.  BMJ 2004;328 (7455) 1519- 1533PubMedGoogle Scholar
2.
Brønnum-Hansen  HJuel  K Abstention from smoking extends life and compresses morbidity: a population-based study of health expectancy among smokers and never smokers in Denmark.  Tob Control 2001;10 (3) 273- 278PubMedGoogle Scholar
3.
Martel  LBelanger  ABerthelot  J Smoking and disability-free life expectancy in Canada. Bélanger  ACarrière  YGilbert  S Report on the Demographic Situation in Canada. Ottawa, Quebec, Canada Statistics Canada, Demography Division2000;111- 134Google Scholar
4.
Rogers  RGPowell-Griner  E Life expectancies of cigarette smokers and nonsmokers in the United States.  Soc Sci Med 1991;32 (10) 1151- 1159PubMedGoogle Scholar
5.
Dallongeville  JMarecaux  NFruchart  JC  et al.  Cigarette smoking is associated with unhealthy patterns of nutrient intake: a meta-analysis.  J Nutr 1998;128 (9) 1450- 1457PubMedGoogle Scholar
6.
Jarvis  MWardle  J Social patterning of individual health behaviours: the case of cigarette smoking. Marmot  MWilkinson  R Social Determinants of Health. Oxford, England Oxford University Press1999;240- 255Google Scholar
7.
Mamun  AAPeeters  ABarendregt  JWillekens  FNusselder  WBonneux  L Smoking decreases the duration of life lived with and without cardiovascular disease: a life course analysis of the Framingham Heart Study.  Eur Heart J 2004;25 (5) 409- 415PubMedGoogle Scholar
8.
Guralnik  JMKaplan  GA Predictors of healthy aging: prospective evidence from the Alameda County study.  Am J Public Health 1989;79 (6) 703- 708PubMedGoogle Scholar
9.
Ebrahim  SWannamethee  SGWhincup  PWalker  MShaper  AG Locomotor disability in a cohort of British men: the impact of lifestyle and disease.  Int J Epidemiol 2000;29 (3) 478- 486PubMedGoogle Scholar
10.
Miettinen  TAHuttunen  JKNaukkarinen  V  et al.  Multifactorial primary prevention of cardiovascular diseases in middle-aged men: risk factor changes, incidence, and mortality.  JAMA 1985;254 (15) 2097- 2102PubMedGoogle Scholar
11.
Hays  RDMorales  LS The RAND-36 measure of health-related quality of life.  Ann Med 2001;33 (5) 350- 357PubMedGoogle Scholar
12.
Garratt  ASchmidt  LMackintosh  AFitzpatrick  R Quality of life measurement: bibliographic study of patient assessed health outcome measures.  BMJ 2002;324 (7351) 1417- 1422PubMedGoogle Scholar
13.
Haywood  KLGarratt  AMFitzpatrick  R Quality of life in older people: a structured review of generic self-assessed health instruments.  Qual Life Res 2005;14 (7) 1651- 1668PubMedGoogle Scholar
14.
Aalto  A-MAro  ARTeperi  J RAND-36 as a Measure of Health-Related Quality of Life: Reliability, Construct Validity, and Reference Values in the Finnish General Population.  Helsinki, Finland STAKES1999;STAKES Research Report 101
15.
Ware  JEKosinski  M SF-36 Physical and Mental Health Summary Scales: A Manual for Users of Version 1. 2nd ed. Lincoln, RI QualityMetric Inc2001;
16.
Dubuc  NHaley  SMNi  PKooyoomjian  JTJette  AM Function and disability in late life: comparison of the Late-Life Function and Disability Instrument to the Short-Form-36 and the London Handicap Scale.  Disabil Rehabil 2004;26 (6) 362- 370Google Scholar
17.
Daviglus  MLLiu  KPirzada  A  et al.  Favorable cardiovascular risk profile in middle age and health-related quality of life in older age.  Arch Intern Med 2003;163 (20) 2460- 2468PubMedGoogle Scholar
18.
Strandberg  AStrandberg  TESalomaa  VVPitkälä  KHappola  OMiettinen  TA A follow-up study found that cardiovascular risk in middle age predicted mortality and quality of life in old age.  J Clin Epidemiol 2004;57 (4) 415- 421PubMedGoogle Scholar
19.
