|
|
||||||||
POLICY, BIOLOGY, AND HEALTH |
Walter M. Bortz. MD, is with the Stanford University School of Medicine, Portola Valley, Calif.
Correspondence: Requests for reprints should be sent to Walter M. Bortz, MD, Stanford University School of Medicine, 167 Bolivar Lane, Portola Valley, CA, 94028 (e-mail: drwbortz{at}aol.com).
| ABSTRACT |
|---|
|
|
|---|
Clinical medicine and health policy planning find common cause as they seek to define the determinants of health. There is substantial recent interest in the social ecology in which health is embedded. However, biology is where these contributing environmental factors are translated.
I provide a new conceptual framework for the biological determinants of health. The old public health rubric of host, agent, and environment as the features that define the root elements of health is an impoverished scheme, because it does not represent our new appreciation of genetic and aging contributions to phenotypic health. I propose genes, external agency, internal agency, and aging as more operationally helpful determinants that effectively describe the biological experience of the organism.
This scheme has the advantage of differentiating those agencies that are practically approachable, and therefore deserving of increased attention and investment, and those that are currently intractable.
| ZIMMERMANS LAW STATES |
|---|
|
|
|---|
Aligned with this economic reality is the fact that medical science has devoted almost the entirety of its intellectual and financial capital to the elucidation of disease mechanisms and their relief. The pathogenesis of most illness is now known in great detail, yet the causative features that underlie health remain largely unexplored.
It is commonly acknowledged that the root causes of both disease and health involve multiple agencies. The hierarchical nature of multiple causes, "causes of causes," recognizes that some causes are more proximate or immediate than others.2 The death certificate form in California requests the following information: (1) immediate cause of death, (2) secondary cause of death, and (3) other contributing conditions. McGinnis and Foege examined this "cause of cause" idea in their article "Actual Causes of Death in the United States."3 McGinnis and Foege contrasted the traditional list of causes of death with actual causes, most of which were behavioral and lifestyle in origin.
The summary figure of the determinants of health provided in Healthy People 2010 displays multiple contributing agencies within an interactive matrix formulation (Figure 1
).4(p18, Figure 7) However, within the formulation, it is evident that the biological factors are more proximate determinants than the socioeconomic contributors, which are upstream and ultimate in their role. Nearly the entirety of the MarchApril 2002 issue of Health Affairs was devoted to the determinants of health and emphasized the social ecology in which health is enmeshed. Deaton lamented the ignorance of the biological determinants that are not revealed by clinical measurements and that are obscured by the long time interval between cause and outcome.2 However, it is from biological factors that the functional well-being of the organism basically derives as the final common pathway to health. I explore these biological determinants of health and provide a new simple conceptual framework for their consideration. I hope that such a proposition assists in strategic planning that differentiates those determinants that are tractable and those that currently lie outside clinical approach.4
|
| DETERMINANTS OF HEALTH |
|---|
|
|
|---|
I propose that these 4 factors account, occurring in innumerable combinations and chronologies, for the totality of the human health experience, both individual and collective. Hypothetically, if the first 3 of these 4 factors could be eliminated through a perfect design or gene set, no accidents or external disruptions, and ideal maintenance or balanced internal dynamics, then the car or body would have the opportunity to die of "natural causes"aging, which rarely if ever occurs with either.
Genes
The 30 000-gene human genome was widely touted as the ultimate determinant of well-being and illness. This conjecture has now largely been displaced by the recognition that genes actually represent only restricted arbiters of health whose repertoire depends on differential cueing.5
Quantitatively, Strohman estimated that less than 2% of human illness is attributable to a faulty single gene locus.6 Virtually all diseases exhibit mosaic patterns with genetic complexity. An approach widely used to quantify genetic contribution is to investigate the health history of identical twins. If genes were ultimately determinative, and the other 3 agencies were only negligible factors, identical twins would die simultaneously of the same disease. This situation is far from the case. Common neurological diseases of older persons have been shown to have low concordance among twins.7,8 Further, studies of monozygotic and dizygotic twins indicate that heredity accounts for 15% to 20% of the differences in human longevity.9 Genes matter; however, their real significance lies not in their essence, but in their interrelations with the other components of health.10
External Agency as a Health Determinant
Throughout recent history, the major threat to human health has been the byproduct of an adverse encounter with a hostile threat. Pasteur demonstrated that the previously held attribution of sickness to metaphysical punishment motifs was wrong and that a microbe was more properly labeled as the devil.11 The appropriate recourse to this new reality was to construct a therapeutic armor to shield the unsuspecting host from his or her dangerous environment. The varieties of health threat that the external world presents are immense in scope and timing. Injury, infection, and malignancy each are huge demerits. These threats may diminish the health reserve catastrophically or may conspire through the accumulation of trivial or sequential insults. For the most part, they are acute in their representation and are usually confined to a defect in one of the bodys component parts.
