Abstract
Do self-evaluations of general health change as individuals age? Although several perspectives point to age-related shifts, few researchers have compared them. For this article, several competing hypotheses were tested using a large, nationally representative, and longitudinal data set. The results suggest two trends. First, the correspondence between functional limitations and self-rated health declines, especially after age 50. Similarly, the correspondence between various chronic conditions and self-rated health declines with age. These findings are consistent with social comparison theory. Yet, the results also suggest that the correspondence between depressive symptoms and self-rated health increases. Indeed, after age 74, the correspondence between self-rated health and some common symptoms of depression becomes stronger than that between self-rated health and several chronic, and often fatal, somatic conditions. This crossover has important implications for the detection and treatment of depressive symptoms in later life.
Keywords: Self-rated health, depression, aging
Self-evaluations of general health are among the most widely used measures of health status in research on the need for and outcomes of medical care. The popularity of such evaluations—referred to in this article as “self-rated health”—reflects two things. First, self-rated health is easy to include in surveys, and item nonresponse is consistently low. Respondents are simply asked to rate their health from “excellent” to “poor” and have little obvious difficulty doing so. Self-rated health has been a cornerstone to such well-known and influential studies and surveys as the National Health Interview Survey, the Medical Outcomes Study, and the RAND Health Insurance Experiment. Second, self-rated health has a number of desirable empirical qualities. For one, it predicts mortality exceptionally well, usually better than and independent of a wide array of disease-specific indicators (Ferraro and Farmer 1999; Idler and Benyamini 1997; Kaplan and Camacho 1983). It also anticipates treatment behavior and is important to evaluating patient outcomes. Indeed, most models of health care utilization are premised on perceptions of general health (e.g., Rosenstock 1966). Furthermore, most researchers now recognize that perceptions of general health reflect patients’ symptoms and values and thus are central to patients’ reports of health-related quality of life (Cleary and Edgman-Levitan 1997; Patrick and Erickson 1993; Wilson and Cleary 1995).
Yet despite the popularity, validity, and conceptual appeal of self-rated health, researchers remain uncertain about its psychological underpinnings. Earlier studies examined the meaning of self-rated health by exploring its relationship to a variety of particular indicators (e.g., diagnoses) (Harlow and Linet 1989; Pijls, Feskens, and Kromhout 1993) or by asking a small group of study participants to elaborate on their concept of “health” (Krause and Jay 1994). These studies reveal the great breadth of referents that individuals consider when asked to evaluate their health globally, from mental health to physical health to functional limitations. Furthermore, they show that these evaluations incorporate the individual's preferences and experiences (Jylhä et al. 2001). Nevertheless, numerous gaps remain. Among the most important is that few studies have explicitly tried to determine when self-evaluations of general health begin to diverge from more particular indicators. Although researchers are careful to distinguish self-evaluations of health from clinical outcome measures, they generally emphasize the strong relationship between the two. Indeed, the value of self-rated health to researchers now seems to derive more from its convenient overlap with a variety of “objective” indicators than from what it reveals about a person's unique construal of his or her health. In short, self-rated health is often equated with health itself.
This article tries to recapture the subjectivity of self-rated health by opening the black box of what it measures. Moreover, as an extension of previous research, this article examines how evaluations of health change with age. It focuses on age for several reasons. First, a number of theoretical frameworks anticipate—explicitly or implicitly—that age affects how health is evaluated (for a review, see the special issue of Research on Aging, May 1999) (Harlow and Linet 1989; Pijls, Feskens, and Kromhout 1993; Suls, Marco, and Tobin 1991). Indeed, research suggests that age may affect evaluations of health more than does any other sociodemographic characteristic (Krause and Jay 1994). A focus on age may also help shed additional light on issues of special significance to contemporary clinical practice. Understanding the basis for the aged's self-evaluations of general health is important to those interested in meeting their health care needs.
I explore these issues using a nationally representative longitudinal data set with an extensive battery of health-related questions (Americans’ Changing Lives, House 2003). Employing methods similar to those used for other sociodemographic characteristics (regarding gender, see Case and Paxson 2005), I examine the associations between self-rated health and various health indicators and how these associations change with age. The data had two advantages.
First, the longitudinal design allowed me to test age-based interpretations against equally viable cohort-based interpretations. Most of the theories I discuss emphasize how perceptions of health change with age. For example, social comparison theory argues that as individuals age, they are more likely to witness the poor health of their peers and to adjust their evaluations of their own health accordingly. Other perspectives emphasize cohort. Beliefs about health and illness may be formed—as are many beliefs—early in life. Recent cohorts may hold higher expectations for good health, and these expectations may shape the perceived severity of assorted health-related limitations and elevate the severity of conditions that earlier cohorts considered minor.
Second, the extensive battery of health questions allowed me to examine the numerous and varied components of self-rated health. The results point to dramatic shifts in the psychological underpinnings of self-rated health, shifts that are at once consistent and inconsistent with previous speculation.
Background
Social Comparison or Illness Preoccupation
Nearly all accounts of self-rated health begin with the idea that health is evaluated relative to the health of comparable others and that individuals may be “biased” toward making favorable comparisons. In a series of now-classic studies, Wood, Taylor, and Lichtman (1985) demonstrated that when asked to evaluate the severity of their condition, women with breast cancer were more likely to compare themselves with women whose condition was worse than their own than with women whose condition was better (i.e., they were more likely to make “downward” rather than “upward” comparisons). A similar result was documented for other illnesses of similar or lesser severity (Afflect et al. 1988; DeVellis et al. 1990; Helgeson and Taylor 1993), thus leading researchers to the more general conclusion that individuals often are motivated to allay the perceived threat of illness more than they are to seek completely objective and accurate information.1 This idea suggests that the elderly may be especially apt to inflate their self-evaluations of health, given that they have more opportunities to make downward comparisons among their peers. To this point, research already indicates that individuals act as lay epidemiologists and evaluate the severity of a condition based on how unusual they believe it is for someone their age (Croyle 1992; Suls, Marco, and Tobin 1991). Furthermore, a good deal of research finds that the elderly rate their health in a seemingly optimistic fashion. Using open-ended interviews, Idler (1993) found that many elderly report having good overall health, even though they also are quick to note that they have good health despite some limitations. Similarly, quantitative studies revealed that the correlation between functional limitations and self-rated health loosened in later life, precisely when such limitations become more prevalent and severe (Hoeymans et al. 1997; Levkoff, Cleary, and Wetle 1987).
Although social comparison has received some generic support, there are reasons to expect that the salience of illness increases with age. The elderly might simply be more aware of illness, and this awareness might, in turn, be sufficient to prompt perceptions of poor general health. Leventhal (1984) elaborated a cognitive model of illness perception. In this model, physical limitations and diagnosed health problems cue other symptoms and limitations that might otherwise have been overlooked but, once recognized through the lens of a diagnosis, bolster a more general sense of failing health. This model predicts that the correlation between any particular health indicator and self-evaluations of general health will increase with age. Although very much at odds with the predictions of social comparison, this model has received at least some empirical support. For example, Strain (1993) found a steady increase in the salience of functional limitations with age; Krause and Jay (1994) found that older persons were more likely than younger persons to consider specific health problems when evaluating their health; and several researchers documented health pessimism among the elderly (Borawski, Kinney, and Kahana 1996; Goldstein, Siegel, and Boyer 1984; Idler, Hudson, and Leventhal 1999; Levkoff, Cleary, and Wetle 1987). More generally, the model is consistent with the finding that the elderly seek health care quickly in response to any symptom that they regard as even moderately threatening, a response premised on a growing sense of health-related vulnerability (Leventhal et al. 1993).