Tillmann  MSilcock  J A comparison of smokers' and ex-smokers' health-related quality of life.  J Public Health Med 1997;19 (3) 268- 273PubMedGoogle Scholar
20.
Lyons  RALo  SVLittlepage  BNC Perception of health amongst ever-smokers and never-smokers: a comparison using the SF-36 Health Survey Questionnaire.  Tob Control 1994;3213- 21510.1136/tc.3.3.213Google Scholar
21.
Mody  RRSmith  MJ Smoking status and health-related quality of life: as findings from the 2001 Behavioral Risk Factor Surveillance System data.  Am J Health Promot 2006;20 (4) 251- 258PubMedGoogle Scholar
22.
Wilson  DParsons  JWakefield  M The health-related quality-of-life of never smokers, ex-smokers, and light, moderate, and heavy smokers.  Prev Med 1999;29 (3) 139- 144PubMedGoogle Scholar
23.
Taira  DASeto  TBHo  KK  et al.  Impact of smoking on health-related quality of life after percutaneous coronary revascularization.  Circulation 2000;102 (12) 1369- 1374PubMedGoogle Scholar
24.
Turner  JPage-Shafer  KChin  DP  et al.  Adverse impact of cigarette smoking on dimensions of health-related quality of life in persons with HIV infection.  AIDS Patient Care STDS 2001;15 (12) 615- 624PubMedGoogle Scholar
25.
Garces  YIYang  PParkinson  J  et al.  The relationship between cigarette smoking and quality of life after lung cancer diagnosis.  Chest 2004;126 (6) 1733- 1741PubMedGoogle Scholar
26.
Østbye  TTaylor  DH The effect of smoking on years of healthy life (YHL) lost among middle-aged and older Americans.  Health Serv Res 2004;39 (3) 531- 552PubMedGoogle Scholar
27.
Thorn  JBjorkelund  CBengtsson  CGuo  XLissner  LSundh  V Low socio-economic status, smoking, mental stress and obesity predict obstructive symptoms in women, but only smoking also predicts subsequent experience of poor health.  Int J Med Sci 2007;4 (1) 7- 12PubMedGoogle Scholar
28.
Croghan  ITSchroeder  DRHays  JT  et al.  Nicotine dependence treatment: perceived health status improvement with 1-year continuous smoking abstinence.  Eur J Public Health 2005;15 (3) 251- 255PubMedGoogle Scholar
29.
Mitra  MChung  MCWilber  NKlein Walker  D Smoking status and quality of life: a longitudinal study among adults with disabilities.  Am J Prev Med 2004;27 (3) 258- 260PubMedGoogle Scholar
30.
Goddard  E Smoking and Drinking Among Adults, 2005.  London, England Office for National Statistics2006;General Household Survey 2005
31.
 The 1991 National Household Survey on Drug Abuse.  Research Triangle Park, NC Research Triangle Institute1991; Preventing Tobacco Use Among Young People: A Report of the Surgeon General US. Atlanta, GA Dept of Health and Human Services1994;Google Scholar
32.
Diehr  PJohnson  LL Accounting for missing data in end-of-life research.  J Palliat Med 2005;8 ((suppl 1)) S50- S57PubMedGoogle Scholar
33.
 Tobacco Statistics 2005.  Helsinki, Finland Statistics Finland2006;Official Statistics of Finland, Health 2006 Report Series
34.
Martinez  JAMota  GAVianna  ESFilho  JTSilva  GARodrigues  AL  Jr Impaired quality of life of healthy young smokers.  Chest 2004;125 (2) 425- 428PubMedGoogle Scholar
35.
Chandola  TFerrie  JSacker  AMarmot  M Social inequalities in self reported health in early old age: follow-up of prospective cohort study.  BMJ 2007;334 (7601) 990- 997PubMedGoogle Scholar
36.
Fries  JFGreen  LWLevine  S Health promotion and the compression of morbidity.  Lancet 1989;1 (8636) 481- 483PubMedGoogle Scholar
37.
Nusselder  WJLooman  CWNMarang–van de Mheen  PJvan de Mheen  HMackenbach  JP Smoking and the compression of morbidity.  J Epidemiol Community Health 2000;54 (8) 566- 574PubMedGoogle Scholar
Original Investigation
October 13, 2008

