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Medical Science Monitor: International Medical Journal of Experimental and Clinical Research logoLink to Medical Science Monitor: International Medical Journal of Experimental and Clinical Research
. 2014 May 23;20:843–852. doi: 10.12659/MSM.890100

Edentulism and other variables associated with self-reported health status in Mexican adults

Carlo Eduardo Medina-Solís 1,2,A,C,D,E,F,, América Patricia Pontigo-Loyola 1,A,D,E, Eduardo Pérez-Campos 2,3,A,D,E, Pedro Hernández-Cruz 2,3,A,D,E, Leticia Avila-Burgos 4,A,D,E, Martha Mendoza-Rodríguez 1,A,D,E, Gerardo Maupomé 5,6,A,C,D,E
PMCID: PMC4043565  PMID: 24852266

Abstract

Background

To determine if edentulism, controlling for other known factors, is associated with subjective self-report health status (SRH) in Mexican adults.

Material/Methods

We examined the SRH of 13 966 individuals 35 years and older, using data from the National Survey of Performance Assessment, a cross-sectional study that is part of the technical collaboration between the Ministry of Health of Mexico and the World Health Organization, which used the survey instrument and sampling strategies developed by WHO for the World Health Survey. Sociodemographic, socioeconomic, medical, and behavioral variables were collected using questionnaires. Self-reported health was our dependent variable. Data on edentulism were available from 20 of the 32 Mexican states. A polynomial logistic regression model adjusted for complex sampling was generated.

Results

In the SRH, 58.2% reported their health status as very good/good, 33.8% said they had a moderate health status, and 8.0% reported that their health was bad/very bad. The association between edentulism and SRH was modified by age and was significant only for bad/very bad SRH. Higher odds of reporting moderate health or poor/very poor health were found in women, people with lower socio-economic status and with physical disabilities, those who were not physically active, or those who were underweight or obese, those who had any chronic disease, and those who used alcohol.

Conclusions

The association of edentulism with a self-report of a poor health status (poor/very poor) was higher in young people than in adults. The results suggest socioeconomic inequalities in SRH. Inequality was further confirmed among people who had a general health condition or a disability.

Keywords: Self-Reported Health, Oral Health, Edentulism, Socioeconomic Inequalities

Background

In general, there are 2 ways to measure the health status of a population. One is a subjective approach by asking the individual, and then using the self-reported health status to summarize symptoms, disease, injuries, or disability. The other is by using normative method using skilled health personnel and a clinical exam [1]. In the first case, the individual notices changes in his/her normal state of wellness. These perceptions (deviations from the “normal” state) are subjective, and are based on the accumulation of past experiences, both by the individual and by those around him/her. In the second case, the criteria are based on a normative assessment by health personnel that meets clinical standards of what constitutes a structural and/or functional deviation for the tissue, organ, system, or the body as a whole [2]. For several years there has been growing interest in measures of self-perceived health status in clinical scenarios, in therapy programs, and in health surveys. Self-reported health is one of the most frequently used measures of health perceptions evaluated in social epidemiology [3,4]. It is a common synthesis of health conditions that, despite lacking direct clinical equivalence, correlates with more complex health measures. It incorporates a bio-psychosocial construct not captured by other morbidity measures [5]. By its very nature, self-rated (self-perceived) health has a subjective component that reflects objective health evaluations of the past as well as future expectations. It is a relatively stable measure over time, and shows high test–re-test reliability [4,6]. It has also been demonstrated that self-rated health is a powerful predictor of both morbidity [6,7,8] and mortality [9,10].

In Latin America and Mexico there have been few studies concerning self-reported health [1115]. Several variables have been associated with self-reported poor health. Studies around the world have found changes associated with variables such as age [6,1518], sex [6,1821], physical activity [15,22], various indicators of socioeconomic position [4,12,15,1719,21,22] chronic diseases, body-mass index (BMI) and other health conditions [6,12,15,18,21,23], physical activity [12,15,18,22,24], having a healthy diet [18], religiosity [18], sleep quality [18], and consumption of alcohol and tobacco [15,25,26], among others.

Although studying variables associated with self-reported general health is not new, the association with oral conditions has not been fully studied. The information applicable to Mexico is non-existent in this area. The objective of the present study was to determine if edentulism, socioeconomic position, socio-demographic variables, and presence of other health problems or disabilities were associated with self-reported general health in a Mexican adult population.

Material and Methods

Study design and population

The present study was derived from secondary analyses of health survey data from a nationally representative sample in Mexico. Further details of the survey are available elsewhere [2730]. Briefly, the National Performance Evaluation Survey 2002–2003 (ENED), a cross-sectional study, was part of the technical collaboration between the Ministry of Health of Mexico (SSA) and the World Health Organization, which used the survey instrument and sampling strategies developed by WHO for the World Health Survey (WHS) [31]. Information was collected from 38 746 households, with a mean of 1250 households for each State. The sample design was probabilistic, multistage, stratified, through conglomerates, and was calculated to provide representative information at the State level, and across urban and rural areas. The sample size considered 9% as the smaller proportion to estimate; State estimations with a maximum relative error of 25%; a confidence level of 95%; non-response rate of 15%; and a design effect of 1.7. The complete WHS instrument was not used in every State. Data on dental conditions were only available for 20 out of the 32 States of Mexico, leading to a total of 24 159 households included in the present study. Three strata were considered: a) cities or metropolitan areas (locations with more than 100 000 inhabitants); b) urban settings (locations from 2500 to 99 999 inhabitants), and c) rural areas (locations with fewer than 2500 inhabitants). The final sample comprised 13 966 participants.

