Over time, the average human lifespan has increased, but the maximum lifespan has not. Despite all our medical advances, we can’t live past approximately 115 years. But why is it that, after millions of years of evolution, our bodies are still so flawed? Why do we get disease at all? Why hasn’t natural selection prevented heart attacks, nearsightedness, and Alzheimer’s disease?
In Why We Get Sick, psychologist Randolph Nesse and evolutionary biologist George Williams argue that disease is an inevitable side effect of evolution: Each of the strengths we’ve developed through natural selection has an aspect that also brings illness. Published in 1995, their theories have been credited with launching the field of evolutionary medicine, shedding light on the factors behind disorders ranging from allergies to Alzheimer's to cancer.
What people call aging is biologically termed senescence—the bodily deterioration accompanying age. Evolutionary biologists seek to understand why our bodies wear out by considering the role of natural selection. They approach the question through Darwinian principles, arguing that if something seems like a maladaptation of the body or an error in natural selection, we’ve probably missed something—evolutionary changes typically arise to resolve problems, not to create them.
When identifying the factors behind diseases, scientists distinguish between proximate causes and evolutionary causes.
Evolutionary explanations of disease seek to account for the evolutionary adaptation that has led to the disease, and to explain how that adaptation proffers an advantage that outweighs its disadvantages.
A common line of inquiry is to ask whether disease is caused by genetics or the environment. In some cases, it’s clearly one or the other. But in many cases, both genes and the environment are insufficient by themselves. Instead, they interact together to produce a disease.
As we examine why evolution prefers some genes over others, keep in mind that natural selection doesn’t function by considering genes in isolation: The determining factor in whether a gene is favored is whether or not it helps an organism thrive in its environment. The influence of genetics and environment on health are therefore intricately connected. In one setting, a certain gene might confer significant advantage, but change the environment, and it may no longer increase the organism’s fitness. As we’ll discuss later, this may be the case for a variety of genes that lead to disease in our modern environment, like heart disease.
Evolutionary medicine is not just philosophizing; it can help predict what to expect when treating disease, and it can guide our choices as to how vigorously we should treat certain symptoms.
For example, infections usually cause low iron levels. The proximate viewpoint would suggest that giving iron as a treatment is an obvious choice. However, the evolutionary viewpoint would question, “Is lower iron perhaps a defense against infection? Perhaps the body has adapted to lower iron during an infection, because it helps fight the infection? If this is true, wouldn’t giving iron actually worsen the infection?”
Natural selection is often thought of informally as “survival of the fittest,” but this doesn’t mean fitness in the everyday sense of good health and long life. In Darwinian terms, higher fitness means more reproduction and a greater number of viable offspring.
Thus, natural selection will favor genes that increase an individual’s reproduction, even if they reduce longevity. Studies support this theory: Animal experiments show that increasing lifespan causes lower and later reproduction, suggesting there’s a tradeoff between longevity and vigor. For example, mice on caloric restriction extend their lifespans, but they don’t reproduce. They stay suspended in a pre-reproductive state waiting for adequate food supply.
Another consequence of evolution’s focus on reproductive health is that natural selection won’t be concerned either way with genes that kill or debilitate you after you’ve raised kids to independence. Evolution doesn’t bother to either promote or filter these genes out, since they don’t affect reproduction. This phenomenon can be seen in the example of Huntington’s Disease, which is an intimidating disease—patients die between ages 40-60. But, because it causes no apparent harm before age 40, affected patients have generally already made their reproductive contributions to the species, so the disease faces little selection pressure.
In the following sections, we’ll explore some of the evolutionary causes behind disease and other bodily disorders that Nesse and Williams outline. We’ll look at why many diseases are the unintended consequences of once-beneficial adaptations, why symptoms of diseases are beneficial adaptations themselves, how evolutionary...
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After millions of years of evolution, why do our bodies still seem so flawed? Why do we get disease at all? Why hasn’t natural selection prevented heart attacks, nearsightedness, and Alzheimer’s disease?
The common answer is that “natural selection isn’t powerful enough to get rid of disease.” This is usually the wrong idea.
Instead, it’s important to realize that the body is a bundle of careful compromises. The reason we have diseases today is that the very things that cause disease were helpful for us at one point, or are still helpful for us in certain situations. In this way, evolutionary medicine seeks to understand why we have disease.