The Effect of Smoking in Midlife on Health-Related Quality of Life in Old Age: A 26-Year Prospective Study

Author Affiliations

Author Affiliations: Geriatric Clinic, Department of Medicine, University of Helsinki (Drs A. Y. Strandberg, Pitkälä, Tilvis, and Miettinen), and National Public Health Institute (Dr Salomaa), Helsinki, Finland; and Department of Health Sciences/Geriatrics, University of Oulu, and Unit of General Practice, Oulu University Hospital, Oulu, Finland (Dr T. E. Strandberg).

Arch Intern Med. 2008;168(18):1968-1974. doi:10.1001/archinte.168.18.1968
Abstract

Background  Smoking shortens life expectancy by 7 to 10 years. However, it is unclear whether the enhanced longevity of nonsmokers produces increased disability and decreased quality of life during these extra final years. This study evaluates the long-term effect of smoking in midlife on health-related quality of life (HRQoL) in old age.

Methods  Prospective cohort study with a 26-year follow-up of 1658 white men (born 1919-1934) of similar socioeconomic status who were participating in the Helsinki Businessmen Study. All men were healthy at baseline in 1974, when cardiovascular risk factors and smoking habits were assessed. The participants were reevaluated with the use of mailed questionnaires in 2000; HRQoL was measured with the use of the RAND 36-Item Health Survey (similar to the Medical Outcomes Study Short-Form Health Survey) and related to the baseline smoking status. Total mortality through 2000 was determined from Finnish national registers.

Results  Participants who had never smoked (n = 614) lived a mean of 10 years longer than heavy smokers (>20 cigarettes daily; n = 188). Among survivors in 2000 (n = 1131), the never-smokers had the highest (ie, best) scores on all RAND 36-Item Health Survey scales. The differences were greatest between never-smokers and heavy smokers, ranging from 4 points on the scale of social functioning to 14 points on the physical functioning scale. The physical component summary score showed a graded deterioration of HRQoL with an increasing number of cigarettes smoked daily (P = .01).

Conclusions  During the 26-year follow-up of this socioeconomically homogeneous male cohort, HRQoL deteriorated with an increase in daily cigarettes smoked in a dose-dependent manner. Never-smokers lived longer than heavy smokers, and their extra years were of better quality.

Numerous studies have demonstrated the various ill effects that the use of tobacco has on health, particularly by causing vascular, neoplastic, and respiratory tract diseases. Among men, smoking has been shown to shorten life by 7 to 10 years.1-4 In addition to increased morbidity, smoking is also linked to factors that may affect quality of life, such as poorer nutrition5 or lower socioeconomic status.6

Therefore, it is plausible that smoking also diminishes health-related quality of life (HRQoL) in the long term. However, dying earlier does not necessarily mean worse HRQoL, especially during the last years of life. Living longer may produce more years of disability and lower HRQoL during the achieved extra years. If nonsmokers live longer, then they also have more time to develop coronary heart disease or other chronic diseases that cause disability and worse HRQoL.7 On the other hand, nonsmokers have been shown to have less disability.8,9

Thus, it is not clear whether the additional final years gained by not smoking are also better in quality. Are smokers right when they defend their habit by declaring they prefer a merrier, albeit a shorter, life? This can only be investigated in a long-term follow-up study that begins before smoking has had its negative health effects and with a follow-up time long enough to enable measuring HRQoL during participants' final years. The relationship between long-term smoking and HRQoL has not previously been studied under these circumstances.

Methods
Baseline examination

In a longitudinal study, a cohort of originally healthy Finnish men was prospectively observed from 1964 through the 2000s and assessed for cardiovascular risk factors, mortality, morbidity, and quality of life. All participants were white businessmen or executives with similar socioeconomic and job status. Mean (SD) age in 1974 was 47.8 (4.1) years. The study population and methods have been described in detail elsewhere.10 This study was approved by the local ethics committee.

For this study, we analyzed the effect of smoking status in 1974 on mortality and HRQoL in 2000. In 1974, detailed smoking status was available for 2464 men. Of these, we excluded 581 men with any chronic disease or who were taking regular prescription medication and 160 men who reported smoking cigars or pipes. Therefore, all 1658 men included in this study were healthy, professionally active in positions of responsibility, and did not take regular medication or have signs of chronic diseases, including diabetes mellitus, cardiovascular disease, malignant neoplasms, psychiatric disorders, or alcoholism.

During baseline examinations, weight and height were measured, and body mass index was calculated as weight in kilograms divided by height in meters squared. Participants also reported their weight at age 25 years, which was used to calculate midlife weight gain (weight in 1974 − reported weight at age 25 years). Blood pressure and lipid levels were measured, and blood glucose level was measured 1 hour after a glucose load (1 g of oral glucose per kilogram of body weight). Alcohol consumption was assessed. One unit of alcohol (ie, a bottle of beer, a glass of wine, or 1 drink) was calculated to contain 14 g of alcohol. Participants also indicated quality of life in 1974 by rating their health and physical fitness on a 5-point scale (very good, good, fair, poor, or very poor).

Smoking status was assessed with a questionnaire. Participants were classified into 5 groups according to their reported smoking status in 1974: (1) never-smokers (n = 614), defined as men who had never smoked regularly and were not currently smoking; (2) ex-smokers (n = 650), defined as those who had been smokers before but had quit smoking by 1974; and participants who smoked (3) 1 to 10 cigarettes per day (n = 87), (4) 11-20 cigarettes per day (n = 119), or (5) more than 20 cigarettes per day (n = 188). The duration of the smoking habit or the time before 1974 when ex-smokers quit smoking was not available.