Data collection

The ENED survey had 2 different questionnaires, with 1 questionnaire inquiring about household conditions and the other inquiring about individual subject factors. In the first questionnaire, information was gathered on neighborhood public services, income, expenses, and health insurance. The second questionnaire gathered information including health status, health risk factors, presence of key diseases, use of health services, non-clinical expectations of the population, and insurance coverage of certain clinical services. The interview time was approximately 110 minutes per household.

Variables and instruments

Dependent variable

Self-reported health was our dependent variable, and was assessed by an item consisting of 5 alternatives. The first option entailed completely good health (“very good”). The second option was a straightforward “good”. The third option was neutral, coded as “moderate”. The fourth and fifth options were “bad” and “very bad”. In this study, self-reported health was categorized into good (the two first alternatives), moderate, and bad (the 2 remaining options).

Independent variables

The main independent variable was edentulism, which refers to the absence of any natural teeth in the mouth; it was gathered through question Q6757,Have you lost all of your natural teeth?” In addition, a series of socio-demographic, socio-economic factors, and variables related to health were included: age (35 to 98 years), sex (male or female), residence (rural, urban, metropolitan), marital status (single, married, divorced, widowed, cohabitating), indigenous ethnicity status (”Do you speak an indigenous language?”: no or yes), schooling (less than elementary, complete elementary, complete secondary, high school/equivalent, college studies/higher), occupation (employed in the public sector, employed outside the public sector, self-employed, or not working or doing volunteer work), health insurance (insured or non-insured), socio-economic level (in tertiles), having a disability (none or yes), physical activity (high activity or low activity), chronic disease (none or any), body mass index (BMI; underweight <18.5, normal 18.5–24.9, overweight 25.0–29.9, or obesity ≥30), and tobacco use (never/not currently, sometimes, or daily) and alcohol use (Never and low: fewer than 4 servings for women and 5 for men in the last week on 1 occasion; or high: 4 servings and more for women, and 5 for men in the last week on 1 occasion) [32]. Valid data were BMI values between 10 and 58; for height, we considered valid data between 130 and 200 cm [33]. We excluded from analysis data outside acceptable limits for BMI (n=24) and for height (n=48).

Disability

This variable was constructed through interviewer’s reporting problems with walking, being confined to a wheelchair, or using cane, crutches, or walker. Those reporting at least 1 limb paralyzed or amputated, and those with medically diagnosed mental health problems, were also included in this category.

Socio-economic level

The household survey included general topics, such as building materials of the house and ownership of consumable goods, which led to a Wealth Index using principal components analysis (PCA). Owning a refrigerator, washing machine, dishwasher, personal computer, car, bicycle, television, etc., were the goods combined in the polycoric PCA [34]. The aspects incorporated to assess features of the home included the building materials for walls and floor, the number of rooms, the characteristics of bathroom and kitchen, the source of potable or indoor water, having electricity and heating, and an estimate of whether the household could be considered overcrowded.

There were some missing data for weight (n=243), height (n=367), indigenous ethnicity status (n=113), insurance (n=30), and socio-economic level (n=1), which were imputed through regression imputation [35].

Statistical analysis

First, a univariate analysis was conducted to report the summary measures per case (for nominal and ordinal variables, frequencies and percentages; for continuous variables, dispersion and central tendency measures). Assuming an ordinal behavior of the dependent variable, a model of ordered logistic regression was used. It was later changed for the multinomial (polytomous) logistic regression model, since the assumption of similar coefficients among categories was not met (proportional odds assumption) in some independent variables in the bivariate analyses [34]. In the multinomial logistic regression, results are established based on a comparison category. In our case, we selected as the comparison category for the dependent variable the “very good/good” category of self-reported health. The role of each of the variables was thus identified while controlling for the remaining variables, and for their interactions, thus offering an overview of the associations between variables and the performance of the model as a whole [36]. We first ran the model using bivariate techniques, reporting odds ratio (OR), 95% confidence intervals (CI 95%), and p-value of the test. Finally, a multivariate multinomial logistic regression model was constructed and incorporated all variables available that at the bivariate analysis level exhibited a p-value <0.25, to control for possible confusion.37 The criterion for inclusion of variables in the multivariate model was its association with health perception at a level of p <0.05, but we considered a p<0.10 as a trend to be associated with the response variable. We used the module svy (complex samples) of the statistical package STATA 9®.

Ethical consideration

The Medical Research Committee of the National Institute of Public Health in Mexico granted ethics approval. Participation in the survey was voluntary. All individuals provided written informed consent.

Results

In this analysis, we included only individuals 35 years old and older (n=13,966), representing 29 853 607 inhabitants of 20 States of Mexico. Tables 1 and 2 show the descriptive data of the study. The majority of participants (40.4%) were 35–44 years old and 57.9% were women. The highest percentage (49.5%) lived in a metropolitan zone, 67.2% were married, and 8.1% were considered of indigenous ethnicity. In relation to the socioeconomic position indicator variables, we observed that 48.9% of the subjects had completed elementary school; most of them did not work or worked on a voluntary basis without remuneration (52.7%) and of these the majority were women (82.8%); 61.1% did not have health insurance. In the health-related variables, we observed that 10.2% (representing 3 052 263 individuals) were edentulous; a similar percentage had physical disabilities; 92.2% reported performing moderate to vigorous physical activity; 16.6% had a diagnosed chronic disease; a considerable proportion of the population were overweight/obese (42.1% and 19.7%, respectively); 77.3% had never smoked; and 59.7% said that they did not drink alcohol.

Table 1.

Socio-demographic and socio-economic characteristics of the study population across categories of self-reported general health (estimated population N=29,853,607).

