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Julia Hippisley-Cox a Division of General Practice,
School of Community Health Sciences, University of Nottingham,
Nottingham NG7 2RD, b Collingham Medical Centre, Collingham NG23 7LB Correspondence to:
J Hippisley-Cox julia.hippisley-cox{at}nottingham.ac.uk
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Abstract |
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Objective:
To determine whether people
whose marital partners have depression, diabetes, hypertension,
ischaemic heart disease, stroke, hyperlipidaemia, peptic ulcer disease, or asthma or chronic obstructive pulmonary disease are at increased risk of the same disease.
Design:
Cross sectional study.
Setting:
10 practices from the Trent Focus
Collaborative Research Practice Network.
Participants:
8386 married couples
(16 772 individuals) from a population of 29 014 participants aged
30-74 years.
Outcomes:
Risk of disease in participants whose
marital partner had that disease compared with those whose partner did not.
Results:
After both partners' age,
smoking, and obesity and which general practice they attend were
adjusted for, participants whose marital partner had asthma,
depression, hypertension, hyperlipidaemia, and peptic ulcer disease
were at increased risk of having the same disease. The adjusted odds
ratios were 1.69 (95% confidence interval 1.43 to 2.98) for asthma,
2.08 (1.71 to 2.54) for depression, 1.32 (1.04 to 1.67) for
hypertension, 1.44 (1.19 to 1.75) for hyperlipidaemia, and 2.01 (1.48 to 2.73) for peptic ulcer disease.
Conclusion:
Partners of people with specific diseases are at increased risk of the disease themselves
at least 70%
increased risk for asthma, depression, and peptic ulcer disease. This
implicates shared environmental causes in some diseases in addition to
any genetic or distant exposure or shared behaviours with respect to
seeking health care.
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What is already known on this topic
Little is known about the risks of disease for spouses of patients with diseases other than hypertension What this study adds
Shared environmental factors contribute to the risk of diseases The costs and benefits of screening people for diseases of their spouses needs to be considered |
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Introduction |
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Studies in twins have clarified the contributions of genetic and environmental factors to the development of diseases by identifying genetic factors. 1 2 The study of cohabiting couples can identify environmental factors. Shared environmental factors may put cohabiting partners at risk of the same diseases, and this could have implications for screening and other interventions. Interventions targeted at couples may be more effective than those targeted at individuals.3
In 1998, we published a study from a single practice that showed an
association between having a spouse with hypertension and increased
risk of hypertension.4 Apart from one large, population
based study that showed statistically significant husband-wife associations for cancers of the tongue and stomach and for
non-Hodgkin's lymphoma,5 we found no adequate evidence
for spouse concordance for many other common but important diseases,
such as ischaemic heart disease, diabetes, peptic ulcer disease,
asthma, and stroke. Some small studies showed concordance between
married couples for psychological wellbeing,6 dietary
habits,7 and warfarin dosage.8 Results from
studies of coronary risk factors have been inconsistent
some but not
all found concordance, particularly when age, body weight, and smoking
status were adjusted for.9-14
We aimed to determine whether people whose marital partners have a
specific disease are at increased risk of the same disease. We studied
common and important diseases in which plausible biological environmental mechanisms could have a role (asthma or chronic obstructive pulmonary disease, depression, diabetes, hypertension, ischaemic heart disease, stroke, hyperlipidaemia, or peptic ulcer disease).
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Methods |
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We conducted a cross sectional study in 10 general practices with data of proved quality from the Trent Focus Collaborative Research Network. The study population consisted of all registered patients aged 30-74 years inclusive.
We used computerised records to identify participants with and without each of the eight diseases (see bmj.com). Records with a Read code or current related treatment, or both, identified participants with the disease. We extracted the first recorded date of onset of each of the eight diseases for all patients in the study population. For related drugs, we extracted dates and number of prescriptions. We defined the current use of a drug as more than one prescription within the previous 12 months.
We defined a married couple as "two individuals aged 30-74 years living at the same address; of different sex; and with the same surname, titles of Mr and Mrs, and a difference in age of less than 15 years." This definition identified married couples living together, but it excluded cohabiting or same sex couples.
Statistical analysis
We used an unconditional logistic regression analysis to calculate
odds ratios and 95% confidence intervals for the risk of disease in
participants whose marital partner had a particular disease compared
with those whose marital partner did not. We used female disease status
as the outcome variable and male disease status as the exposure
variable. We adjusted for the possible confounding effects of age of
both partners and, in further analyses, for the possible confounding
effects of most recently recorded category for obesity and of most
recently recorded smoking status in both partners. We allowed for
clustering by general practice.