The 2000 survey

In 2000, a questionnaire was mailed to all 1286 survivors, and 1131 (87.9%) responded. The questionnaire included items on demographic variables and lifestyle (such as alcohol consumption, physical activity, weight, and the latest measured blood pressure value), including current smoking status. In addition, the Finnish version of the RAND 36-Item Health Survey 1.011 (similar to the Medical Outcomes Study Short-Form Survey [SF-36]) was embedded in the questionnaire. The RAND-36/SF-36 is perhaps the most widely used instrument to measure health-related quality of life (HRQoL).12 It has been shown to be a reliable, valid, and responsive instrument in measuring HRQoL of older people,13 and it has been validated as a mailed questionnaire in the Finnish general population.14 The RAND-36 comprises 36 items that assess 8 domains of HRQoL: physical functioning, role limitations caused by physical health problems, role limitations caused by emotional problems, social functioning, emotional well-being, energy/fatigue, pain, and general health perception. All scale scores range from 0 to 100, with 100 representing the most favorable functioning or well-being. A difference of at least 3 points is considered to be clinically significant.15 The physical functioning scale has been shown to be comparable to other instruments measuring disability in the elderly.16 The 8 domains of RAND-36 are further aggregated into 2 summary measures: the physical and mental health component summary scores. These summary scores are standardized so that the mean (−SD) for the validated population is 50 (−10).

Mortality follow-up

Total mortality of the study population through December 31, 2000, was retrieved from the National Population Information System of the Finnish Population Register Centre, which includes data from all Finnish citizens. Mortality information was available for all participants. The total follow-up time was as long as 26 years, generating 40 261 person-years of follow-up.

Statistical methods

We used NCSS statistical software for the analyses (NCSS, Kaysville, Utah). In statistical analyses, 2-tailed tests were used and P <.05 was considered significant. Analyses of covariance were used to compare continuous variables. Logarithmic transformations were used for variables with skewed distributions. Trend and χ2 tests were used to compare proportions, and Spearman rank coefficients were used to assess correlations. Differences in survival were analyzed using Kaplan-Meier curves and log-rank tests. Other risk factors were adjusted for in respective models.

Results
Baseline characteristics

Of 1658 men, 614 (37.0%) were never-smokers at baseline in 1974, and 650 (39.2%) had quit smoking earlier. There were 87 (5.3%), 119 (7.2%), and 188 (11.3%) participants who smoked 1 to 10, 11 to 20, and more than 20 cigarettes daily, respectively. The characteristics and cardiovascular risk factors for the different groups at baseline are presented in the Table. There were significant differences in several baseline variables among groups.

SMOKING, MORTALITY, AND HRQoL DURING FOLLOW-UP

In 2000, current smoking status was gathered from 1131 men. The median age of responders was 73 years (interquartile range, 70-76 years). The mean response rate was 87.9%. During follow-up, the cessation rate among smokers was substantial: 68.9% of those smoking more than 20 cigarettes to 82.1% of those smoking 1 to 10 cigarettes daily at baseline. Therefore, in 2000, only 78 respondents (6.9%) were currently smoking.

During the 26-year follow-up period, 372 of the 1658 men (22.4%) died. Figure 1 shows the association between smoking status in 1974 and mortality through 2000. The amount of daily cigarettes predicted mortality in a graded manner (P < .001).

The association between smoking status in 1974 and age-adjusted HRQoL in 2000 is illustrated as RAND-36 scale scores in Figure 2 and as RAND-36 physical and mental health component summary scores in Figure 3. The never-smokers had the highest (best) scores on all 8 RAND-36 scales, although the differences were not statistically significant for the scales expressing the mental and social aspects of quality of life. Especially large differences were seen for the scales of physical functioning and role limitations owing to physical health; never-smokers gained 13.7 and 11.7 higher points, denoting a difference of 17% and 16%, respectively, compared with those smoking more than 20 cigarettes a day (Figure 2). Compared with heavy smokers, never-smokers in our cohort lived 10 years longer (Figure 1). Meanwhile, the difference in their level of disability, as suggested by the 13.7-point difference in the physical functioning score, was equal to an age difference of 10 years when compared with the age- and sex-matched general Finnish population.14

The physical component summary score showed a graded deterioration of HRQoL with an increasing number of cigarettes smoked daily (global P = .01) (Figure 3). However, in multiple comparisons, only the difference between never-smokers and smokers of more than 20 cigarettes daily reached statistical significance.

The differences in RAND-36 scale scores remained similar among the smoking groups, adjusting for age and perceived health status in 1974. Differences in physical functioning (P < .001) and bodily pain (P = .04) scores remained statistically significant. The difference in physical component summary scores did not quite reach statistical significance (P = .09).