Variable n N (% weighted) VG/G Moderate B/VB p value
Age 0.0000
 35–44 years 5,095 12,053,147 (40.4) 67.9 27.6 4.5
 45–59 years 4,658 10,224,403 (34.2) 55.9 36.0 8.1
 60 and more years 4,213 7,576,057 (25.4) 45.9 40.8 13.4

Sex 0.0000
 Male 5,975 12,557,585 (42.1) 63.2 30.5 6.3
 Female 7,991 17,296,022 (57.9) 54.5 36.3 9.2

Residence 0.2730
 Rural 4,132 7,956,031 (26.7) 57.0 34.3 8.7
 Urban 3,970 7,110,123 (23.8) 56.9 35.5 7.6
 Metropolitan 5,864 14,787,453 (49.5) 59.4 32.8 7.8

Marital status 0.0000
 Single 997 1,802,953 (6.0) 63.2 29.3 7.5
 Married 8,867 20,073,180 (67.2) 60.1 32.8 7.1
 Divorced 1,011 1,854,057 (6.2) 56.3 35.2 8.4
 Widowed 2,023 3,358,374 (11.2) 43.7 43.4 12.9
 Cohabitating 1,068 2,765,043 (9.3) 60.0 31.6 8.4

Indian ethnicity status 0.0050
 No 13,154 27,439,358 (91.9) 57.6 34.4 8.0
 Yes 812 2,414,249 (8.1) 65.5 26.9 7.6

Schooling 0.0000
 Less than elementary 3,151 6,308,017 (21.1) 52.1 36.0 11.9
 Complete elementary 6,834 14,594,709 (48.9) 55.1 36.7 8.2
 Complete middle school 1,911 4,401,463 (14.7) 64.3 30.3 5.4
 High School/equivalent 1,176 2,698,823 (9.0) 69.5 25.4 5.1
 College and higher 894 1,850,595 (6.2) 72.2 24.3 3.4

Occupation 0.0000
 Government Employee 1,243 2,300,766 (7.7) 70.0 27.5 2.5
 Non-Government Employee 1,349 3,070,293 (10.3) 71.5 23.6 4.9
 Self-Employed 4033 8,672,457 (29.0) 61.2 32.7 6.0
 Employer 46 61,221 (0.2) 61.9 26.2 11.8
 Volunteer Worker 51 111,870 (0.4) 62.8 35.4 1.8
 Does not work 7244 15,637,000 (52.7) 52.1 37.4 10.5

Health insurance 0.7948
 Non-insured 8,442 18,251,697 (61.1) 58.4 33.5 8.1
 Insured 5,524 11,601,910 (38.9) 57.8 34.4 7.8

Socio-economic level 0.0076
 1 tertile (lowest) 4,656 9,690,079 (32.5) 57.3 34.1 8.6
 2 tertile (middle) 4,701 9,301,266 (31.2) 55.5 36.3 8.2
 3 tertile (highest) 4,609 10,862,262 (36.4) 61.3 31.5 7.2

VG/G – very good/good; B/VB – bad/very/bad.

Table 2.

Characteristics related to health of the population across categories of self-reported general health (estimated population N=29, 853,607).

Variable n N (% weighted) VG/G Moderate B/VB p value
Edentulism 0.0000
 No 12,285 26,801,344 (89.8) 60.0 33.0 7.0
 Yes 1,681 3,052,263 (10.2) 42.8 40.9 16.3

Disability 0.0000
 No 12,449 26,800,380 (89.8) 61.1 32.8 6.2
 Yes 1,517 3,053,227 (10.2) 33.1 43.2 23.6

Physical activity 0.0000
 No 1,139 2,342,223 (7.8) 49.1 32.0 18.9
 Yes 12,827 27,511,384 (92.2) 59.0 34.0 7.0

Chronic disease 0.0000
 No 11,497 24,909,024 (83.4) 63.4 30.6 6.1
 Yes 2,469 4,944,583 (16.6) 32.1 50.2 17.7

BMI 0.0000
 Underweight <18.5 278 528,581 (1.8) 51.7 30.5 17.8
 Normal BMI (18.5–24.9) 5,108 10,884,813 (36.5) 61.1 32.1 6.8
 Overweight (25.0–29.9) 5,820 12,564,208 (42.1) 59.2 33.5 7.4
 Obesity (≥30) 2,760 5,876,005 (19.7) 51.2 38.2 10.6

Smoking (current) 0.9747
 Never 10,872 23,083,604 (77.3) 58.1 33.8 8.1
 Sometimes 1,964 4,592,591 (15.4) 58.9 33.8 7.3
 Daily 1–5 614 1,244,635 (4.2) 58.2 32.8 9.1
 Daily >5 516 932,777 (3.1) 57.7 35.3 7.0

Alcohol use (current) 0.0328
 Never 7,276 15,429,942 (51.7) 59.7 32.8 7.4
 Low 6,393 13,901,545 (46.6) 56.2 35.2 8.6
 High 297 522,120 (1.7) 64.6 27.7 7.8

VG/G – very good/good; B/VB – bad/very/bad.

As for the percentages of the self-reported general health, we noted that the majority (58.2%, N=17,373,754) reported their health status as very good/good, 33.8% (N=10,099,035) said they had a moderate health status, while 8.0% (N=2,380,818) mentioned that their health was bad / very bad.

Bivariate analysis

Tables 1 and 2 show the bivariate distribution of self-reported general health status across the categories of the independent variables included in the study. Table 3 presents the bivariate analysis using polynomial logistic regression (statistically significant variables are presented). We observed that only age, sex, marital status, edentulism, disability, physical activity, presence of chronic disease, BMI, education, occupation, belonging to an indigenous ethnic group, and socioeconomic level were variables significantly associated in the bivariate analysis.

Table 3.

Bivariate multinomial logistic regression analyses for self-rated health and independent variables (only statistically significant results).