The Case of Depression
It is important to distinguish mental health from physical health, as the two may follow very different age trajectories. Indeed, it is unclear whether depressive symptoms are considered in self-assessments of general health at all: some studies found that when asked to discuss their health, very few people make explicit spontaneous references to mental health (Krause and Jay 1994). On the one hand, we might expect that the salience of depressive symptoms for self-evaluations of health would decline with age. The undertreatment of depression among the elderly is a widely recognized problem and may be rooted in the elderly's belief that depression is an inevitable part of aging, loss, and grief (see Unützer et al. 1999). These beliefs may be exacerbated by physicians’ behavior insofar as they do not feel that depression warrants any additional investigation or treatment beyond that provided for chronic illness (Glasser and Gravdal 1997).
Yet on the other hand, there are good reasons to expect that the elderly are concerned with emotional experiences, even if they do not articulate such experiences in terms of depression. Along these lines, socioemotional selectivity theory argues that motives change considerably with age (Carstensen, Isaacowitz, and Charles 1999). The theory predicts that as individuals age, their time horizons become shorter, and they begin to devote more attention to realizing emotional satisfaction in the present than to making behavioral investments for the future. Although this theory has not been applied to self-rated health, its insights can easily be generalized. Several studies speak to the growing importance of emotions with age. For example, the elderly appear to weigh the avoidance of negative emotions more strongly than do the young when making decisions about social activities (Blanchard-Fields 1986; Blanchard-Fields, Jahnke, and Camp 1995). Indeed, recent studies of health-related quality of life are entirely consistent with the theory's predictions. In a study of adults with coronary artery disease, Ruo and colleagues (2003) discovered that depressive symptoms were strongly associated with patient-reported global health status but that two physiological measures of disease severity—left ventricular rejection fraction and ischemia—were not. Because of the restricted age range of the study's participants (whose average age was over 60), the authors were unable to address age-related differences in the relationship between depressive symptoms and global health. Nevertheless, socioemotional selectivity theory anticipates these results and further predicts that they may be particular to an older-age sample.
Limitations of Previous Research
The complex results of these studies reflect many things, but they undoubtedly reflect, at least in part, the diverse methods that the studies employ. This is an area in which qualitative research—with some notable exceptions—has far outweighed survey research. Although qualitative research is useful for uncovering the many components underlying self-rated health, it is less useful for evaluating the relative strengths of these assorted components. Furthermore, although interested in age, many of these studies are cross-sectional and so are unable to disentangle age from cohort (Borawski, Kinney, and Kahana 1996; Goldstein, Siegel, and Boyer 1984; Hoeymans et al. 1997; Idler 1993; Idler, Hudson, and Leventhal 1999; Johnson and Wolinsky 1993; Levkoff, Cleary, and Wetle 1987; Maddox and Douglass 1973; Mechanic and Angel 1987; Rakowski and Cryan 1990; Tornstam 1975). This is an especially important limitation given that nearly all the preceding findings could be interpreted in terms of cohort. Recent cohorts may have different conceptions of health given the currently longer life expectancy, improvements in medical treatment, and broad public enthusiasm for medical enhancement (Flykesnes and Forde 1991; Rosenberg 2002; Starr 1982). Along these lines, Spiers and colleagues (1996) found that recent cohorts in England and Wales were more likely to include mild conditions in their self-evaluations of health, findings they interpreted in terms of these cohorts’ especially strong expectations for a healthy life.
Data and Methods
Americans’ Changing Lives (ACL) provides an excellent opportunity to redress many of these limitations (House 2003). The ACL is a nationally representative longitudinal study of adults aged 25 and older and is widely used in medical sociology and other disciplines. Respondents were identified using a four-stage sampling strategy, beginning with standard metropolitan statistical areas and counties, followed by smaller geographic areas, followed by houses, and, last, a random selection of eligible respondents. The ACL followed an initial sample for three waves (1986, 1989, and 1994). In the first wave, 3,617 respondents were interviewed, with an overall response rate of 68 percent. An attempt was made to recontact all these respondents in the second and third waves, although the sample size shrank somewhat over time. With nonresponse and mortality (corresponding to a loss of 584 and 166 respondents, respectively), 2,867 respondents were interviewed in the second wave, and following similar patterns of attrition, 2,562 respondents were interviewed in the third. The ACL oversampled African Americans and those over the age of 60.2 It also contains numerous indicators of morbidity.
Morbidity Indicators
The dependent variable in the following regression models is self-rated health. The question about self-rated health was “How would you rate your health at the present time? Would you say it is excellent [coded as 1], very good, good, fair, or poor [coded as 5]?”3 Although this direction of coding is the reverse of that used in most other studies, it provides a more straightforward way of evaluating a growing association between a particular condition and self-rated health, as a growing association will be realized in a positive increase in an already positive coefficient. The age groups were divided into one of six categories (see House et al. 1994): 25 to 34, 35 to 44, 45 to 54, 55 to 64, 65 to 74, and 75 and older. The ACL contains three types of morbidity indicators.
Chronic Somatic Conditions
The respondents were asked whether they had experienced each of the following conditions in the previous twelve months: arthritis or rheumatism, stroke, cancer or a malignant tumor, diabetes or high blood sugar, heart attack or other heart trouble, hypertension, and lung disease. Each condition was coded as a yes (1) or no (0) dummy variable.
Functional Limitations
The respondents also were asked a series of questions about functional limitations, in five domains: the degree of difficulty they had in bathing themselves; whether they had difficulty climbing stairs, walking several blocks, and doing heavy housework; and if they were in a bed or chair all or most of the day. Responses to these items were combined to create a four-level Guttman-style scale (ranging from 1 to 4) (Guttman 1950), with the first level indicating no functional limitations; the second indicating difficulty with heavy housework; the third indicating difficulty climbing stairs or walking; and the fourth indicating those who were in a bed or chair most of the day and/or had difficulty bathing. Because the distance between adjacent levels is unknown and may not be constant, the association between self-rated health and the functional limitations scale is estimated using a series of three dummy variables (with “no impairment” as the reference category).
The Center for Epidemiological Studies Depression Scale (CES-D)
The CES-D is one of the most popular dimensional measure of depressive symptoms in the social sciences (Radloff 1977). The shortened version of the CES-D contained in the ACL consists of 11 items. The respondents were asked whether they experienced the following symptoms “hardly ever” (coded 1), “some of the time,” or “most of the time” (coded 3) during the past week: “I felt depressed,” “I felt that everything I did was an effort,” “My sleep was restless,” “I was happy”[reverse coded for scale construction], “I felt lonely,” “People were unfriendly,” “I enjoyed life”[reverse coded], “I did not feel like eating. My appetite was poor,” “I felt sad,” “I felt that people disliked me,” and “I could not get going.” The analyses use these diverse items in two different ways. The models presented in Tables 3 and 4 used a standardized average, with a mean of zero and a variance of one: tests of coefficient reliability were sufficiently high for a summary measure (alpha = .83) (Cronbach 1951). The models presented in Table 6 explored each of the 11 items separately in order to examine the comparability of results between the affective items (e.g., “I felt sad”) and the somatic items (e.g., “I did not feel like eating”).
TABLE 3.
Coefficients from Six Age-Stratified Regressions of Self-Rated Health on Depressive Symptoms (CES-D): Americans’ Changing Lives, 1986
| Age Group | ||||||
|---|---|---|---|---|---|---|
| 25–34 | 35–44 | 45–54 | 55–64 | 65–74 | 75+ | |
| Depressive symptoms, | 0.236 | 0.305 | 0.376 | 0.468 | 0.437 | 0.472a |
| CES-D | (0.032) | (0.034) | (0.052) | (0.038) | (0.038) | (0.048) |
| N | 740 | 591 | 390 | 685 | 765 | 446 |
| CES-D mean | 088 | 019 | −.066 | −.089 | −.141 | 138 |
| (standardized) | ||||||
Note: All coefficients from models regressing self-rated health on CES-D and race/ethnicity (coefficients for race/ethnicity not shown). Standard errors are in parentheses. All coefficients significantly different from zero at p < .05.