In a more extensive model adjusted for age and several variables in 1974 (perceived health, body mass index, 1-hour–postload glucose level, and alcohol consumption), the 8.5-point difference in the RAND-36 scale of physical functioning between never-smokers and those smoking more than 20 cigarettes daily remained statistically significant (P = .01).

Ex-smokers did not generally seem to reach the RAND-36 points of never-smokers during the 26-year follow-up.

CROSS-SECTIONAL ANALYSIS OF HRQoL AND SMOKING STATUS IN 2000

To compare our longitudinal findings with a cross-sectional setting in this cohort, we also carried out an analysis of RAND-36 among survivors according to their smoking status (smoking/not smoking) in 2000. In this analysis, the nonsmoking group also includes ex-smokers. It must be noted that between 1974 and 2000 many smokers had died and the ex-smokers in 2000 may have quit smoking owing to illness. Only 78 of 1131 men (6.9%) were still smokers in 2000, but they represent a cohort of truly long-term smokers. Hence, the cross-sectional viewpoint is quite different from the original longitudinal perspective.

The smokers in 2000 reported poorer scores on all 8 RAND-36 scales, and scores on 5 scales (physical functioning, energy/vitality, social functioning, role limitations owing to mental health problems, and mental health/emotional well-being) were significantly worse when adjusted for age and perceived health in 1974. Role limitations owing to physical health did not quite reach statistical significance (P = .07). Also, the 2.7-point difference in the mental health component summary score was significantly better for nonsmokers (P = .03), whereas the 1.8-point difference in physical component summary score was not statistically significant (P = .10). Therefore, although the differences in the physical domains of quality of life were more substantial in the longitudinal results according to smoking status in 1974, the worsening of the mental and social domains of HRQoL in smokers became statistically significant in this cross-sectional analysis.

Comment

Our study prospectively followed up a cohort of initially healthy men of similar socioeconomic status for whom smoking and risk factor data in midlife and quality of life and mortality data from 26 years later were available. Although many smokers had quit smoking between the baseline investigation in 1974 and the follow-up examination in 2000, the effect of baseline smoking status on mortality and the quality of life in old age remained strong. Cigarette smoking had a dose-dependent effect on mortality and RAND-36 scale scores, with heavy smokers having the worst results for both end points. In all, the results presented here are troubling for those who were smoking more than 20 cigarettes daily 26 years earlier; in spite of the 68.9% cessation rate during follow-up, 44.1% of the originally heavy smokers had died, and those who survived to the mean age of 73 years had a significantly lower physical HRQoL than never-smokers.

SMOKING AND HRQoL

In the present cohort, as well as in previous studies,17,18 a low cardiovascular risk factor profile in middle-age indicates better HRQoL later in life. But how lifetime smoking by itself affects HRQoL has not been clearly demonstrated. The effect of smoking on HRQoL has been investigated in cross-sectional studies of the general population,19-22 and shorter follow-up studies have been conducted for multiple diseases, showing the benefits of nonsmoking in these subgroups.23-25 However, few prospective studies have examined the effect of long-term smoking on HRQoL in old age.26,27 Likewise, few follow-up studies have investigated the HRQoL of ex-smokers.28,29 The evaluation of the association between smoking and HRQoL is complex because smoking is linked to many confounding factors, such as sex, sedentary lifestyle, educational level, and social class.30 Furthermore, the reasons for cessation range from psychosocial factors to ill health. Therefore, confounding may be difficult to control for in studies of the general population.

In our cohort, the exceptionally long follow-up time provides a unique opportunity to observe the effect of smoking in midlife on HRQoL in old age. The results are based on a large cohort of men with similar socioeconomic and job status. At baseline, participants were all healthy and had no chronic diseases and took no medications. The availability of data on several risk factors at baseline allowed us to perform multivariate adjustment for potential confounding factors, including alcohol consumption. Mortality follow-up with national registers was reliable. The HRQoL was measured with a widely used and validated instrument (RAND-36/SF-36), and there was an overall response rate of 88%. In addition, a particular strength of our study is that, although there were several conservative biases that could dilute the results, our data remained statistically significant. Consequently, our findings may better reflect the loss of HRQoL owing to smoking itself instead of preexisting disease.

The following factors possibly diluting the differences deserve consideration. First, because our cohort was healthy at baseline, we may have excluded men with tobacco-related diseases, producing a “healthy participant” bias. We did not investigate at which age each smoker began smoking, but because most smokers begin during adolescence,31 we can speculate that, in our cohort, many had been smoking for as long as 30 years in 1974. This probably explains the differences in perceived health at baseline. Second, the high rate of cessation of smoking during follow-up is likely to have diluted some of the harmful effects of smoking in our cohort, because quitting smoking has been shown to be beneficial for HRQoL.28 Cessation of smoking after baseline owing to illness may, in turn, negatively affect HRQoL and produce relatively better scores for smokers than quitters in 2000. The longitudinal design in the present study helps to investigate this possible bias. In fact, the physical functioning of the 78 men who were still smoking in 2000 was, on average, better than that of participants who were heavy smokers in 1974.