Variable Likelihood of moderate vs. good Likelihood of bad/very bad vs. good

OR (95% CI) OR (95% CI)
Age
 35–44 years 1* 1*
 45–59 years 1.58 (1.39–1.81) 2.19 (1.76–2.74)
 60 and more years 2.18 (1.84–2.59) 4.41 (3.18–6.13)

Sex
 Male 1* 1*
 Female 1.38 (1.15–1.65) 1.69 (1.33–2.14)

Marital status
 With partner 1* 1*
 Without partner 1.33 (1.14–1.55) 1.64 (1.31–2.06)

Edentulism
 No 1* 1*
 Yes 1.73 (1.39–2.16) 3.26 (2.51–4.25)

Disability
 No 1* 1*
 Yes 2.43 (1.97–3.00) 7.02 (5.23–9.43)

Physical activity
 No 1* 1*
 Yes 0.88 (0.71–1.10)n/s 0.31 (0.23–0.42)

Chronic disease
 No 1* 1*
 Yes 3.24 (2.75–3.83) 5.75 (4.55–7.28)

BMI
 Underweight <18.5 1.13 (0.74–1.71)n/s 3.10 (1.79–5.37)
 Normal BMI (18.5–24.9) 1* 1*
 Overweight (25.0–29.9) 1.08 (0.91–1.27)n/s 1.12 (0.87–1.44)n/s
 Obesity (≥30) 1.42 (1.20–1.68) 1.87 (1.29–2.69)

Schooling
 Elementary or less 1* 1*
 Complete middle school 0.70 (0.58–0.84) 0.49 (0.35–0.69)
 High School/equivalent 0.54 (0.43–0.68) 0.43 (0.28–0.65)
 College and higher 0.50 (0.37–0.68) 0.28 (0.13–0.58)

Occupation
 Government employee 1* 1*
 Non-government employee 0.84 (0.55–1.29)n/s 1.93 (1.02–3.68)
 Self-employed 1.35 (1.04–1.77) 2.79 (1.65–4.72)
 Does not work/volunteer worker 1.82 (1.38–2.40) 5.61 (3.40–9.24)

Indigenous ethnicity status
 No 1* 1*
 Yes 0.69 (0.49–0.96) 0.83 (0.52–1.33)n/s

Socio-economic level
 1 tertile (lowest) 1* 1*
 2 tertile (middle) 1* 1*
 3 tertile (highest) 0.82 (0.70–0.97) 0.79 (0.62–1.00)n/s
*

Reference category;

n/s

– not significant;

p<0.001;

p<0.01;

p<0.05.

Multivariate model

Table 4 presents the results of the multivariate polynomial logistic regression model; we obtained 11 main effects and an interaction between edentulism and age. Thus, the association of edentulism with self-reported health was modified by age. We can consider: 1) the association of edentulism when age is constant (e.g., 35 years old, which was the minimum age included in the study) on the self-report of moderate health status (OR=exp0.7179=2.05, P=0.194) and of very bad/bad status (OR=exp2.8658=17.56, p<0.001) and 2) the association of edentulism for each year that age increases (e.g., 35–36 years) on the self-reported health with a moderate status (OR=exp0.7179+(−.0090)=2.03, p>0.05) or a very bad/bad status (OR=exp2.8658+(−0.0372)=16.92, p=0.001)) to reach an OR of 1.68 (p=0.001) at 98 years old (which was the maximum age found in the study) in the self-report of health as very bad/bad status. The result for the category moderate was not statistically significant, indicating that the association of edentulism with self-reported health as bad/very bad was higher in young people than in older people, decreasing about 3.6% per each year that age increased. Also, women had higher odds of reporting moderate health (OR=1.35) or bad/very bad health (OR=1.67) compared with men (p<0.05).

Table 4.

Associated variables in the final multinomial logistic regression model for self-rated health.

Variable Likelihood of moderate vs. good Likelihood of bad/very bad vs. good

AOR (CI 95%) AOR (CI 95%)
Edentulism
 No 1* 1*
 Yes 2.05 (0.69–6.08)n/s 17.56 (4.22–73.03)

Age 1.01 (1.01–1.02) 1.02 (1.01–1.03)

Interaction 0.99 (0.97–1.01)n/s 0.96 (0.94–0.98)

Sex
 Male 1* 1*
 Female 1.35 (1.10–1.64) 1.67 (1.31–2.13)

Occupation
 Employed non-manual occupation 1* 1*
 Employed manual occupation 1.27 (1.03–1.56) 1.49 (0.96–2.30)§

Schooling
 Less than college 1* 1*
 College and higher 0.71 (0.60–0.85) 0.62 (0.42–0.90)

Socio-economic level
 1 & 2 tertile (lowest & middle) 1* 1*
 3 tertile (highest) 0.79 (0.68–0.93) 0.71 (0.54–0.93)

Disability
 No 1* 1*
 Yes 1.65 (1.33–2.05) 3.69 (2.73–4.99)

Physical activity
 No 1* 1*
 Yes 1.06 (0.86–1.33)n/s 0.47 (0.34–0.65)

BMI
 Underweight <18.5 1.04 (0.68–1.59)n/s 2.59 (1.42–4.73)
 Normal BMI (18.5–24.9) 1* 1*
 Overweight (25.0–29.9) 1.10 (0.93–1.30)n/s 1.18 (0.91–1.55)n/s
 Obesity (≥30) 1.36 (1.16–1.59) 1.69 (1.11–2.55)

Chronic disease
 No 1* 1*
 Yes 2.65 (2.25–3.12) 3.68 (2.88–4.71)

Alcohol use (current)
 Never 1* 1*
 Low 1.31 (1.13–1.52) 1.59 (1.26–2.00)
 High 1.14 (0.75–1.74)n/s 2.05 (1.00–4.22)§

AOR – Adjusted Odds Ratio by variables contained in the tables.