Test of linear trend between age groups (i.e., age × illness interactions) significant at p < .05.
TABLE 4.
Random- and Fixed-Effects Regressions of Self-Rated Health on Depressive Symptoms (CES-D) × Age Interactions: Americans’ Changing Lives, 1986, 1989, 1994
| Model 1 Random Effects | Model 2 Random Effects | Model 3 Fixed Effects | Model 4 Random Effects, Survivor Sample | |
|---|---|---|---|---|
| Depressive symptoms, | 0.094b | 0.108b | 0.058 | 0.114b |
| CES-D | (0.033) | (0.030) | (0.043) | (0.035) |
| Age | 0.019b | 0.003b | 0.030b | 0.018b |
| (0.001) | (0.001) | (0.003) | (0.001) | |
| Depressive symptoms, | 0.004b | 0.0014a | 0.002a | 0.003b |
| CES-D × age | (0.001) | (0.0005) | (0.001) | (0.001) |
| Functional limitations (vs. no impairment) | ||||
| Least severe | 0.465b | |||
| impairment | (0.032) | |||
| Moderately severe | 0.735b | |||
| impairment | (0.038) | |||
| Most severe | 0.783b | |||
| impairment | (0.043) | |||
| Number of chronic | 0.232b | |||
| conditions | (0.009) | |||
| Constant | 1.447b | 1.898b | 0.923b | 1.491b |
| Total N | 8,881 | 8,881 | 8,881 | 8,053 |
| Individuals | 3,617 | 3,617 | 3,617 | 3,071 |
Note: Random-effects models also include controls for race/ethnicity (coefficients not shown). Survivor sample consists of respondents who survived for all three panels of observation.
p < .05.
p < .01 (standard errors in parentheses).
TABLE 6.
Coefficients from 11 Regressions of Self-Rated Health on Depressive Symptoms among Respondents Ages 75 and Older: Americans’ Changing Lives, 1986 (N = 446)
| Model and Independent Variable | Some of the Time (vs. Hardly Ever) | Most of the Time (vs. Hardly Ever) |
|---|---|---|
| 1. I felt depressed. | 634a | 877a |
| (.115) | (.236) | |
| 2. I felt that everything | 623a | 1.180a |
| I did was an effort. | (.110) | (.165) |
| 3. My sleep was restless. | 446a | 713a |
| (.116) | (.156) | |
| 4. I was happy. | 136 | −.597a |
| (.195) | (.178) | |
| 5. I felt lonely. | 405a | 710a |
| (.119) | (.190) | |
| 6. People were unfriendly. | 530a | 667a |
| (.177) | (.244) | |
| 7. I enjoyed life. | 300 | −.691a |
| (.204) | (.178) | |
| 8. I did not feel like eating. | 746a | 620a |
| (.118) | (.198) | |
| 9. I felt sad. | 573a | 409 |
| (.117) | (.213) | |
| 10. I felt that people disliked me. | 340 | 589 |
| (.190) | (.312) | |
| 11. I could not get going. | 550a | 1.013a |
| (.111) | (.178) |
Note: Coefficients are from eleven models regressing self-rated health on each symptom of depression and race/ethnicity (coefficients for race/ethnicity not shown).
p < .01 (standard errors in parentheses).
Statistical Strategy
Recall that the ACL is a panel survey. Two types of models are used, each with a different goal in mind. First, simple linear regression models are used in order to examine the association between particular health indicators and self-rated health.4 In these cross-sectional models, self-rated health is regressed on each of the particular indicators, using observations from the first panel only. Second, the models use data from all three panels (with person panels as the unit of observation) in order to test the sensitivity of the cross-sectional models to cohort-based processes. In this series of models, both random- and fixed-effects models are estimated. Random-effects regression models are similar to linear regression models but correct for the within-person correlation resulting from using multiple observations from a single person (Baltagi 1995). Fixed-effects regression models, by contrast, consider these multiple observations by estimating (or by conditioning out of the estimation process) a constant (or “fixed”) parameter for each individual (Allison 1990; England et al. 1988). Because fixed-effects models include an individual-specific constant, they are able to estimate coefficients only for those variables that change between panels. But by focusing on change, such models eliminate from consideration all of an individual's observed and unobserved unchanging characteristics.5 This property is attractive to social scientists because it provides a convenient solution to the common problem of unobserved heterogeneity. In my study, it offered a simple way to test the sensitivity of age effects to cohort.
Cohort effects are, by definition, fixed—they pertain to beliefs developed at particular historical periods and at particular times during life, usually in early formative years, which then are carried forward. To be sure, fixed-effects models do not completely resolve the cohort problem: they do not eliminate interactions between age and cohort (see Ryder 1965), and because the ACL covers only eight years, they are less sensitive to age-related change than are data observed over a longer period. Nevertheless, fixed-effects models provide a convenient and useful sensitivity analysis: if age-group differences reflect cohort differences instead, the use of fixed-effects models should eliminate (or substantially reduce) the effects of age.
The results begin with three tables that examine the simple association between self-rated health and the three types of particular health-related evaluations as outlined earlier. Although the models may appear underspecified, it is important to reiterate that this study is concerned with the association between self-rated health and more particular indicators (e.g., education, income, occupation). It is not concerned with the epidemiological causes of health. Including variables antecedent to both self-rated health and more particular indicators would reduce the coefficients for the health indicators but would not shed any additional light on the debates with which this study is concerned.
Results
Table 1 presents coefficients from 39 regressions of self-rated health on each of seven chronic conditions, stratified by age group (because of the small sample size, the models could not be estimated for stroke among those under the age of 55). For each condition, the first row presents the coefficient, followed in the second row by the standard error, and, in the third row, by the condition's prevalence. Although not denoted using the conventional asterisks for statistical significance, each of the coefficients is statistically significant from zero at p < .05. The coefficients show the strength of the relationship between reports of a condition, such as arthritis or cancer, and self-assessments of general health: the larger the coefficient is, the stronger the relationship. Thus, for example, reporting having cancer is more strongly associated with self-rated health for those ages 25 to 34 than for any other age group. By examining patterns between age groups, it is possible to test the preceding hypotheses: social comparison predicts a decline in the size of these coefficients between age groups, and illness preoccupation predicts an increase. The tables also present information about the statistical significance of the age trend in the coefficients: the superscript “a” denotes that age × illness interactions were statistically significant in regression models estimated using all the age groups.
TABLE 1.