Similarly, there is a “healthy user” bias to be expected in the analysis of the HRQoL of surviving smokers in 2000. This cross-sectional analysis compares current nonsmokers, many of whom may have quit smoking because of illness, disability, or worse quality of life, with surviving smokers who were healthy enough to continue decades of smoking. Yet, the HRQoL of those 78 men still smoking in 2000, most of whom were likely lifetime smokers, was significantly worse compared with current nonsmokers. And the worse status of smokers was extended to the mental and social components of the RAND-36 as well.

Finally, because only survivors were assessed, and participants with poorer health are less likely to provide information, important data may be lost in late-life studies such as this one, which favors the group with the most deaths and missing data.32 Our 2000 questionnaire was conducted when mortality among the cohort was already considerable and significantly different among groups. It is therefore possible that there were more nonrespondents owing to ill health in the smokers' groups, again tending to weaken the negative effect of smoking on HRQoL in our study.

Limitations

The high cessation rate during follow-up may be regarded as a limitation, but it reflects the real-life change in the smoking habits of educated men from 1974 to 2000 in Finland33 and elsewhere.30 Another limitation is that we did not have any update of the changes in participants' smoking habits between 1974 and 2000. However, the aim of the present study was to investigate the baseline smoking status in relation to the end points in 2000. Furthermore, there were only 3 men who took up smoking between 1974 and 2000.

Another limitation is that we could not measure the baseline HRQoL with RAND-36/SF-36 in 1974 because this instrument was not used at that time. Assessed with the 5-point health measure, smokers already reported their perceived health status to be inferior to never-smokers at baseline. There are data demonstrating that the HRQoL of healthy young smokers already differs from nonsmokers in the first years of smoking.34 This indicates that those who are apt to take up smoking may have intrinsic psychological features, which are mirrored in their quality of life before the specific effects of smoking are evident. This may also partly explain the baseline differences between the groups in our study. However, the differences in HRQoL between the smoking groups in 2000 remained essentially similar when adjusted for age and subjective health in 1974.

Low socioeconomic status is associated with lower HRQoL.35 Although the socioeconomic similarity of our cohort has important advantages when evaluating the mechanistic association between smoking, mortality, and quality of life, extrapolation of the results to the general population and to women must be done cautiously.

Clinical and public health implications

Compared with heavy smokers, never-smokers had a mean life expectancy that was 10 years longer. They also enjoyed significantly better physical health status (assessed by the physical functioning scale of RAND-36) in late life, which was equal to an age difference of 10 years in the general population. This postponement of physical disability among never-smokers could implicate a similar lifetime burden of care among smokers and never-smokers, despite the longer lifespan of the latter. However, whether there is true compression of morbidity36,37 in the never-smokers' group, ie, a net reduction of disability, can only be assessed later as the cohort ages.

From a prevention point of view, our findings of the smoking/HRQoL relationship add to the view of the burden of smoking on society, and might at an individual level encourage smoking cessation. The argument of better quality of life may be especially meaningful for the aging smoker but, as our results show, for the best HRQoL, the habit should not be started at all. The highly addictive nature of nicotine is revealed by the persistence of the smoking habit in spite of the declining HRQoL among older heavy smokers. For those not able to quit smoking, reduction may also be beneficial because mortality and HRQoL showed a dose-dependent trend according to the number of cigarettes smoked daily.

Conclusion

Our longitudinal study shows that smoking status in middle age predicted HRQoL in old age, 26 years later, as well as mortality in a cohort of men who were healthy and socioeconomically homogeneous at baseline. Compared with never-smokers, heavy smokers lost about 10 years of their life-expectancy, and those who survived experienced a significant decline in their quality of life.

Correspondence: Arto Y. Strandberg, MD, Department of Medicine, Geriatric Clinic, University of Helsinki, PL 340, 00029 Helsinki, Finland (arto.strandberg@kolumbus.fi).

Accepted for Publication: February 18, 2008.

Author Contributions: Drs Strandberg, Salomaa, and Miettinen had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: A. Y. Strandberg and T. E. Strandberg. Acquisition of data: A. Y. Strandberg, T. E. Strandberg, and Miettinen. Analysis and interpretation of data: A. Y. Strandberg, T. E. Strandberg, Pitkälä, Salomaa, Tilvis, and Miettinen. Drafting of the manuscript: A. Y. Strandberg and T. E. Strandberg. Critical revision of the manuscript for important intellectual content: Pitkälä, Salomaa, Tilvis, and Miettinen. Statistical analysis: Salomaa. Obtained funding: T. E. Strandberg. Administrative, technical, and material support: T. E. Strandberg, A. Y. Strandberg, Pitkälä, and Tilvis. Study supervision: A. Y. Strandberg, T. E. Strandberg, and Miettinen.