*

Reference category;

n/s

not significant;

p<0.001;

p<0.01;

p<0.05;

§

p<0.10. The interaction term is explained in the results section.

The results for the socio-economic status indicator variables included in the multivariate model (Table 4) showed that individuals with occupations placed lower in the socioeconomic scale were more likely to report moderate health status (OR=1.27; p<0.05). However, the significance was considered marginal for those who were considered to have bad/very bad health (OR=1.49; p<0.10). On the other hand, having achieved higher levels of education decreased the likelihood of reporting moderate health (OR=0.71) or bad/very bad health (OR=0.62) (p<0.05). Individuals with better socioeconomic position had lower odds of reporting moderate health (OR=0.79) or bad/very bad health (OR=0.71) than their counterparts with lower socioeconomic level (p<0.05).

Table 4 also shows data on health variables. For individuals with a disability, the odds of reporting moderate health were 1.65 times (95% CI=1.33–2.05) compared to individuals without disabilities; this contrast was even starker in those reporting bad/very bad health, 3.69 (95% CI=2.73–4.99). Physical activity was not associated with a moderate health report (p>0.05), however, individuals who had physical activity had lower probabilities of reporting bad/very bad health (OR=0.47, 95% CI=0.34 to 0.65).

Although being underweight or overweight were not associated with a report of moderate health status (p>0.05), obesity itself showed a positive association (OR=1.36, p <0.001). This situation changed when reporting bad/very bad health: when participants were considered underweight (OR=2.59, 95% CI=1.42–4.73) or obese (OR=1.69, 95% CI=1.11–2.55), the odds increased. Being overweight was not significant (p>0.05).

Those who had chronic disease had higher odds of reporting moderate health (OR=2.65; p<0.001), and were even more likely to report having bad/very bad health (OR=3.68; p<0.001).

Finally, low alcohol consumption was associated with a moderate health self-report (OR=1.31; p<0.001); interestingly, high consumption of alcohol was not associated with moderate health (p>0.05). In an analogous way, those who had low alcohol consumption were 59% (p<0.01) more likely to report bad/very bad health, whereas for those with high alcohol consumption, reporting bad/very bad health was marginally significant (OR=2.05; p=0.051).

Discussion

Using national survey data, the present study found that the degree of association between edentulism, socioeconomic status, socio-demographic variables, and the presence of general health problems or disabilities were associated with self-reported general health status among Mexican adults.

Self-evaluations of health generally integrate and synthesize various objective health indicators, its functions, and social and cultural values [21]. We observed a predominance towards health reported as very good/good (58.2%), which was similar to a study in Brazil (60%) [15] but lower than that observed by Laaksonen et al. [4] in Finland, and by Bennet et al. [19] and Jerant et al. [38] in the United States (>70%). In another study performed in Brazil using the same methodology (World Health Survey), the observed percentage of self-reported health as very good/good was 53.3% [16], lower than our figures. In general, the figures for self-reported good/very good health are higher in industrialized than non-industrialized countries.

It is generally accepted that a key element of overall health is oral health. While oral diseases and their sequelae are largely preventable [3944], many adults experience poor oral health [40,41,45]. Although there are no studies that directly link edentulism to self-report of general health, there is evidence of the relationship between deficient oral health and various health conditions and quality of life. For example, in a study conducted in Brazil [46], edentulism was associated with high blood pressure compared to individuals who had more than 10 teeth. In Japan, Aida et al. [47] observed that mortality from cardiovascular disease and respiratory disease was higher among those who had more missing teeth. Recently in Mexico, Medina et al. [29] found that angina pectoris was associated with edentulism. In the U.S., people who reported bad health also indicated having lower quality of life related to oral health [45]. The overall trend from these studies suggests that oral health, specifically tooth loss, is strongly associated with general health. In the case of our study, it should be noted that edentulism was associated with self-reported bad/very bad health (but not on moderate health) depending on age, the effect being greater among young people than in older adults.

In terms of health, the variables of sex (biological construct) and gender (behavioral and social construct) are recognized as useful parameters for research and action, as differences determine specific diseases for men and for women [48]. In this regard, the observed differences between men and women have been well documented by other authors [16,18,20,21], as well as in our own study, with women reporting worse health status than men. One of the main explanations for such a difference is that women may recognize pain and discomfort more easily than men [16]. Other explanations that have been proposed are: 1) the specific conditions of women (maternal conditions, risk exposures, poverty and social exclusion, empowerment), especially in developing countries; 2) conditions associated with increased longevity in women (arising from aging and chronic diseases); 3) conditions resulting from the interaction of sex and gender (depressive symptoms); and 4) gender-based conditions (e.g., violence) [48].

With regard to socioeconomic status, the current literature has documented that the position of an individual in society is generally a strong predictor of both morbidity and mortality. In addition, several authors [49] support the existence of an association between health status and social status: in general, individuals with better socioeconomic status have better health. The results from the present study are consistent with the observed association in other publications about self-reported health and socioeconomic status variables. This relationship has been reported using different indicators [4], such as the highest level of education (schooling) [12,15,18,19,21], poverty level [21], type of occupation [17,22], household size [22], or even renting the residence where people live [15]. In the present study, it was consistently observed in all the three indicator variables that remained in the final model (occupation, education [measured by schooling], and socioeconomic status) that individuals with better socio-economic status reported better health status than those with worse socio-economic status. Among the hypotheses that can explain this association would be access to health services, access to health information, and better nutrition. No definitive interpretation is feasible from the current data.