Coefficients from 39 Age-Group Stratified Regressions of Self-Rated Health on Chronic Illness: Americans’ Changing Lives, 1986
| Age Group | ||||||
|---|---|---|---|---|---|---|
| 25–34 | 35–44 | 45–54 | 55–64 | 65–74 | 75+ | |
| Arthritis | 0.648 | 0.463 | 0.667 | 0.668 | 0.679 | 0.423 |
| (0.132) | (0.108) | (0.120) | (0.081) | (0.081) | (0.115) | |
| Prevalence | 8.3 | 17.6 | 29.7 | 49.7 | 58.3 | 63.0 |
| Stroke | NA | NA | NA | 1.373 | 1.081 | 0.960 |
| (0.413) | (0.323) | (0.410) | ||||
| Prevalence | 5 | 1.6 | 9 | |||
| Cancer | 2.308 | 1.100 | 1.608 | 0.526 | 0.538 | 0.648a |
| (0.468) | (0.451) | (0.377) | (0.242) | (0.208) | (0.258) | |
| Prevalence | 6 | 7 | 2.5 | 2.9 | 4.7 | 6.1 |
| Diabetes | 0.752 | 0.946 | 1.307 | 0.723 | 0.601 | 0.441a |
| (0.262) | (0.216) | (0.212) | (0.125) | (0.113) | (0.148) | |
| Prevalence | 1.5 | 3.0 | 5.7 | 9.6 | 12.6 | 14.1 |
| Heart attack | 1.259 | 1.583 | 1.262 | 1.001 | 1.096 | 0.773a |
| (0.331) | (0.240) | (0.215) | (0.124) | (0.109) | (0.143) | |
| Prevalence | 1.0 | 2.0 | 6.0 | 12.5 | 13.8 | 16.5 |
| Hypertension | 0.980 | 0.903 | 0.920 | 0.559 | 0.753 | 0.417a |
| (0.118) | (0.112) | (0.129) | (0.086) | (0.078) | (0.110) | |
| Prevalence | 7.4 | 10.4 | 19.7 | 34.5 | 44.0 | 43.3 |
| Lung disease | 0.988 | 1.663 | 1.676 | 1.010 | 0.626 | 0.747a |
| (0.261) | (0.286) | (0.272) | (0.173) | (0.161) | (0.231) | |
| Prevalence | 1.6 | 1.8 | 4.3 | 5.8 | 7.4 | 7.4 |
| N | 740 | 591 | 390 | 685 | 765 | 446 |
Note: Coefficients are from models regressing self-rated health on each chronic illness separately. All models also include controls for race/ethnicity (coefficients not shown). Coefficients are unstandardized. Standard errors are in parentheses. All coefficients significantly different from zero at p < .05.
Test of linear trend between age groups (i.e., age × illness interactions) significant at p < .05.
Table 1 suggests two related patterns, both of which point to social comparison, but not unambiguously so. For some conditions (e.g., diabetes and heart attack), the coefficients increase in size until approximately middle age (ages 45 to 54) and then decrease steadily thereafter. For other conditions (e.g., stroke and hypertension), the coefficients fall more consistently. These two patterns are distinct and do not provide absolutely clear support for social comparison. Nevertheless, for all but one of the conditions (cancer), the smallest coefficient was found for the 75 and older age group. Thus, even if illness is a preoccupation until late middle age, it is more than negated by social comparison in later life. Indeed, the decline in the coefficients is often quite large. The coefficient for cancer, for example, drops from 2.308 (for those 25 to 34) to .648 (for those age 75 and older), a decline of 72 percent. Similarly, the coefficient for heart attack falls from 1.583 (for those 35 to 44) to .773, a decline of 51 percent. The regression models explored age × illness interactions, or linear declines with age. Except for arthritis and stroke, all the declines were statistically significant.
Table 2 turns to functional limitations. Recall that as coded, functional limitations reflect four levels of consecutively more severe impairment. The results suggest that the associations between self-evaluations of general health and functional limitations increase from the age of 25 until sometime in middle age. Nevertheless, most of the coefficients decline after the age of 54. For each level of limitation, the smallest coefficient, as in Table 1, always was found for those 75 and older, and the magnitude of the decline in the coefficients was remarkable. For example, the coefficient for “most severe impairment” fell from a high of 2.379 (for those 35 to 44) to a low of 1.281 (for those 75 and older), a reduction of 46 percent. The coefficient for “least severe impairment” decreased from 1.494 (for those 25 to 34) to .422, a reduction of 72 percent. Beyond the reduction, the absolute magnitude of the coefficients is noteworthy: the coefficients for the least severe impairment were as large as or larger than the coefficients for many of the chronic conditions reported in Table 1. This suggests that individuals may judge their health more on the basis of successful role performance than on any other single factor, a result found in other studies as well (Flykesnes and Forde 1992; Liang 1986; Tessler and Mechanic 1978). Once again, tests of the significance of the declines by age were significant.
TABLE 2.
Coefficients from Six Age-Stratified Regressions of Self-Rated Health on Functional Limitations: Americans’ Changing Lives, 1986
| Age Group | ||||||
|---|---|---|---|---|---|---|
| 25–34 | 35–44 | 45–54 | 55–64 | 65–74 | 75+ | |
| Functional limitations (vs. no impairment) | ||||||
| Least severe | 1.494 | 1.197 | 1.202 | 1.004 | 0.744 | 0.422a |
| impairment | (0.247) | (0.195) | (0.215) | (0.120) | (0.099) | (0.126) |
| Moderately severe | 2.306 | 1.636 | 2.052 | 1.291 | 1.347 | 1.089a |
| impairment | (0.442) | (0.221) | (0.215) | (0.120) | (0.107) | (0.133) |
| Most severe | 2.038 | 2.379 | 1.848 | 1.606 | 1.610 | 1.281a |
| impairment | (0.314) | (0.273) | (0.275) | (0.151) | (0.140) | (0.151) |
| N | 740 | 591 | 390 | 685 | 765 | 446 |
| Functional | 1.06 | 1.11 | 1.19 | 1.45 | 1.54 | 2.02 |
| limitations mean | ||||||
Note: Coefficients are from models regressing self-rated health on dummy variables for functional limitations and race/ethnicity (coefficients for race/ethnicity not shown). Coefficients are unstandardized. Standard errors are in parentheses. All coefficients significantly different from zero at p < .05.
Test of linear trend between age groups (i.e., age × illness interactions) significant at p < .05.
Table 3 shows depressive symptoms. The standardized mean for the depression scale follows a U-shaped pattern, so that those over the age of 74 reported the most depression (for a similar pattern, see Mirowsky and Ross 1992). In marked contrast to the preceding patterns, the association between self-rated health and depressive symptoms rose with age. Indeed, the coefficient doubled in size: for those aged 25 to 34, the coefficient for depression is .236, while for those over the age of 75, the coefficient is .472. Although the largest consecutive increases were between the youngest age groups, the increases were steady between most age groups, and in contrast to the earlier results, the largest coefficient was for those aged 75 and over. In this case, a test of age trends suggests a significant increase.
Although these findings are suggestive, the interpretation is ambiguous given that (1) age-related changes may, as noted, reflect cohort-related changes instead; (2) there is a clear correlation among chronic conditions, functional impairments, and depressive symptoms, so that when all three factors are considered in the model, the relationship between depressive symptoms and self-rated health may be very different; and (3) the large association between depressive symptoms and self-rated health may reflect the unique perceptions of those nearing the end of life, rather than an aging effect per se, especially given that socioemotional selectivity focuses on how much time an individual perceives as having left to live.
Tables 4 and 5 explore these possibilities in a series of multivariate sensitivity analyses. Table 4 explores the multiplicative interactions between age and depressive symptoms, and Table 5 looks at the multiplicative interactions between age and functional limitations. Given the earlier results, the interactions should be negative in the case of functional limitations and positive in the case of depression.6 To test the sensitivity of the findings, these tables examined three things: they included independent variables that might account for the interactions; they estimated both fixed- and random-effects models; and they explored the interactions in analytically more stringent and revealing subsamples.
TABLE 5.