In thinking about disease, it’s important to distinguish between proximate causes and evolutionary causes of disease.
Natural selection is often thought of informally as “survival of the fittest,” but this is a confusing phrase. People often have the wrong idea of what “fitness” means. It doesn’t mean fitness in the everyday sense of good health and long life.
In Darwinian terms, a higher fitness means more reproduction and a greater number of viable offspring. If a gene leads to production of more viable offspring in future generations, that gene will be enriched in the population. Likewise, if a gene codes for characteristics that result in fewer viable offspring in future generations, that gene is gradually eliminated.
Taking the phrase “survival of the fittest” again, we now see that “survival” is important for natural selection only insofar as it increases reproduction. If a gene helps an individual survive longer, but at the expense of having fewer offspring, that gene will show up less often in the gene pool.
Genes that increase lifetime reproduction will be selected for, even if they reduce the individual’s longevity.
This is one reason that we haven’t evolved away common diseases—the genes that cause gout and dementia later in life may actually increase our...
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The war with bacterial and viral pathogens has gone on for millions of years and continues today. Our body has evolved defenses to combat infections, and in turn the pathogens evolve ways to overcome these defenses.
As previously described, the body is a collection of compromises. Maintaining the defenses at all times would be too costly—there’s no need to raise defenses when there are no pathogens around.
When the defenses do activate, they sometimes cause symptoms that appear to be the disease. In reality, the symptoms are the defense mechanisms at work. If this hypothesis is true, then treating these symptoms can counter-intuitively aggravate and lengthen the infection. Here are a few examples:
As discussed, hosts and pathogens adapt to each other in continuous cycles. One strategy is quickly defeated by a counterstrategy. This gives rise to the Red Queen Principle, named after the statement in Alice in Wonderland: “It takes all the running you can do, just to keep in the same place.”
Antibiotics were one of the great medical successes of the 20th century. However, due to widespread use, increasingly bacteria are evolving...
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Jerry McPheePain and fear are often considered negative conditions to be avoided. But both pain and fear serve vital functions in survival. Pain signals that tissue is damaged; fear signals that danger might be nearby, and so caution is warranted.
Both pain and fear are useful to avoid injury. Blocking either can worsen damage. People who lack the capacity to feel pain almost all die by age thirty; people born without fear tend to end up in the emergency room or the morgue.
Fear of some things is innate, since that mistake even once is very costly. A rabbit is born to be afraid of foxes, since slipping up once can cost a rabbit its life. But innate behavior is inflexible—it can’t mold to new situations that would merit more appropriate responses.
More flexibly, other fears can be learned so as to be situationally useful. A fawn might stare blankly at an approaching wolf until its mother flees. Then the fawn learns that wolves are probably bad and should be run away from, and the fawn passes this lesson to her children. These types of fears are not hardwired; they can be unlearned, and they can be extinguished when the cue is removed.
Humans have the...
Just like animals, plants undergo natural selection for reproductive fitness. In the wild, plants develop defenses from eating, like hard pods and toxins.
Plants have developed a wide range of toxins, including tannins (in wine), alkaloids, cyanide, glycosides (from foxgloves), [restricted term] (from potatoes), and solanidine (nightshades, potatoes). While the amounts of toxins in typical plants aren’t enough to damage humans, consider how much they might deter a hungry mouse weighing 1/3000th of a human’s weight.
If you’re ever foraging for plants in the forest, you obviously would like to know which plants are toxic and not. Darwinian thinking is helpful here: consider the natural competitive equilibrium that would result in the phenotype observed.
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We now return to a question asked earlier in the summary: Why haven’t we evolved away genes that cause disease?
You now know a few reasons: the disease-causing gene may have benefits that are not as obvious. Also, the gene may have been beneficial during the Stone Age, but only cause disease in today’s environment (we’ll cover this explanation more later in the chapter).
Here are even more reasons that we haven’t evolved away genes that cause disease:
What people call aging is biologically termed senescence, the bodily deterioration accompanying age. Human organ systems tend to wear out at the same rate, on average. Maintenance and repair systems lose their efficacy, and old people become progressively more vulnerable to diseases and injuries.
Senescence has been stable over time. Over the past centuries, the average human lifespan has increased, but the maximum lifespan has not. Despite all our medical advances, humans cannot live past about 115 years.