Self-reported health is a valuable measure in epidemiology because it correlates with present and future morbidity, with different causes of death, and with health services utilization. As a result of several factors, including the aging of the population, a greater proportion of people develop what has been called multimorbidity, with important economic implications [50]. Various authors around the world have found that health conditions are strong predictors of poor overall health at the individual level [21]. Likewise, people with chronic health conditions such as hypertension and diabetes [12,15] or various disabilities [18] reported worse health levels. In the U.S., Ayyagari et al. [6] observed that conditions such as angina, arthritis, congestive heart failure, diabetes and renal disease were associated with worse reported health levels. The results of the present study are consistent with those findings. It is not surprising therefore that certain presentations of BMI (obese individuals) were associated with worse health reports. Similar results have been observed in the U.K. where overweight and obese patients reported worse self-rated health, and more co-morbidities and biological risk factors [23]. A similar situation was found in adults from Brazil [15], as well as in the present study, in that such association was observed only among the obese subjects and not with merely overweight people. However, unlike the Brazilian study, the present study found that individuals characterized as underweight also reported worse general health status.

Like other studies carried out in populations of adolescents [22] and adults [15,18,24], the results of the present study showed that physical activity may be a protective factor against self-reported poor health. A sedentary lifestyle and irregular physical exercise have been previously associated with self-reported poor health in Mexican women [12]. According to the WHO, physical inactivity is the fourth leading risk factor affecting overall mortality, and is the cause of almost 6% of all deaths. It is generally accepted that physical activity is an important element of a healthy lifestyle – it improves lipid profile, blood pressure, metabolic syndrome, muscle strength and bone density, and is associated with a reduction in excess weight, emotional problems, and depressive symptoms [22,51].

Numerous studies have explored the relationship between alcohol consumption and health. Compared with abstention, moderate alcohol consumption has been linked to better health, including subjective health. On the other hand, excessive and harmful consumption of alcohol is associated with increased morbidity and mortality [15,25,26]. Green and Pollen [25] mentioned that studies relating alcohol to health have failed to take into account the possible heterogeneity in health history and alcohol consumption among non-drinkers and former drinkers, by combining them with lifetime abstainers in the analysis. To the extent that former drinkers stop drinking due to illness, this could increase the risk of the non-drinking category and underestimate the adverse effects of alcohol consumption on health; diseases that lead to abstention are related to alcohol. In our study, those who had low alcohol consumption in the previous week had a higher risk of reporting moderate and bad/very bad health, along with the strong tendency to select the category of bad/very bad health. These differences could be due to methodological issues, such as the fact that in our study alcohol consumption was measured only for the previous week without taking into account the former drinkers’ history; whereas in other studies the time base was between 6–12 months. Besides the different epidemiological designs used in other studies and in ours, it is possible [52] that by collapsing categories of those who currently drink no alcohol, we may be in fact combining people who are no longer using alcohol after substantial abuse with life-long abstainers.

The present study has limitations and strengths that should be taken into consideration when analyzing conclusions. The main limitation is the inability to pinpoint causality between different variables, which is an inherent weakness in cross-sectional studies. However, the ENED provided reliable and internationally comparable information about a wide variety of health indicators, including measures of general health of the population and the effectiveness of health systems. Our data represent most of the country’s adult population, and our study provides an initial assessment of the importance of complete loss of teeth in the context of self-perception of general health.

Conclusions

The association between edentulism and self-reported poor health status (bad/very bad) in the Mexican adult population was stronger in the younger segment of the population studied. We observed not only socioeconomic inequalities in relation to the self-report of general health, but also that people with a chronic illness or a disability reported their perceived general health status as less favorable.

Footnotes

Conflict of interest statement

None.

Source of support: Publication supported by the Ministry of Education, Mexican Federal Government, through of The Faculty Improvement Program (PROMEP)