Random- and Fixed-Effects Regressions of Self-Rated Health on Functional Limitations × Age Interactions: Americans’ Changing Lives, 1986, 1989, 1994
| Model 1 Random Effects | Model 2 Fixed Effects | Model 3 Random Effects, Survivor Sample | |
|---|---|---|---|
| Functional limitations (vs. no impairment) | |||
| Least severe impairment | 1.413a | 0.959a | 1.331a |
| (0.153) | (0.181) | (0.160) | |
| Moderately severe impairment | 1.990a | 1.172a | 2.066a |
| (0.181) | (0.216) | (0.192) | |
| Most severe impairment | 1.895a | 1.242a | 1.807a |
| (0.181) | (0.221) | (0.194) | |
| Age | 0.012a | 0.023a | 0.011a |
| (0.001) | (0.003) | (0.001) | |
| Interactions | |||
| Least severe impairment × age | −0.012a | −0.009a | −0.011a |
| (0.002) | (0.003) | (0.002) | |
| Moderately severe | −0.014a | −0.009a | −0.017a |
| impairment × age | (0.003) | (0.003) | (0.003) |
| Most severe impairment × age | −0.011a | −0.009a | −0.011a |
| (0.003) | (0.003) | (0.003) | |
| Constant | 1.640a | 1.186a | 1.670a |
| Total N | 8,881 | 8,881 | 8,053 |
| Individuals | 3,617 | 3,617 | 3,071 |
Note: Random-effects models also include controls for race/ethnicity (coefficients not shown). Survivor sample consists of respondents who survived through all three panels of observation.
p < .01 (standard errors in parentheses).
Table 4 begins with depression, by presenting four models. The first is a simple random-effects regression model; the second is a random-effects model that includes controls for functional limitations and the number of chronic conditions; the third is a fixed-effects model; and the fourth is a random-effects model in which the sample was limited to those who survived through all three panels. These tests do little to change the conclusions drawn earlier. Indeed, the assorted models are remarkably similar. The interaction between age and depressive symptoms in Model 1 is positive and statistically significant, as we would expect. Model 2 suggests that this interaction remains significant even when controlling for functional limitations and the number of chronic conditions. Model 3 indicates that the interaction remains significant even when using fixed-effects methods. And Model 4 provides little evidence that these changes reflect the idiosyncratic perceptions of those nearing mortality in subsequent panels; indeed, the interaction in Model 4 is nearly as large as that found in Model 1.
Table 5 considers functional limitations, and the results parallel those for depressive symptoms. Model 1 confirms the declining association between functional limitations and self-rated health. Model 2 suggests that cohort effects do little to explain this decline. And Model 3 provides no evidence that the decline is driven only by those nearing death.
Given the weakening association between self-rated health and chronic conditions and the rising association between self-rated health and depressive symptoms, it is possible that in later life, self-assessments of general health reflect mental health as much as physical health. As presented in Tables 1, 3, and 4, the relative strength of the associations between self-rated health and chronic illness and between self-rated health and depressive symptoms is difficult to evaluate. The independent variables are measured using different metrics. Whereas the chronic conditions are dummy variables, the CES-D is a standardized mean. Furthermore, it is difficult to determine whether the association between depressive symptoms and self-rated health rises for all the symptoms of depression. The CES-D contains symptoms that are affective (e.g., “I felt sad”) and others that are clearly more somatic (e.g., “I could not get going”).
Table 6 provides a straightforward basis for comparison and, at the same time, explores whether the rising association is limited to a particular class of symptoms. This table presents coefficients from models regressing self-rated health on each of the 11 symptoms comprising the CES-D. The sample was limited to those 75 and older. Two coefficients are presented for each symptom, corresponding to those who experienced the symptom “some of the time” (the first column of coefficients) and those who experienced the symptom “most of the time” (the second column of coefficients). Almost all the coefficients are statistically significant and large. Indeed, the difference between those who experienced a symptom “hardly ever” and those who experienced a symptom “most of the time” is, in some cases, larger than the difference between those with and without chronic conditions. For example, the coefficients for “I felt that everything I did was an effort,” “I could not get going,” and “I felt depressed” are larger than the coefficients for any of the seven chronic conditions for those 75 and older presented in Table 1. Although the strongest associations are for symptoms involving functional limitations (e.g., “I felt that everything I did was an effort,” “I could not get going”), large associations are found for symptoms that are clearly affective. For example, the “most of the time” coefficient for “I felt depressed” is one of the largest coefficients, followed closely by the coefficient for “I felt lonely” and, when considering absolute magnitude, the coefficient for “I enjoyed life.” All three of these coefficients are larger than the coefficient for cancer. Thus, strong associations are observed for affective and somatic symptoms alike.
Conclusion
In recent years, self-rated health has assumed such prominence that researchers have done little to determine what individuals consider when they are asked to evaluate their health. My study has tried to fill several gaps. The results indicate that the meaning of self-rated health changes with age, to the point that evaluations of general health are not strictly comparable between age groups. I found two patterns in this regard. The first indicates that the correspondence between functional limitations and self-rated health declines with age, as does the correspondence between many chronic conditions and self-rated health. For all seven chronic conditions and all levels of functional limitation, the association with self-rated health was weakest among those 75 and older. The second pattern indicates that the correspondence between depressive symptoms and self-rated health increases precipitously with age. This second pattern is as striking for its strength as it is for its pattern. Indeed, after the age of 74, some depressive symptoms become more strongly associated with self-rated health than several of the chronic—and generally severe—conditions. For example, agreement with the statement “I feel depressed most of the time” was more strongly associated with self-rated health than were any of the seven chronic conditions, with the exception of stroke. Similarly, agreement with the statement “I enjoy life most of the time” was more closely associated with self-rated health than cancer was. Although functional limitations maintained the strongest association, depressive symptoms eventually became a close rival.
In documenting the increasing salience of depressive symptoms, the results diverged from previous research in several respects and call for several reconsiderations. Most notably, the results call for reconsidering the overwhelming importance of maintaining a positive sense of health and, relatedly, the “biases” thought to motivate social comparison. To be sure, social comparison accurately anticipates the declining significance of both chronic illness and functional limitations, and in this regard, self-assessments of general health may appear more optimistic than do assessments based on the presence or absence of disease or impairment. But social comparison does not accurately anticipate the growing significance of depressive symptoms, given that its guiding principle is that individuals tend to inflate their sense of health beyond what their “objective” health might allow. If self-evaluations of general health reflected a defensive reaction to increasingly poor health, we would not expect the importance of depression to increase, especially given that depressive symptoms are common among those over the age of 74. What these results imply instead is that the elderly change their evaluations in ways that reflect their changing values. As socioemotional selectivity anticipates, the results suggest that emotions are an increasingly salient dimension of health, to the point of outweighing other, more conventional features of morbidity.
Although the results point to the growing importance of depressive symptoms, they should be read cautiously with respect to what they reveal about beliefs about depression. Indeed, there has been much discussion of the reasons for the elderly's lack of treatment for depression, and much of this research has emphasized patient-level barriers, including but not limited to stigma (Unützer et al. 1999). Even though depressive symptoms may be increasingly pertinent to self-evaluations of general health, this does not mean that the elderly are any more supportive of psychiatric treatment. The results encourage more complex and fine-grained explorations of the elderly's beliefs, with a number of intriguing possibilities. For example, in contrast to younger generations, older generations may be more inclined to view depression as an important feature of health but less inclined to articulate and present their symptoms in ways that lead to treatment. Age groups may differ just as much in their beliefs about the appropriate treatment for depression as in how important avoiding depression is for maintaining one's quality of life.
The results also speak to the “validity” of self-rated health. Researchers continue to be drawn to self-rated health because of its remarkable ability to predict mortality. In this regard, the results do not indicate that self-rated health is any less valid because it is associated more closely with depression. The association between chronic illness and self-rated health is not eliminated entirely; the age-based declines should be understood as declines relative to former levels and not as declines to the point of statistical or substantive insignificance. Furthermore, depression itself is not entirely unrelated to mortality. Several studies have demonstrated a relationship between depressive symptoms and accelerated mortality (Anda et al. 1993; Cohen and Rodriguez 1995; Frasure-Smith, Lesperance, and Talajic 1995; Glassman and Shapiro 1998; Kiecolt-Glaser et al. 2002). Although the reasons for this relationship are not well understood and there is some skepticism regarding whether the relationship is causal, the relationship does imply that self-rated health's ability to predict mortality may not be compromised simply because self-rated health is associated more closely with depressive symptoms and less so with chronic conditions.