In my opinion, the conditions involved in external agency are responsible for the development of the majority of the current medical enterprise of hospitals, surgery, technology, and pharmacy. Medical science has gaudy credentials gained by confronting the conditions secondary to faulty external agency. Technical advance has allowed address and redress of countless illness states that were unapproachable just a few decades ago. In addition, the issue of prevention is presented when considering external agency as a health determinant. Most infection, injury, and malignancy is preventableand preventing them is a strategy far preferable to curing them (cheaper, too). To paraphrase Oliver Wendell Holmes, "The shield is nobler than the spear."12
Internal Agency as a Health Determinant
The era of the dominance of external agents as prime determinants of health has been replaced by the reality of disordered internal function as the principal causes of the chronic illness patterns prevalent today. Conditions caused by faulty internal agency do not feature a dominant external perturbation. These conditions tend to involve the entire system rather than components as in external agency problems. Instead of the environment being a threat to well-being, internal agency connotes an appropriate and constant interplay of the host and environment. The environment becomes the source of organic order, stability, and, therefore, health. This new conceptualization is captured by the term homeodynamics, as specified by Yates.13
Homeodynamics is a substantially more effective term than homeostasis, helpfully supplied by Cannon more than 80 years ago.14 Homeostasis addresses the reality of our internally stabilizing processes, but the connotation of stasis is alien to living processes. Yatess proposition defines how environmental energetic stimuli are inscribed onto the organism through myriad transduction processes. The extraordinary plasticity of all parts of our body is a vivid demonstration of how form follows function and how the body is constantly remodeling in response to the energetic field in which it is immersed. We become what we do through homeodynamic reshaping at every level.
Environmental interfacing with a healthy body has 2 primary expressions: fuel and energy. The role of adequate nutrition in health maintenance has been voluminously documented. Excesses and deficiencies exact certain tolls. Less well displayed is the health risk posed by inappropriate energetic stimulation. This maladaptation becomes increasingly important as age proceeds. This misapplied energy comes in 2 forms: too much and too little. Too much energetic interfacing is known by the term stress; too little is known as disuse. Both have vast negative consequences on the afflicted organism, and both are inadequately recognized as basic health threats. Part of the reason for their lack of proximal recognition, diagnosis, and treatment is the long timeline from cause to effect.
Selye first elaborated the diverse spectrum of stressors with which organisms are assaulted. He labeled the host response to these challenges the "general adaptation syndrome."15 McEwen coined the term "allostatic load" to quantitate the cumulative physiological toll exerted on a body over time by efforts to adapt to life experience.16 A 1997 report by Seeman et al. indicated that allostatic load was a better predictor of cognitive decline and cardiovascular performance in older persons than more standard parameters.17
The converse of stress is disuse; disuse means too little energetic interchange, usually manifested through a sedentary lifestyle. I codified the common clinical parameters within the rubric of the "disuse syndrome"18: cardiovascular vulnerability, musculoskeletal fragility, immunologic susceptibility, metabolic instability, depression, and precocious aging. Each of these diverse components has discrete, deterministic mechanisms that relate insufficient energetic throughput to the frequently observed disease byproduct. They are not genetic or externally produced, nor are they secondary to aging per se; instead, they are the byproducts of protracted disuse.
The most vivid demonstration of disuse occurs in muscle. With continued use, muscle strength and power deteriorates at a slow rate, but with disuse, as in space travel or a casted limb, muscle strength can decay at 1% per day.19 Every organ, tissue, and function is beholden to this appropriate homeodynamic linkage. The energy transduction and gene expression details inherent in this remodeling are now known in great detail.