Financial Disclosure: None reported.

Funding/Support: This study was supported by The Academy of Finland, the Sohlberg Foundation, the Ida Montin Foundation, Helsinki University Central Hospital, and the Finnish Foundation for Cardiovascular Research.

Role of the Sponsor: The sponsors had no role in the design or conduct of the study; collection, management, analysis, and interpretation of the data; or preparation, review, or approval of the manuscript.

Additional Contributions: We thank the participants in the Helsinki Businessmen Study for their dedication.

References
1.
Doll  RPeto  RBoreham  JSutherland  I Mortality in relation to smoking: 50 years' observations on male British doctors.  BMJ 2004;328 (7455) 1519- 1533PubMedGoogle Scholar
2.
Brønnum-Hansen  HJuel  K Abstention from smoking extends life and compresses morbidity: a population-based study of health expectancy among smokers and never smokers in Denmark.  Tob Control 2001;10 (3) 273- 278PubMedGoogle Scholar
3.
Martel  LBelanger  ABerthelot  J Smoking and disability-free life expectancy in Canada. Bélanger  ACarrière  YGilbert  S Report on the Demographic Situation in Canada. Ottawa, Quebec, Canada Statistics Canada, Demography Division2000;111- 134Google Scholar
4.
Rogers  RGPowell-Griner  E Life expectancies of cigarette smokers and nonsmokers in the United States.  Soc Sci Med 1991;32 (10) 1151- 1159PubMedGoogle Scholar
5.
Dallongeville  JMarecaux  NFruchart  JC  et al.  Cigarette smoking is associated with unhealthy patterns of nutrient intake: a meta-analysis.  J Nutr 1998;128 (9) 1450- 1457PubMedGoogle Scholar
6.
Jarvis  MWardle  J Social patterning of individual health behaviours: the case of cigarette smoking. Marmot  MWilkinson  R Social Determinants of Health. Oxford, England Oxford University Press1999;240- 255Google Scholar
7.
Mamun  AAPeeters  ABarendregt  JWillekens  FNusselder  WBonneux  L Smoking decreases the duration of life lived with and without cardiovascular disease: a life course analysis of the Framingham Heart Study.  Eur Heart J 2004;25 (5) 409- 415PubMedGoogle Scholar
8.
Guralnik  JMKaplan  GA Predictors of healthy aging: prospective evidence from the Alameda County study.  Am J Public Health 1989;79 (6) 703- 708PubMedGoogle Scholar
9.
Ebrahim  SWannamethee  SGWhincup  PWalker  MShaper  AG Locomotor disability in a cohort of British men: the impact of lifestyle and disease.  Int J Epidemiol 2000;29 (3) 478- 486PubMedGoogle Scholar
10.
Miettinen  TAHuttunen  JKNaukkarinen  V  et al.  Multifactorial primary prevention of cardiovascular diseases in middle-aged men: risk factor changes, incidence, and mortality.  JAMA 1985;254 (15) 2097- 2102PubMedGoogle Scholar
11.
Hays  RDMorales  LS The RAND-36 measure of health-related quality of life.  Ann Med 2001;33 (5) 350- 357PubMedGoogle Scholar
12.
Garratt  ASchmidt  LMackintosh  AFitzpatrick  R Quality of life measurement: bibliographic study of patient assessed health outcome measures.  BMJ 2002;324 (7351) 1417- 1422PubMedGoogle Scholar
13.
Haywood  KLGarratt  AMFitzpatrick  R Quality of life in older people: a structured review of generic self-assessed health instruments.  Qual Life Res 2005;14 (7) 1651- 1668PubMedGoogle Scholar
14.
Aalto  A-MAro  ARTeperi  J RAND-36 as a Measure of Health-Related Quality of Life: Reliability, Construct Validity, and Reference Values in the Finnish General Population.  Helsinki, Finland STAKES1999;STAKES Research Report 101
15.
Ware  JEKosinski  M SF-36 Physical and Mental Health Summary Scales: A Manual for Users of Version 1. 2nd ed. Lincoln, RI QualityMetric Inc2001;
16.
Dubuc  NHaley  SMNi  PKooyoomjian  JTJette  AM Function and disability in late life: comparison of the Late-Life Function and Disability Instrument to the Short-Form-36 and the London Handicap Scale.  Disabil Rehabil 2004;26 (6) 362- 370Google Scholar
17.