Perhaps more troubling are the results’ implications for research concerned with age trajectories in health. Social epidemiology and demography have long been concerned with the shape of health disparities across the life course. A key debate has been whether the effects of socioeconomic status increase with age (consistent with a cumulative advantage approach) or whether they increase until late middle age and decrease steadily thereafter (consistent with an age-as-leveler approach) (Ross and Wu 1996). Empirical tests of these alternative perspectives have yielded mixed results, with some finding evidence for age-as-leveler (House et al. 1994) and others for cumulative advantage (Lynch 2003). If the results presented here reflect broader patterns, researchers relying on self-rated health as their sole outcome should be cautious about inferring changes in the effects of socioeconomic status on morbidity as a whole when such changes might instead reflect changes in what self-rated health is capturing. Finer-grained patterns are possible, including that the association between socioeconomic status and mental health strengthens while the association between socioeconomic status and physical health weakens. Disentangling these possibilities will require considering a variety of outcomes, including both physical and mental health, and paying particular attention to the ways in which these different outcomes diverge.
This study has several important limitations. First, although the data are longitudinal and cover nearly a decade, there undoubtedly have been important changes since 1994. The availability of even more pharmaceuticals, combined with the continued growth of direct-to-consumer marketing, may have significantly altered public perceptions of health and well-being (see Conrad 2005). Although changes between periods are not necessarily related to changes between age groups, future research should be attentive to the speed with which perceptions of health can progress and elevate the perceived severity of once minor conditions. Second, while the ACL is nationally representative and oversamples the elderly, it almost certainly underrepresents the severely ill, given that it samples households. Those coping with an illness severe enough to require institutionalization may have views that are very different from those who are well enough to live at home. That said, there is little to suggest that a more thoroughly representative sample would yield radically different results. As shown earlier, the results are remarkably robust to several forms of selective sample attrition. Third, the results may be very different among cultures. Indeed, the psychological processes underlying the salience of depressive symptoms may be uniquely Western, especially if they are rooted in the elderly's search for emotional satisfaction (Markus and Kitayama 1991). Fourth, while the ACL contains a wide variety of particular health indicators, other elements of health could not be explored. More objective clinical indicators—as uncovered, for example, in blood tests or a physical exam—may have a very different relationship to self-rated health than do the self-reported indicators considered here.
This study encourages additional research on the disjuncture between particular illnesses and self-evaluations of general health. Although researchers regularly speculate about group differences in beliefs about health and illness, they have done surprisingly little empirical research on such differences. This study's methods can easily be generalized to examine other sociodemographic factors, including education and race/ethnicity. More generally, the results encourage additional research on the subjectivity, construal, and social psychology of health. Although self-evaluations of general health overlap with clinical outcomes, the disjuncture between the two provides important clues to how different groups evaluate health, as well as insights into the particular health care needs of different populations.
Finally, this study encourages additional emphasis on depression as a feature of health, especially among the elderly. Depression is not conventionally considered to be an indicator of morbidity. Furthermore, it is likely to be overlooked when treating the elderly (Unützer et al. 1999). Some researchers suggest that the pursuit of happiness may only be a concern among recent cohorts, who are no longer concerned with basic survival (Felton 1987). However, depression's standing—at least in the health literature—appears be changing. Some researchers have pushed for recognizing depression as a disease equivalent to other somatic conditions in its severity and impact (e.g., see Kramer 2005). Furthermore, researchers now recognize that depression contributes enormously to the total amount of disability experienced in a lifetime (see Murray and Lopez 1996). The results of the present study are consistent with the spirit of this literature in suggesting that depression is an important feature of health and, indeed, that it might be a key feature of health in the mind of America's elderly population.
Acknowledgments
This research was funded by NIH-NIA grant AG-12836. The author thanks Paul Allison, Thomas Croghan, Bernice Pescosolido, Herb Smith, and Beth Soldo for helpful comments and discussions, as well as participants at the RAND Sociology and Demography seminar. The collectors of Americans’ Changing Lives are not responsible for the results and interpretations presented in this article.
Endnotes
There are important exceptions to this finding. Among the most important is that individuals may compare themselves with those who are worse off but continue to affiliate with those who are better off (Taylor and Lobel 1989).
Because of the unequal probability of selection, all descriptive statistics (e.g., prevalence estimates) were weighted. The regression models, however, were not. Because the models include or are stratified by the features of sample selection (i.e., age and race/ethnicity), the coefficients are unbiased and consistent even without the use of weights (Winship and Radbill 1994).
There are several versions of self-rated health. Some include only four response categories, and others are explicitly asked in relative terms. Yet despite their differences, these versions correlate very highly with one another, and their empirical properties (e.g., the ability to predict mortality) are nearly identical (Idler and Benyamini 1997).
All the analyses use linear regression and assume that adjacent categories are equidistant. Supplementary analyses relaxed this assumption. Two general types of models were explored. First, ordered-logistic regression models were estimated (Long 1997). Such models estimate a series of cut-points corresponding to the distance between categories. Second, self-rated health was recoded to allow, as suggested in previous research, the distance between categories of good health to be smaller than that between categories of poor health: I estimated models using self-rated health squared as an outcome, as well as models that recoded self-rated health as 5, 10, 20, 70, 85, rather than 1, 2, 3, 4, 5 (see Diehr et al. 2001). In all these cases, the results were comparable to those presented later: all significant age × illness interactions that are reported as significant also were significant using these alternative techniques. Although perhaps at odds with the intuition that excellent and very good health are distinct from the remaining categories, this result is consistent with methodological research suggesting that self-rated health behaves like a continuous variable (Manderback, Lahelma, and Martikainen 1998; Manor, Matthews, and Power 2000).
The language of “fixed” effects refers to “fixed” individual-specific parameters. It does not refer to “fixed” coefficients, as in multilevel modeling. In that context, a coefficient can either be “fixed” to be constant within higher-level units or “random” and allowed to vary.
Because the pattern is not entirely linear (as documented earlier), these interactions provide a conservative test of age-related change. A more robust test—if also more complex—would include interactions with age and age-squared.
References
- Afflect G, Tennen H, Pfeiffer C, Fifield J. Social Comparisons in Rheumatoid Arthritis: Accuracy and Adaptational Significance. Journal of Social and Clinical Psychology. 1988;6:219–34. [Google Scholar]
- Allison PD. Change Scores as Dependent Variables in Regression Analysis. In: Clogg Clifford C., editor. Sociological Methodology. Oxford: Blackwell; 1990. pp. 93–114. [Google Scholar]
- Anda R, Williamson D, Jones D, Macera C, Eaker E, Glassman A, Marks J. Depressed Affect, Hopelessness, and the Risk of Ischemic Heart Disease in a Cohort of U.S. Adults. Epidemiology. 1993;4:285–94. doi: 10.1097/00001648-199307000-00003. [DOI] [PubMed] [Google Scholar]
- Baltagi BH. Econometric Analysis of Panel Data. New York: Wiley; 1995. [Google Scholar]
- Blanchard-Fields F. Reasoning on Social Dilemmas Varying in Emotional Saliency: An Adult Developmental Perspective. Psychology and Aging. 1986;1:325–33. doi: 10.1037//0882-7974.1.4.325. [DOI] [PubMed] [Google Scholar]
- Blanchard-Fields F, Jahnke HC, Camp C. Age Differences in Problem-Solving Style: The Role of Emotional Salience. Psychology and Aging. 1995;10:173–80. doi: 10.1037//0882-7974.10.2.173. [DOI] [PubMed] [Google Scholar]
- Borawski EA, Kinney JM, Kahana E. The Meaning of Older Adults’ Health Appraisals: Congruence with Health Status and Determinant of Mortality. Journal of Gerontology: Social Science. 1996;51B:S157–70. doi: 10.1093/geronb/51b.3.s157. [DOI] [PubMed] [Google Scholar]
- Carstensen LL, Isaacowitz DM, Charles ST. Taking Time Seriously: A Theory of Socioemotional Selectivity. American Psychologist. 1999;54:165–81. doi: 10.1037//0003-066x.54.3.165. [DOI] [PubMed] [Google Scholar]
- Case A, Paxson C. Sex Differences in Morbidity and Mortality. Demography. 2005;42:189–214. doi: 10.1353/dem.2005.0011. [DOI] [PubMed] [Google Scholar]
- Cleary PD, Edgman-Levitan S. Health Care Quality: Incorporating Consumer Perspectives. Journal of the American Medical Association. 1997;278:1608–12. [PubMed] [Google Scholar]
- Cohen S, Rodriguez MS. Pathways Linking Affective Disturbances and Physical Disorders. Health Psychology. 1995;14:374–80. doi: 10.1037//0278-6133.14.5.374. [DOI] [PubMed] [Google Scholar]
- Conrad P. The Shifting Engines of Medicalization. Journal of Health and Social Behavior. 2005;46:3–14. doi: 10.1177/002214650504600102. [DOI] [PubMed] [Google Scholar]
- Cronbach LJ. Coefficient Alpha and the Internal Structure of Tests. Psychometrika. 1951;16:297–334. [Google Scholar]
- Croyle RT. Appraisal of Health Threats: Cognition, Motivation, and Social Comparison. Cognitive Therapy and Research. 1992;16:165–82. [Google Scholar]
- DeVellis RF, Holt K, Renner BR, Blalock SJ, Blanchard LW, Cook HL, Klotz ML, Mikow V, Harring K. The Relation of Social Comparison to Rheumatoid Arthritis Symptoms and Affect. Basic and Applied Social Psychology. 1990;11:1–18. [Google Scholar]
- Diehr P, Patrick DL, Spertus J, Kiefe CI, McDonell M, Fihn SD. Transforming Self-Rated Health and the SF-36 Scales to Include Death and Improve Interpretability. Medical Care. 2001;39:670–80. doi: 10.1097/00005650-200107000-00004. [DOI] [PubMed] [Google Scholar]
- England P, Farkas G, Kilbourne BS, Dou T. Explaining Occupational Sex Segregation and Wages: Findings from a Model with Fixed Effects. American Sociological Review. 1988;53:544–58. [Google Scholar]
- Felton BJ. Cohort Variations in Happiness: Some Hypotheses and Exploratory Analyses. International Journal of Aging and Human Development. 1987;25:27–42. doi: 10.2190/5LC0-LFA2-30VW-UGBV. [DOI] [PubMed] [Google Scholar]
- Ferraro KF, Farmer MM. Utility of Health Data from Social Surveys: Is There a Gold Standard for Measuring Morbidity? American Sociological Review. 1999;64:303–15. [Google Scholar]
- Flykesnes K, Forde OH. The Tromso Study: Predictors of Self-Evaluated Health—Has Society Adopted the Expanded Health Concept? Social Science and Medicine. 1991;32:141–6. doi: 10.1016/0277-9536(91)90053-f. [DOI] [PubMed] [Google Scholar]
- Flykesnes K, Forde OH. Determinants and Dimensions Involved in Self-Evaluations of Health. Social Science and Medicine. 1992;35:271–9. doi: 10.1016/0277-9536(92)90023-j. [DOI] [PubMed] [Google Scholar]
- Frasure-Smith N, Lesperance F, Talajic M. The Impact of Negative Emotions on Prognosis Following Myocardial Infarction: Is It More Than Depression? Health Psychology. 1995;14:388–98. doi: 10.1037//0278-6133.14.5.388. [DOI] [PubMed] [Google Scholar]
- Glasser M, Gravdal JA. Assessment and Treatment of Geriatric Depression in Primary Care Setting. Archives of Family Medicine. 1997;6:433–8. doi: 10.1001/archfami.6.5.433. [DOI] [PubMed] [Google Scholar]
- Glassman AH, Shapiro PA. Depression and the Course of Coronary Artery Disease. American Journal of Psychiatry. 1998;155:4–11. doi: 10.1176/ajp.155.1.4. [DOI] [PubMed] [Google Scholar]
- Goldstein MS, Siegel JM, Boyer R. Predicting Changes in Perceived Health Status. American Journal of Public Health. 1984;74:611–4. doi: 10.2105/ajph.74.6.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guttman L. The Basis for Scalogram Analysis. In: Stouffer S A, editor. Measurement and Prediction: Studies in Social Psychology in World War II. Vol. 4. Princeton, N.J.: Princeton University Press; 1950. pp. 60–90. [Google Scholar]
- Harlow SD, Linet MS. Agreement between Questionnaire Data and Medical Records: The Evidence for Accuracy of Recall. American Journal of Epidemiology. 1989;129:233–48. doi: 10.1093/oxfordjournals.aje.a115129. [DOI] [PubMed] [Google Scholar]
- Helgeson VS, Taylor SE. Social Comparisons and Adjustment among Cardiac Patients. Journal of Applied Social Psychology. 1993;23:1171–95. [Google Scholar]
- Hoeymans N, Feskens EJ, Kromhout D, van den Bos GA. Ageing and the Relationship between Functional Status and Self-Rated Health in Elderly Men. Social Science and Medicine. 1997;45:1527–36. doi: 10.1016/s0277-9536(97)00089-0. [DOI] [PubMed] [Google Scholar]
- House JS. Ann Arbor, Ann Arbor: University of Michigan, Institute for Social Research, Survey Research Center, Inter-University Consortium for Political and Social Research; 2003. Americans’ Changing Lives: I, II, and III, 1968, 1989, and 1994 (computer file) ICPSR version. (producer), 2002. distributor. [Google Scholar]
- House JS, Lepkowski JM, Kinney AM, Mero RP, Kessler RC, Herzog AR. The Social Stratification of Aging and Health. Journal of Health and Social Behavior. 1994;35:213–34. [PubMed] [Google Scholar]
- Idler EL. Age Differences in Self-Assessments of Health: Age Changes, Cohort Differences, or Survivorship? Journal of Gerontology: Social Sciences. 1993;48:S289–300. doi: 10.1093/geronj/48.6.s289. [DOI] [PubMed] [Google Scholar]
- Idler EL, Benyamini Y. Self-Rated Health and Mortality: A Review of Twenty-seven Community Studies. Journal of Health and Social Behavior. 1997;38:21–37. [PubMed] [Google Scholar]
- Idler EL, Hudson SV, Leventhal H. The Meanings of Self-Ratings of Health: A Qualitative and Quantitative Approach. Research on Aging. 1999;21:458–76. [Google Scholar]
- Johnson RJ, Wolinsky FD. The Structure of Health Status among Older Adults: Disease, Disability, Functional Limitation, and Perceived Health. Journal of Health and Social Behavior. 1993;34:105–21. [PubMed] [Google Scholar]