We used Pearson's correlation coefficient to determine the correlation
between couples for body mass index. We calculated a partial
correlation coefficient that adjusted for both partners' ages. We
coded the most recent blood pressure reading into high (systolic
160
mm Hg or diastolic
90 mm Hg) or not high (this category included
missing values), and we calculated odds ratios adjusted for the
participants' and partners' ages, obesity, smoking status, and
general practice. We calculated age adjusted odds ratios to quantify
spouses' concordance for smoking. We used a two tailed significance
level of 0.01 for the main outcome variables because of the number of
outcomes under investigation.
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Results |
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Characteristics of the study population
In total, 29 014 people aged 30-74 living in households with only
one or two adults in this age range were registered with the 10 practices. Of these, 8386 women (56.8% of 14 757 women aged 30-74)
and 8386 men (58.8% of 14 257 men aged 30-74) were part of a married
couple according to our definition. The baseline characteristics are
presented on bmj.com.
Risk of disease in participants whose marital partner has disease
Participants whose marital partner had asthma, depression,
hypertension, hyperlipidaemia, or peptic ulcer disease were at
increased risk of having the disease themselves after we adjusted for
age, obesity, and smoking status in both partners and for the general
practice at which the participants were registered (table). The odds
ratio for diabetes was higher in women whose partners had diabetes than
in those whose partners did not, but the confidence intervals were wide
because of the low prevalence of diabetes compared with most of the
other diseases we studied. The odds ratios for ischaemic heart disease
and stroke were higher in women whose spouses had these diseases, but
this was not statistically significant (table).
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On multivariate analysis, the adjusted odds ratio for high blood
pressure in women whose partners had high blood pressure compared with
those whose partners did not was 1.40 (95% confidence interval 1.19 to
1.64). The correlation between marital partners for body mass index was
significant (r=0.21, P<0.001). When we adjusted for the
age of both partners, the partial correlation was 0.20 (P<0.001). We
found a significant association between married partners for smoking
status (P<0.001)
the age adjusted odds ratio for participants being
smokers was 4.4 (3.8 to 5.1) for those whose partners were current
smokers or former smokers compared with non-smokers. We repeated the
analyses including only married couples for whom complete data on
smoking and body mass index were available (2654 couples, 31.6%) and
found no important differences in the odds ratios.
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Discussion |
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Participants were significantly more likely to have asthma,
depression, hypertension, hyperlipidaemia, or peptic ulcer disease if
their marital partner had the same disease. The increased risks
at least 70% for asthma, depression, and peptic ulcer disease
could indicate shared environmental causes for diseases, which are distinct from any genetic or distant exposures. Another explanation for our
findings is that couples may share healthcare seeking behaviours, although this would not explain the concordance for high blood pressure. The findings could have implications for targeting screening or disease prevention measures at partners of participants with one of
these diseases.
Although the results were not surprising for some of these diseases, the findings for hypertension and hyperlipidaemia suggest that diet or the pattern of physical exercise shared by couples has an important role in the disease's cause. A consequent association for ischaemic heart disease and stroke might have been expected, but this was not found. The finding for asthma might be due to shared diet or shared exposure to allergens. The failure of diabetes to show a significant concordance for marital partners (although the adjusted odds ratio was 1.41) was unexpected, but it was probably because the prevalence of diabetes was lower than that for most of the other diseases we studied and our study was not sufficiently powered to taken into account this low prevalence.
Strength and weaknesses of the study
A limitation of our study is that we did not obtain consultation
data; this means that we could not adjust for the different frequencies
at which some groups of patients consult their general practitioner.
This could affect patients' chances of being screened for a disease,
being diagnosed with a disease, or having a diagnosis recorded on
computer. Spouses of affected participants may be more aware of the
early symptoms of a particular disease, and this may make them more
likely to consult their general practitioner and be screened.
The study's strengths are its large sample size, the quality of data from the general practices, the selection of community participants, and the use of multivariate analysis to adjust for potential confounders. Our method of data collection means that the study is unlikely to be susceptible to selection and recall bias.