References

  • 1.Salinas-Martínez A, Muñoz-Moreno F, Barraza de León AR, et al. [Health needs in primary care diabetic clients]. Salud Publica Mex. 2001;43:324–35. [PubMed] [Google Scholar]
  • 2.Schlaepfer-Pedrazzini L, Infante-Castañeda C. [Measuring health: Methodological and theoretical perspectives]. Salud Publica Mex. 1990;32:141–55. [PubMed] [Google Scholar]
  • 3.Eriksson I, Unden AL, Elofsson S. Self-rated health. Comparisons between three different measures. Results from a population study. Int J Epidemiol. 2001;30:326–33. doi: 10.1093/ije/30.2.326. [DOI] [PubMed] [Google Scholar]
  • 4.Laaksonen M, Rahkonen O, Martikainen P, Lahelma E. Socioeconomic position and self-rated health: the contribution of childhood socioeconomic circumstances, adult socioeconomic status, and material resources. Am J Public Health. 2005;95:1403–9. doi: 10.2105/AJPH.2004.047969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Bayliss EA, Ellis JL, Shoup JA, et al. Association of patient-centered outcomes with patient-reported and ICD-9-based morbidity measures. Ann Fam Med. 2012;10:126–33. doi: 10.1370/afm.1364. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Ayyagari P, Ullrich F, Malmstrom TK, et al. Self-rated health trajectories in the African American health cohort. PLoS One. 2012;7:e53278. doi: 10.1371/journal.pone.0053278. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Perruccio AV, Katz JN, Losina E. Health burden in chronic disease: Multimorbidity is associated with self-rated health more than medical comorbidity alone. J Clin Epidemiol. 2012;65:100–6. doi: 10.1016/j.jclinepi.2011.04.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Latham K, Peek CW. Self-rated health and morbidity onset among late midlife U.S. adults. J Gerontol B Psychol Sci Soc Sci. 2013;68:107–16. doi: 10.1093/geronb/gbs104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Hirve S, Juvekar S, Sambhudas S, et al. Does self-rated health predict death in adults aged 50 years and above in India? Evidence from a rural population under health and demographic surveillance. Int J Epidemiol. 2012;41:1719–27. doi: 10.1093/ije/dys163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Tiainen K, Luukkaala T, Hervonen A, Jylhä M. Predictors of mortality in men and women aged 90 and older: a nine-year follow-up study in the Vitality 90+ study. Age Ageing. 2013;42:468–75. doi: 10.1093/ageing/aft030. [DOI] [PubMed] [Google Scholar]
  • 11.Smith KV, Goldman N. Socioeconomic differences in health among older adults in Mexico. Soc Sci Med. 2007;65:1372–85. doi: 10.1016/j.socscimed.2007.05.023. [DOI] [PubMed] [Google Scholar]
  • 12.Vladislavovna-Doubova S, Pérez-Cuevas R, Reyes-Morales H. [Self-rated health among climacteric women affiliated with the Instituto Mexicano del Seguro Social]. Salud Publica Mex. 2008;50:390–96. doi: 10.1590/s0036-36342008000500012. [DOI] [PubMed] [Google Scholar]
  • 13.Valle AM. Social class, marginality and self-assessed health: a cross-sectional analysis of the health gradient in Mexico. Int J Equity Health. 2009;8:3. doi: 10.1186/1475-9276-8-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Ortiz-Hernández L, Tello BL, Valdés J. The association of sexual orientation with self-rated health, and cigarette and alcohol use in Mexican adolescents and youths. Soc Sci Med. 2009;69:85–93. doi: 10.1016/j.socscimed.2009.03.028. [DOI] [PubMed] [Google Scholar]
  • 15.Pavão AL, Werneck GL, Campos MR. [Self-rated health and the association with social and demographic factors, health behavior, and morbidity: a national health survey]. Cad Saude Publica. 2013;29:723–34. [PubMed] [Google Scholar]
  • 16.Szwarcwald CL, Souza-Júnior PR, Esteves MA, et al. Socio-demographic determinants of self-rated health in Brazil. Cad Saude Publica. 2005;21(Suppl):54–64. doi: 10.1590/s0102-311x2005000700007. [DOI] [PubMed] [Google Scholar]
  • 17.McFadden E, Luben R, Bingham S, et al. Social inequalities in self-rated health by age: cross-sectional study of 22,457 middle-aged men and women. BMC Public Health. 2008;8:230. doi: 10.1186/1471-2458-8-230. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Darviri C, Fouka G, Gnardellis C, et al. Determinants of self-rated health in a representative sample of a rural population: a cross-sectional study in Greece. Int J Environ Res Public Health. 2012;9:943–54. doi: 10.3390/ijerph9030943. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Bennett IM, Chen J, Soroui JS, White S. The contribution of health literacy to disparities in self-rated health status and preventive health behaviors in older adults. Ann Fam Med. 2009;7:204–11. doi: 10.1370/afm.940. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Setia MS, Lynch J, Abrahamowicz M, et al. Self-rated health in Canadian immigrants: analysis of the Longitudinal Survey of Immigrants to Canada. Health Place. 2011;17:658–70. doi: 10.1016/j.healthplace.2011.01.006. [DOI] [PubMed] [Google Scholar]
  • 21.Todorova IL, Tucker KL, Jimenez MP, et al. Determinants of self-rated health and the role of acculturation: implications for health inequalities. Ethn Health. 2013;18(6):563–85. doi: 10.1080/13557858.2013.771147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Galán I, Boix R, Medrano MJ, et al. Physical activity and self-reported health status among adolescents: a cross-sectional population-based study. BMJ Open. 2013;3:e002644. doi: 10.1136/bmjopen-2013-002644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hamer M, Stamatakis E. Overweight and obese cardiac patients have better prognosis despite reporting worse perceived health and more conventional risk factors. Prev Med. 2013;57:12–16. doi: 10.1016/j.ypmed.2013.02.012. [DOI] [PubMed] [Google Scholar]
  • 24.Södergren M, McNaughton SA, Salmon J, et al. Associations between fruit and vegetable intake, leisure-time physical activity, sitting time and self-rated health among older adults: cross-sectional data from the WELL study. BMC Public Health. 2012;12:551. doi: 10.1186/1471-2458-12-551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Green CA, Polen MR. The health and health behaviors of people who do not drink alcohol. Am J Prev Med. 2001;21:298–305. doi: 10.1016/s0749-3797(01)00365-8. [DOI] [PubMed] [Google Scholar]
  • 26.Pisinger C, Toft U, Aadahl M, et al. The relationship between lifestyle and self-reported health in a general population: the Inter99 study. Prev Med. 2009;49:418–23. doi: 10.1016/j.ypmed.2009.08.011. [DOI] [PubMed] [Google Scholar]