- Jylhä M, Guralnik JM, Balfour J, Fried LP. Walking Difficulty, Walking Speed, and Age as Predictors of Self-Rated Health: The Women's Health and Aging Study. Journals of Gerontology Series A: Biological Sciences & Medical Sciences. 2001;56:M609–17. doi: 10.1093/gerona/56.10.m609. [DOI] [PubMed] [Google Scholar]
- Kaplan GA, Camacho T. Perceived Health and Mortality: A Nine-Year Follow-up of the Human Population Laboratory Cohort. American Journal of Epidemiology. 1983;117:292–304. doi: 10.1093/oxfordjournals.aje.a113541. [DOI] [PubMed] [Google Scholar]
- Kiecolt-Glaser JK, McGuire L, Robles TF, Glaser R. Emotions, Morbidity, and Mortality: New Perspectives from Psychoneuroimmunology. Annual Review of Psychology. 2002;53:83–107. doi: 10.1146/annurev.psych.53.100901.135217. [DOI] [PubMed] [Google Scholar]
- Kramer PD. Against Depression. New York: Viking; 2005. [Google Scholar]
- Krause NM, Jay GM. What Do Global Self-Rated Health Items Measure? Medical Care. 1994;32:930–42. doi: 10.1097/00005650-199409000-00004. [DOI] [PubMed] [Google Scholar]
- Leventhal EA. Aging and the Perception of Illness. Research on Aging. 1984;6:119–25. doi: 10.1177/0164027584006001007. [DOI] [PubMed] [Google Scholar]
- Leventhal EA, Leventhal H, Schaefer P, Easterling D. Conservation of Energy, Uncertainty Reduction, and Swift Utilization of Medical Care among the Elderly. Journal of Gerontology. 1993;48:78–86. doi: 10.1093/geronj/48.2.p78. [DOI] [PubMed] [Google Scholar]
- Levkoff SE, Cleary PD, Wetle T. Differences in the Appraisal of Health between Aged and Middle-Aged Adults. Journal of Gerontology. 1987;42:114–20. doi: 10.1093/geronj/42.1.114. [DOI] [PubMed] [Google Scholar]
- Liang J. Self-Reported Physical Health among Aged Adults. Journal of Gerontology. 1986;41:248–60. doi: 10.1093/geronj/41.2.248. [DOI] [PubMed] [Google Scholar]
- Long JS. Regression Models for Categorical and Limited Dependent Variables. Thousand Oaks, Calif.: Sage; 1997. [Google Scholar]
- Lynch SM. Cohort and Life-Course Patterns in the Relationship between Education and Health: A Hierarchical Approach. Demography. 2003;40:309–31. doi: 10.1353/dem.2003.0016. [DOI] [PubMed] [Google Scholar]
- Maddox GL, Douglass EB. Self-Assessment of Health: A Longitudinal Study of Elderly Subjects. Journal of Health and Social Behavior. 1973;14:87–93. [PubMed] [Google Scholar]
- Manderback K, Lahelma E, Martikainen P. Examining the Continuity of Self-Rated Health. International Journal of Epidemiology. 1998;27:208–13. doi: 10.1093/ije/27.2.208. [DOI] [PubMed] [Google Scholar]
- Manor O, Matthews S, Power C. Dichotomous or Categorical Response? Analyzing Self-Rated Health and Lifetime Social Class. International Journal of Epidemiology. 2000;29:149–57. doi: 10.1093/ije/29.1.149. [DOI] [PubMed] [Google Scholar]
- Markus HR, Kitayama S. Culture and Self: Implications for Cognition, Emotion, and Motivation. Psychological Review. 1991;98:224–53. [Google Scholar]
- Mechanic D, Angel RJ. Some Factors Associated with the Report and Evaluation of Back Pain. Journal of Health and Social Behavior. 1987;28:131–9. [PubMed] [Google Scholar]
- Mirowsky J, Ross CE. Age and Depression. Journal of Health and Social Behavior. 1992;33:187–205. [PubMed] [Google Scholar]
- Murray CJL, Lopez AD. The Global Burden of Disease: A Comprehensive Assessment of Mortality and Disability from Disease, Injuries, and Risk Factors in 1990 and Projected to 2020. Cambridge, Mass.: Harvard School of Public Health for the World Health Organization; 1996. [Google Scholar]
- Patrick DL, Erickson P. Health Status and Health Policy: Quality of Life in Health Care Evaluations and Resource Allocation. New York: Oxford University Press; 1993. [Google Scholar]
- Pijls LT, Feskens EJM, Kromhout D. Self-Rated Health, Mortality, and Chronic Disease in Elderly Men: The Zutphen Study, 1985–1990. American Journal of Epidemiology. 1993;138:840–48. doi: 10.1093/oxfordjournals.aje.a116787. [DOI] [PubMed] [Google Scholar]
- Radloff L. The CES-D Scale: A Self Report Depression Scale for Research in the General Population. Applied Psychological Measurement. 1977;1:385–401. [Google Scholar]
- Rakowski W, Cryan CD. Associations among Health Perceptions and Health Status within Three Age Groups. Journal of Aging and Health. 1990;2:58–80. [Google Scholar]
- Rosenberg CE. The Tyranny of Diagnosis: Specific Entities and Individual Experience. Milbank Quarterly. 2002;80:237–60. doi: 10.1111/1468-0009.t01-1-00003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosenstock IM. Why People Use Health Services. Milbank Quarterly. 1966;44:94–106. [PubMed] [Google Scholar]
- Ross CE, Wu C-L. Education, Age, and the Cumulative Advantage in Health. Journal of Health and Social Behavior. 1996;37:104–20. [PubMed] [Google Scholar]
- Ruo B, Rumsfeld JS, Hlatky MA, Liu H, Browner WS, Whooley MA. Depressive Symptoms and Health-Related Quality of Life. Journal of the American Medical Association. 2003;290:215–21. doi: 10.1001/jama.290.2.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ryder NB. The Cohort as a Concept in the Study of Social Change. American Sociological Review. 1965;30:843–61. [PubMed] [Google Scholar]
- Spiers N, Jagger C, Clarke M. Physical Function and Perceived Health: Cohort Differences and Interrelationships in Older People. Journal of Gerontology: Social Sciences. 1996;51B:S226–33. doi: 10.1093/geronb/51b.5.s226. [DOI] [PubMed] [Google Scholar]
- Starr P. The Social Transformation of American Medicine. New York: Basic Books; 1982. [Google Scholar]
- Strain LA. Good Health: What Does It Mean in Later Life? Journal of Aging and Health. 1993;5:338–64. [Google Scholar]
- Suls J, Marco CA, Tobin S. The Role of Temporal Comparison, Social Comparison, and Direct Appraisal in the Elderly's Self-Evaluations of Health. Journal of Applied Social Psychology. 1991;21:1125–44. [Google Scholar]
- Taylor SE, Lobel M. Social Comparison Activity under Threat: Downward Evaluation and Upward Contacts. Psychological Review. 1989;96:569–75. doi: 10.1037/0033-295x.96.4.569. [DOI] [PubMed] [Google Scholar]
- Tessler RC, Mechanic D. Psychological Distress and Perceived Health Status. Journal of Health and Social Behavior. 1978;19:254–62. [PubMed] [Google Scholar]
- Tornstam L. Health and Self-Perception: A System's Theoretical Approach. The Gerontologist. 1975;27:264–70. doi: 10.1093/geront/15.3.264. [DOI] [PubMed] [Google Scholar]
- Unützer J, Katon W, Sullivan M, Miranda J. Treating Depressed Older Adults in Primary Care: Narrowing the Gap between Efficacy and Effectiveness. Milbank Quarterly. 1999;77:225–56. doi: 10.1111/1468-0009.00132. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilson IB, Cleary PD. Linking Clinical Variables with Health-Related Quality of Life. Journal of the American Medical Association. 1995;273:59–65. [PubMed] [Google Scholar]
- Winship C, Radbill L. Sampling Weights and Regression Analysis. Sociological Methods and Research. 1994;23:230–57. [Google Scholar]
- Wood JV, Taylor SE, Lichtman RR. Social Comparison in Adjustment to Breast Cancer. Journal of Personality and Social Psychology. 1985;49:1169–83. doi: 10.1037//0022-3514.49.5.1169. [DOI] [PubMed] [Google Scholar]