"VO2 max" is a congregate, physiological parameter that collectively reflects how an organism extracts oxygen from the atmosphere and conducts it through the respiratory and circulatory systems to every cell, where it is used to provide the spark that fuels metabolism and runs life. A physically fit person exhibits a decline in VO2 max at the rate of 0.5% per year. An unfit person, conversely, loses this basic competence at the rate of 2% per year4 times as fast. This is not the result of bad genes or extrinsic agency or aging; it is the result of faulty internal agency.20 Both muscle strength and VO2 max have been shown to be powerful, predictive biomarkers for subsequent disability and death.21,22
In my opinion, this categorydefective internal agencyis the predominant determinant of failing health in older people, particularly because chronic, time-sensitive illnesses are our most common demons. Unfortunately, the competence of the medical enterprise and its curing mission finds only limited success with the conditions attributable to defective internal agency. Heart disease, arthritis, type II diabetes, and strokes are palliated at great cost, but they are not cured. However, they are preventable through redress of energetic imbalance and nutritional excess.
Aging
The participation of the process of aging in the human condition has long been the province of playwrights, theologians, and charlatans. Only recently has aging been held to rigorous analysis. No longer is it considered a disease susceptible to a curing potion, gland, or surgery. Instead, it is seen as a lifelong development and undevelopment process that lends itself to a thermodynamic analysis within Yates formulation of homeodynamics.13 Aging is the result of entropic decay inherent in metabolic process, which is partially but incompletely offset by countering mechanisms. Aging is wear and tear minus repair.
In the past 10 years, 2 reports provided a vital, quantitative measure of the basic rate of aging.23,24 The decline in function in 12 organ systems has an underlying rate of 0.5% per year in all systems, from ages 30 through 70, where most data are available. This figure is thought, therefore, to represent the underlying rate at which health reserves are debited, specifically, because of chronological, entropic age process. The 0.5% per year rate of decline also describes the age rate of decline in several athletic performances.23 Previously noted were observed rates ranging from 2% per year to 1% per week. Such declines are commonly ascribed to aging. However, these declines are caused not by aging but by more tractable agencies.
| DISCUSSION |
|---|
|
|
|---|
Diamond surveyed a series of "biological safety factors" in a variety of species from squid to primates and found a range of 1.3 to 10 total functional to basal capacity.25 In humans, the reserve margin of health is most easily observed in the case of the paired organs in which a total loss of 1 organ leads to little apparent loss in function. Many other capacitiescardiac reserve, oxygen transport, neurotransmitter levels, muscle power, arterial cross-section, creatinine clearance, liver mass, sensory and cognitive capacitiesexhibit similar safety margins. A common, but not universal, implication is that not until 70% of maximal capacity is lost does symptomatic impairment of health appear.26 Verdery termed the zone of 20% to 40% of maximal function "the disability to survival span."27 The World Health Organization proposed that health represents that state before impaired health becomes apparent.28 Clearly the lack of awareness of symptomatic loss involves a substantial physiological reserve (Figure 2
). This concept suggests that health exists above the symptomatic threshold value of 30% of optimal/maximal function. Below 30% of maximum, there is only a small margin of safety before profound threat to function and survival occurs. I propose that it is in this 20% to 30% range where most medical encounters occur, and most expenses are generated.
|
The range of 20% to 30% of maximum capacity represents the frailty zone of precariously limited vital reserve. A person can lose 70% of his or her full function catastrophically as a result of external events, or the loss may occur more slowly from accumulated minor decrements caused by internal agency or to aging. In the real world, health is determined by a summation of the effects of 4 listed agencies. What is crucial to observe, however, is that only those determinants caused by faulty external and internal agency are susceptible to clinical intervention. Genetic aberration and the process of aging, which, although theoretically approachable, are still remote in their practicability.
Redress of disordered external and internal agencies, which quantitatively are the major biological determinants of health, is eminently practicable, and attention to the behavioral causes of these causes appears acutely necessary. Such active pursuit is the most likely strategy to succeed in fulfilling the goals of Healthy People 2010.4
| Footnotes |
|---|
Accepted for publication March 12, 2004.
| References |
|---|
|
|
|---|
2. Deaton A. Policy implications of the gradient of health and wealth. Health Aff.2002;21:1330.
3. McGinnis JM, Foege WH. Actual causes of death in the United States. JAMA. 1993;270:22072212.
4. US Department of Health and Human Services. Healthy People 2010: Understanding and Improving Health. Washington, DC: US Department of Health and Human Services; 2001.