  • 27.Medina-Solis CE, Pérez-Núñez R, Maupomé G, Casanova-Rosado JF. Edentulism among Mexicans 35 years old and older, and associated factors. Am J Public Health. 2006;96:1578–81. doi: 10.2105/AJPH.2005.071209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Medina-Solís CE, Pérez-Núñez R, Maupomé G, et al. National survey on edentulism and its geographic distribution, among Mexicans 18 years of age and older (with emphasis in WHO age groups) J Oral Rehabil. 2008;35:237–44. doi: 10.1111/j.1365-2842.2007.01767.x. [DOI] [PubMed] [Google Scholar]
  • 29.Medina-Solís CE, Pontigo-Loyola AP, Pérez-Campos E, et al. Association between edentulism and angina pectoris in Mexican adults 35 years of age and older: A multivariate analysis of a population-based survey. J Periodontol. 2014;85(3):406–16. doi: 10.1902/jop.2013.130186. [DOI] [PubMed] [Google Scholar]
  • 30.Pérez-Núñez R, Medina-Solis CE, Maupomé G, Vargas-Palacios A. Factors associated with dental health care coverage in Mexico: Findings from the National Performance Evaluation Survey 2002–2003. Community Dent Oral Epidemiol. 2006;34:387–97. doi: 10.1111/j.1600-0528.2006.00289.x. [DOI] [PubMed] [Google Scholar]
  • 31.World Health Organization. World Health Survey [serial on the Internet] [Accessed April 28, 2013]. Available at: http://www.who.int/healthinfo/survey/en/
  • 32.Vinson DC, Turner BJ, Manning BK, Galliher JM. Clinician suspicion of an alcohol problem: an observational study from the AAFP National Research Network. Ann Fam Med. 2013;11:53–59. doi: 10.1370/afm.1464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Gutierrez JP, Rivera-Dommarco J, Shamah-Levy T, et al. National Health and Nutrition Survey 2012. National results. Cuernavaca, Mexico: Instituto Nacional de Salud Publica (MX); 2012. [Google Scholar]
  • 34.Kolenikov S, Angeles G. Working paper No. WP-04-85. Chapel Hill: CPC/MEASURE; 2004. The use of discrete data in Principal Component Analysis with applications to socio-economic indices; pp. 1–59. [Google Scholar]
  • 35.McKnight PE, McKnight KM, Sidani S, Figueredo AJ. Missing data: A gentle introduction. New York: Guilford; 2007. [Google Scholar]
  • 36.Ananth CV, Kleinbaum DG. Regression models for ordinal responses: a review of methods and applications. Int J Epidemiol. 1997;26:1323–33. doi: 10.1093/ije/26.6.1323. [DOI] [PubMed] [Google Scholar]
  • 37.Hosmer DW, Lemeshow S. Applied logistic regression. 2nd ed. New York: Jonh Wiley & Sons Interscience Publication; 2000. [Google Scholar]
  • 38.Jerant A, Bertakis KD, Fenton JJ, Franks P. Extended office hours and health care expenditures: a national study. Ann Fam Med. 2012;10:388–95. doi: 10.1370/afm.1382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Medina-Solís CE, Pontigo-Loyola AP, Mendoza-Rodríguez M, et al. Treatment needs for dental caries, restorative care index, and index of extractions in adolescents 12 to 15 years old. West Indian Med J. 2013;62:636–41. doi: 10.7727/wimj.2012.300. [DOI] [PubMed] [Google Scholar]
  • 40.Medina-Solís CE, Pontigo-Loyola AP, Pérez-Campos E, et al. [Principal reasons for extraction of permanent tooth in a sample of Mexicans adults]. Rev Invest Clin. 2013;65:141–49. [PubMed] [Google Scholar]
  • 41.Ma H, Shi XC, Hu DY, Li X. The poor oral health status of former heroin users treated with methadone in a Chinese city. Med Sci Monit. 2012;18(4):PH51–55. doi: 10.12659/MSM.882611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.del Herrera MS, Medina-Solís CE, Minaya-Sánchez M, et al. Dental plaque, preventive care, and tooth brushing associated with dental caries in primary teeth in schoolchildren ages 6–9 years of Leon, Nicaragua. Med Sci Monit. 2013;19:1019–26. doi: 10.12659/MSM.884025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Zuñiga-Manriquez AG, Medina-Solís CE, Lara-Carrillo E, et al. Experiencia, prevalencia y severidad de caries dental asociada con el estado nutricional en infantes mexicanos de 17 a 47 meses de edad. Rev Invest Clin. 2013;65:228–36. [PubMed] [Google Scholar]
  • 44.Hernández-Martínez CT, Medina-Solís CE, Robles-Bermeo NL, et al. [Oral hygiene customs across age and sex in 6–12 years schoolchildren]. Rev Invest Clin. 2014 [in press] [PubMed] [Google Scholar]
  • 45.Griffin SO, Jones JA, Brunson D, et al. Burden of oral disease among older adults and implications for public health priorities. Am J Public Health. 2012;102:411–18. doi: 10.2105/AJPH.2011.300362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Peres MA, Tsakos G, Barbato PR, et al. Tooth loss is associated with increased blood pressure in adults – a multidisciplinary population-based study. J Clin Periodontol. 2012;39:824–33. doi: 10.1111/j.1600-051X.2012.01916.x. [DOI] [PubMed] [Google Scholar]
  • 47.Aida J, Kondo K, Yamamoto T, et al. Oral health and cancer, cardiovascular, and respiratory mortality of Japanese. J Dent Res. 2011;90:1129–35. doi: 10.1177/0022034511414423. [DOI] [PubMed] [Google Scholar]
  • 48.Buvinić M, Medici A, Fernández E, Torres AC. Gender Differentials in Health. In: Jamison DT, Breman JG, Measham AR, et al., editors. Disease Control Priorities in Developing Countries. 2nd ed. Washington (DC): World Bank; 2006. [Google Scholar]
  • 49.Kawachi I. Income inequality in Health. In: Berkman L, Kawachi I, editors. Social Epidemiology. New York: Oxford University Press; 2000. pp. 76–93. [Google Scholar]
  • 50.Fortin M, Stewart M, Poitras ME, et al. A systematic review of prevalence studies on multimorbidity: toward a more uniform methodology. Ann Fam Med. 2012;10:142–51. doi: 10.1370/afm.1337. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Chatton A, Kayser B. Self-reported health, physical activity and socio-economic status of middle-aged and elderly participants to a popular road running race in Switzerland: better off than the general population? Swiss Med Wkly. 2013;143:w13710. doi: 10.4414/smw.2013.13710. [DOI] [PubMed] [Google Scholar]
  • 52.Liang W, Chikritzhs T. The association between alcohol exposure and self-reported health status: the effect of separating former and current drinkers. PLoS One. 2013;8:e55881. doi: 10.1371/journal.pone.0055881. [DOI] [PMC free article] [PubMed] [Google Scholar]

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