The data could be at risk of misclassification bias because disease status may have been falsely classified as negative or falsely classified as positive. Misclassification would have reduced the odds ratio of the factor under investigation.15 Bias due to missing data is unlikely to have affected our results substantially because our findings were similar when we analysed only patients with complete data. We also reduced the effect of selection bias by including categories for patients with missing data about smoking and obesity.15
Previous studies suggested that concordance for some conditions (for example, hypertension) could be due to positive "assortive mating."9 For example, if obese people are more likely to have obese marital partners, they could share an increased risk of disease due to their obesity or factors related to its development (such as lack of physical activity). If positive assortive mating was present, the association between exposure to a marital partner with a disease and the risk of that disease would have been reduced by the inclusion of body mass index in the multivariate analysis. This was not the case.
Another limitation is that we have no information on the length of time that participants had been couples or on the sequence of events. Our study design allowed us to show associations rather than causality.
Conclusion
The high increased risks of disease within married couples support
the idea that shared environmental factors in addition to genetic or
distant exposures contribute to the development of diseases. Screening
spouses for some diseases should be considered.
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Acknowledgments |
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We thank the practices of the Trent Focus Collaborative Research Network for participating in this study.
Contributors: See bmj.com
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Footnotes |
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Funding: Culyer research and development funding, NHS Executive Trent.
Competing interests: None declared.
The full version of this article
appears on bmj.com
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References |
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|
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| 1. |
Spector T, Cicuttini F, Baker J, Loughlin J, Hart D.
Genetic influences on osteoarthritis in women: a twin study.
BMJ
1996;
312:
940-944 |
| 2. |
Rose R, Miller J, Grim CE, Christian JC.
Aggregation of blood pressure in the families of identical twins.
Am J Epidem
1979;
109:
503-511 |
| 3. | Sexton M, Bross D, Hebel R, Schumann BC, Gerace TA, Lasser N, et al. Risk-factor changes in wives with husbands at high risk of coronary heart disease: the spin off effect. J Behav Med 1987; 10: 3. |
| 4. | Hippisley-Cox J, Pringle M. Are spouses of patients with hypertension at increased risk of hypertension? A population based case-control study. Br J Gen Pract 1998; 46: 1580-1584. |
| 5. | Friedman GD, Quesenberry Jr CP. Spousal concordance for cancer incidence: a cohort study. Cancer 1999; 86: 2413-2419[CrossRef][Web of Science][Medline]. |
| 6. | Galbaud Du Fort G, Kovess V, Boivin JF. Spouse similarity for psychological distress and well-being: a population study. Psychol Med 1994; 24: 431-447[Web of Science][Medline]. |
| 7. |
Davis M, Murphy S, Neuhaus J, Gee L, Quiroga S.
Living arrangements affect dietary quality for US adults aged 50 years and older: NHANES III 1998-1994.
J Nutrition
2000;
130:
2256-2264 |
| 8. |
Van Haeften T, de Vries J, Sixma J.
Concordance of phenprocoumon dosage in married couples.
BMJ
1997;
314:
1386 |
| 9. |
Sackett DL, Anderson GD, Milner R, Feinleib M, Kannel WB.
Concordance for coronary risk factors among spouses.
Circulation
1975;
52:
589-595 |
| 10. | An P, Rice T, Gagnon J, Borecki IB, Perusse L, Leon AS, et al. Familial aggregation of resting blood pressure and heart rate in a sedentary population: the heritage family study. Health, risk factors, exercise training, and genetics. Am J Hypertens 1999; 12: 264-270[CrossRef][Web of Science][Medline]. |
| 11. | Brenn T. Adult family members and their resemblance of coronary heart disease risk factors: the cardiovascular disease study in Finnmark. Eur J Epidemiol 1997; 13: 623-630[CrossRef][Web of Science][Medline]. |
| 12. | Kolonel LN, Lee J. Husband-wife correspondence in smoking, drinking, and dietary habits. Am J Clin Nutr 1981; 1: 99-104. |
| 13. |
Rissanen AM, Nikkila EA.
Aggregation of coronary risk factors in families of men with fatal and non-fatal coronary heart disease.
Br Heart J
1979;
42:
373-380 |
| 14. |
Garrison RJ, Castelli WP, Feinleib M, Kannel WB, Havlik RJ, Padgett SJ, et al.
The association of total cholesterol, triglycerides and plasma lipoprotein cholesterol levels in first degree relatives and spouse pairs.
Am J Epidemiol
1979;
110:
313-321 |
| 15. | Breslow NE, Day NE. Statistical methods in cancer research. Lyon: IARC Scientific Publications, 1987. |
(Accepted 1 May 2002)
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