Daviglus  MLLiu  KPirzada  A  et al.  Favorable cardiovascular risk profile in middle age and health-related quality of life in older age.  Arch Intern Med 2003;163 (20) 2460- 2468PubMedGoogle Scholar
18.
Strandberg  AStrandberg  TESalomaa  VVPitkälä  KHappola  OMiettinen  TA A follow-up study found that cardiovascular risk in middle age predicted mortality and quality of life in old age.  J Clin Epidemiol 2004;57 (4) 415- 421PubMedGoogle Scholar
19.
Tillmann  MSilcock  J A comparison of smokers' and ex-smokers' health-related quality of life.  J Public Health Med 1997;19 (3) 268- 273PubMedGoogle Scholar
20.
Lyons  RALo  SVLittlepage  BNC Perception of health amongst ever-smokers and never-smokers: a comparison using the SF-36 Health Survey Questionnaire.  Tob Control 1994;3213- 21510.1136/tc.3.3.213Google Scholar
21.
Mody  RRSmith  MJ Smoking status and health-related quality of life: as findings from the 2001 Behavioral Risk Factor Surveillance System data.  Am J Health Promot 2006;20 (4) 251- 258PubMedGoogle Scholar
22.
Wilson  DParsons  JWakefield  M The health-related quality-of-life of never smokers, ex-smokers, and light, moderate, and heavy smokers.  Prev Med 1999;29 (3) 139- 144PubMedGoogle Scholar
23.
Taira  DASeto  TBHo  KK  et al.  Impact of smoking on health-related quality of life after percutaneous coronary revascularization.  Circulation 2000;102 (12) 1369- 1374PubMedGoogle Scholar
24.
Turner  JPage-Shafer  KChin  DP  et al.  Adverse impact of cigarette smoking on dimensions of health-related quality of life in persons with HIV infection.  AIDS Patient Care STDS 2001;15 (12) 615- 624PubMedGoogle Scholar
25.
Garces  YIYang  PParkinson  J  et al.  The relationship between cigarette smoking and quality of life after lung cancer diagnosis.  Chest 2004;126 (6) 1733- 1741PubMedGoogle Scholar
26.
Østbye  TTaylor  DH The effect of smoking on years of healthy life (YHL) lost among middle-aged and older Americans.  Health Serv Res 2004;39 (3) 531- 552PubMedGoogle Scholar
27.
Thorn  JBjorkelund  CBengtsson  CGuo  XLissner  LSundh  V Low socio-economic status, smoking, mental stress and obesity predict obstructive symptoms in women, but only smoking also predicts subsequent experience of poor health.  Int J Med Sci 2007;4 (1) 7- 12PubMedGoogle Scholar
28.
Croghan  ITSchroeder  DRHays  JT  et al.  Nicotine dependence treatment: perceived health status improvement with 1-year continuous smoking abstinence.  Eur J Public Health 2005;15 (3) 251- 255PubMedGoogle Scholar
29.
Mitra  MChung  MCWilber  NKlein Walker  D Smoking status and quality of life: a longitudinal study among adults with disabilities.  Am J Prev Med 2004;27 (3) 258- 260PubMedGoogle Scholar
30.
Goddard  E Smoking and Drinking Among Adults, 2005.  London, England Office for National Statistics2006;General Household Survey 2005
31.
 The 1991 National Household Survey on Drug Abuse.  Research Triangle Park, NC Research Triangle Institute1991; Preventing Tobacco Use Among Young People: A Report of the Surgeon General US. Atlanta, GA Dept of Health and Human Services1994;Google Scholar
32.
Diehr  PJohnson  LL Accounting for missing data in end-of-life research.  J Palliat Med 2005;8 ((suppl 1)) S50- S57PubMedGoogle Scholar
33.
 Tobacco Statistics 2005.  Helsinki, Finland Statistics Finland2006;Official Statistics of Finland, Health 2006 Report Series
34.
Martinez  JAMota  GAVianna  ESFilho  JTSilva  GARodrigues  AL  Jr Impaired quality of life of healthy young smokers.  Chest 2004;125 (2) 425- 428PubMedGoogle Scholar
35.
Chandola  TFerrie  JSacker  AMarmot  M Social inequalities in self reported health in early old age: follow-up of prospective cohort study.  BMJ 2007;334 (7601) 990- 997PubMedGoogle Scholar
36.
Fries  JFGreen  LWLevine  S Health promotion and the compression of morbidity.  Lancet 1989;1 (8636) 481- 483PubMedGoogle Scholar
37.
Nusselder  WJLooman  CWNMarang–van de Mheen  PJvan de Mheen  HMackenbach  JP Smoking and the compression of morbidity.  J Epidemiol Community Health 2000;54 (8) 566- 574PubMedGoogle Scholar
×