Theoretically it would be a huge reproductive advantage to maintain health for more time - imagine humans who lived to be 300 and reproduced for 100 years. Why haven’t humans evolved to live longer?
Early theories suggested senescence was necessary to make room for the young. But as we’ve learned with lemmings in Chapter 2, natural selection doesn’t occur on the group level. It’s also prone to exploitation by individuals who don’t follow the same strategy—the gene that caused individuals to reproduce rapidly and live longer would overtake the population.
Later theories, in line with our other explanations of why genes persist, suggest that **genes that promoted...
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Evolution makes incremental changes on what came before. It does not totally scrap a current design and start from scratch. This can lead to some historical artifacts that cause problems today, and that we might redesign should we have the choice.
For example, in all vertebrates, the esophagus (leading to the stomach) and the trachea (leading to the lungs) have the same input (the mouth). This can lead to choking. This arrangement came from an early wormlike ancestor that used the same tube for both respiration and digestion. All vertebrates descended from this ancestor and inherited this design.
In contrast, insects and mollusks have complete separation of the breathing and eating structures. They evolved on a different lineage and aren’t beholden to this evolutionary artifact.
Here are more examples of evolutionary legacies:
(Shortform note: The ideas in Chapter 10 were integrated into previous chapters, so our summary is skipping to Chapter 11.)
Allergies show such a strong reaction, are so inconvenient, and form a system of such complexity that, per evolutionary medicine principles, it seems unlikely they have no useful function to compensate, else they’d have been selected out.
Briefly, how do allergies work? They are the consequence of a series of steps upon exposure to a foreign substance:
IgE makes up just 1/100000 of the total antibody in blood, but it produces an outsized response. In an allergy, 10% of IgE may be specific to the antigen, such as pollen;.
The function of allergy is unclear, though there are a few leading hypotheses:
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Cancer arises when normal mechanisms for cell growth go awry.
The human body has 10 trillion cells, many of them replenishing themselves. With each division of a cell, mutations in genes are introduced. Given all this activity, it’s really a wonder that we’re typically protected against cancers for decades at all.
Cells have a number of mechanisms to prevent cancers:
The relationship between...
There are perhaps few mysteries as intriguing and perplexing as the courtship between females and males. Darwinian thinking has explanations for this too.
Some animals reproduce asexually, with mothers essentially giving birth to a clone of itself. Why do mammals and humans go through all the trouble of sexual reproduction?
The classical explanation is that sexual reproduction promotes genetic diversity, through the combination of genetic material from the mother and father. Having more genetic diversity avoids over-optimization to one genome, and it promotes survival in changing environments.
In comparison, a woman who could bud off offspring without sex may have a short-term advantage in producing offspring, but the entire enetically identical clan may be wiped out in one calamity. If ten thousand clones of one woman are all especially vulnerable to influenza, they may all die in one epidemic, whereas a genetically diverse population would only lose a fraction of its members.
Different animals have different reproductive strategies. They vary in these factors:
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The field of psychiatry has tried to codify mental illness through clear-cut symptoms, rather than as gradations of emotions that are influenced by psychology and life experiences. Patients also understand their mental illness as imbalances in brain chemicals; they might be offended if the psychiatrist insisted that their illness were just a maladaptive psychological process.
The authors argue that ignoring the underlying function of emotions is like ignoring physiology in medicine.
As an analogy to today’s approach to psychiatry, imagine if we investigated “cough disorder,” creating objective criteria for diagnosis and subtyping (like coughing more than twice per hour). We then discover a cough center in the brain and muse about what dysfunctions lead to coughing, then investigate genetic causes for people prone to coughing.
This is clearly silly, but only because we know cough is a defense. We know not to look for causes of cough in the nerves and muscles, but rather upstream in the stimulus that provokes a cough (like the common cold).
Emotions are no different. They provide a valuable function to us in everyday life. Understanding this normal function should give us...
The human body has been shaped over millions of years as a well-functioning bundle of compromises. What looks like mistakes in evolution more likely continue to exist for these reasons:
The authors wish to broaden discussions of disease to include these questions:
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Reflect on what you've learned about the evolutionary causes of disease.
What were your most surprising takeaways from what you learned in this book?