5. Keller EF. The Century of the Gene. Cambridge, Mass: Harvard University Press; 2000.
6. Strohman R. Ancient genomes, wise bodies, and unhealthy people: limits of a genetic paradigm in biology and medicine. Perspect Biol Med. 1993;37: 112145.[Web of Science][Medline]
7. Tanner CM, Ottman R, Goldman SM, et al. Parkinsons disease in twins. JAMA. 1999;281:341346.
8. Breitner JC. Alzheimers disease, National Academy of Sciences National Research Council Registry of Aging Twin Veterans III. Detection of cases, longitudinal results, and observations on twin concordance. Arch Neurol. 1995; 52:763771.
9. McGue M, Vaupel JW, HoIm N, Harvald B. Longevity is moderately heritable in a sample of Danish twins born 18701880. J Geront Biol Sci. 1993; 48:32373244.
10. Finch CE, Tanzi RE. Genetics of aging. Science. 1997;278:407411.
11. Schwartz N. The life and work of Louis Pasteur. J Appl Microbiol. 1991: 91:597601.[CrossRef]
12. Holmes OW. "Songs in Many Keys." Project Gutenberg EBook The Poetical Works of O.W. Holmes, Volume 4. Songs in Many Keys #18 in our series by Oliver Wendell Holmes, Sr. 1893. Available at: http://www2.cddc.vt.edu/gutenberg/etext05/ohp0410.txt. Accessed December 6, 2004.
13. Yates FE. Order and complexity in dynamic systems: homeodynamics as a generalized mechanism for biology. Mathematics and Computer Modeling. 1994;14:4974.
14. Cannon W. Organization for load and its health consequences. Physiol Rev 1922;9:399431.
15. Selye H. The Story of the Adaptation Syndrome. Montreal, Ontatio, Canada, ACTA; 1952.
16. McEwen BS. Allostasis, allostatic load, and the aging nervous system: role of excitatory amino acids and excitotoxicity. Neurochem Res. 2001;25: 12191231.
17. Seeman TE, Singer BH, Rowe JW, Horwitz I, McEwen BS. Price of adaptationPrice of allostatic load and its health consequences. Arch Intern Med. 1997;157:22592268.
18. Bortz W. The disuse syndrome. West J Med. 1984;141:691699.[Web of Science][Medline]
19. Muller LA. Influences of training and inactivity on muscle strength. Arch Phys Med Rehab. 1970;51:449462.[Medline]
20. Kasch FW, Boyer JL, VanCamp S. Cardiovascular changes with age and exercise. Scand J Med Sci Sports. 1995; 5:147151.[Medline]
21. Laukkanen P, Heikkinem EJ, Kauppinen M. Muscle strength and mobility are predictors of survival in 75-year-old people. Age Ageing. 1995;24:465473.
22. Blair SN, Kuhn KW, Barlow CE, Paffenbarger R, Gibbons LW, Macera CA. Changes in physical fitness and all cause mortality. Prospective study of healthy and non-healthy men. JAMA. 1995; 273:10941100.
23. Bortz WIV, Bortz W II. How fast do we age? Exercise performance over time as a biomarker. J Geront. 1996; 51a:223225.
24. SehI M, Yates FE. Rates of senescence between ages 30 and 70 years in healthy people. J Geront. 2000; 13: 198208.
25. Diamond J. Evaluation of biological safety factors: a cost/benefit analysis. In: Weibel ER, Taylor CR, Bolis L, eds. Principles of Animal Design. Cambridge, Mass: Cambridge University Press;1998:2129.
26. Bortz W. A conceptual framework of frailty. J Gerontol A Biol Sci Med Sci. 2002;57:M283M288.
27. Verdery R. Failure to thrive. In: Hazzard RR, Bierman E, Blass J, Ettinger WH, Halter JB, eds. Principles of Geriatric Medicine and Gerontology. 3rd ed. New York, NY: McGraw Hill; 1994: 12051211.
28. International Classification of Impairments, Disabilities, and Handicaps. Geneva, Switzerland: World Health Organization: 1980.
29. White KL, Williams TF. Green-burg BC. The ecology of medical care. N Engl J Med. 1961:265:885892.
30. Green LA, Fryer GE, Yawn BP, Lanier D, Dovey SM. The ecology of medical care revisited. N Engl J Med. 2001:344:20212025.
31. Hogan C. Lunney J, Gabel J, Lynn J. Medicare beneficiaries costs of care in the last year of life. Health Aff. 2001; 20: 188195.
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |