The Shaking Palsy
In Brain Storms: The Race to Unlock the Mysteries of Parkinson’s Disease (Scientific American–Farrar, Straus, Giroux, 2015), Jon Palfreman, a recently retired professor of journalism, writes about early attempts to understand and treat the disease.
“An Essay on the Shaking Palsy” (the 1817 monograph by James Parkinson) is a beautiful piece of medical literature, one that people with Parkinson’s everywhere will recognize captures much of what they go through— including tremor, poverty of movement (also called bradykinesia), and postural instability. “Walking,” Parkinson wrote, “becomes a task which cannot be performed without considerable attention. The legs are not raised to that height, or with that promptitude which the will directs, so that the utmost care is necessary to prevent frequent falls.”
Despite its brilliance, few physicians noticed Parkinson’s essay. As a consequence, 19th-century individuals struck down with the condition were left to figure out matters on their own. One of the most moving stories that I have come across is that of the Prussian linguist, diplomat, and educational reformer Wilhelm von Humboldt (1767–1835). Ignorant of Parkinson’s essay, Humboldt documented his own parkinsonian decline in a series of wrenching letters to a friend, Charlotte Diede. He noted his stooped posture, complained of “an intolerable slowness and clumsiness” when unbuttoning clothes, and reported that his handwriting was shrinking (what’s now called micrographia). In a poignant passage written on November 4, 1833, he laments, “Every line starts, with best intentions, in large letters only to end, with ill success, in barely legible small ones. If my life hadn’t taught me patience and self-control, this would seem to me insupportable.”
Not understanding that he had a neurodegenerative disease, Humboldt interpreted his symptoms as accelerated aging following the death of his wife. After seven years of Parkinson’s symptoms, Humboldt died of pneumonia.
Humboldt joins a list of intellectuals in history who suffered with the symptoms of Parkinson’s disease before the infirmity had been recognized and named. Another was the 17th-century English philosopher Thomas Hobbes. John Aubrey wrote in his Brief Lives that Hobbes “had the shaking palsy in his hands; which began in France before the year 1650, and has grown upon him by degrees, ever since, so that he has not been able to write very legibly since 1665 or 1666, as I find by some of his letters to me.”
The disease that James Parkinson noticed would gain widespread recognition thanks to the 19th-century French physician Jean-Martin Charcot, the second major figure in the history of this disease. In his day, Charcot, a short, stocky figure with a striking resemblance to Napoleon, was a medical celebrity. According to the neuroscientist and historian Christopher Goetz, people came from all over the world to watch Charcot’s clinical lectures at the Salpêtrière Hospital in Paris. Housing 5,000 patients, 3,000 of whom had neurological conditions, the Salpêtrière was a neurologist’s paradise. Whereas James Parkinson had informally looked at just six cases with one common syndrome, Charcot methodically analyzed hundreds of patients with a wide range of odd disorders. He soon discovered several neurologically distinct entities—including multiple sclerosis, amyotrophic lateral sclerosis, Charcot-Marie-Tooth disease (a peripheral nervous system disorder involving loss of touch sensation), and the shaking palsy.
James Parkinson’s 1817 essay was hardly known in France. But sometime in the 1860s, Charcot obtained a copy and immediately realized its importance. By carefully observing his own patients at the Salpêtrière, he codified (more precisely than Parkinson) the disease’s four common symptoms—tremor, rigidity, slowness or poverty of movement, and postural instability—and added two more, which Parkinson had missed: small handwriting (the micrographia that von Humboldt had noticed) and facial masking (hypomimia), in which the patient’s facial expression is lost or diminished because of altered muscle tone.
The perceptive Charcot—whose students included Sigmund Freud and William James—noticed that not all patients had tremor (about one in five patients lacked this symptom). Charcot argued that given this fact, calling the condition the shaking palsy was misleading. He proposed instead the label “Parkinson’s disease”—and it stuck.
By the 1880s, thanks to his extensive clinical research at the Salpêtrière, Charcot had essentially completed the clinical picture of Parkinson’s disease, at least when it came to the motor symptoms. He would have had little difficulty distinguishing those of us at the Palais des Congrès in Montreal who had Parkinson’s from those who didn’t. And in addition to becoming an expert at diagnosing the condition, he started treating patients’ symptoms, such as tremor, with plant-based formulations that he came up with by trial and error. He prescribed hyoscyamine—an extract of jimsonweed—in pill form rolled into bits of white bread. Other medicines were derived from belladonna (deadly nightshade).
Charcot developed other intriguing therapies. Having observed that the symptoms of Parkinson’s patients appeared to improve after long rides in carriages, in trains, and even on horseback, he speculated that the vibrations might be therapeutic. So Charcot developed an electrically powered “shaking chair,” or fauteuil trépidant. One of his students, Gilles de la Tourette, refined this concept into a portable shaking helmet that vibrated the brain. His therapeutic vibration concept was recently tested in a controlled trial using commercially available massage chairs. Patients were assigned to one of two groups: one cohort had daily sessions in a vibrating chair for one month; the other had the same number of sessions in the same chair but with the vibration switched off. Both groups were exposed to relaxing natural sounds, such as ocean waves. The researchers concluded that what Charcot observed was largely a placebo effect, in which perceived benefit had more to do with the patient’s and the clinician’s wishful expectations of improvement than the vibrational therapy.
We can thank Jean-Martin Charcot, then, for clinically defining, naming, and even attempting to treat the disease. In reality, however, in Charcot’s day, Parkinson’s was not yet a disease in the true sense of the word, but merely a cluster of symptoms or, in medical parlance, a “syndrome.” Before a syndrome can be classified as a true disease, physicians need to possess at least one of two additional pieces of knowledge: how the malady started or how it ends. Knowing a syndrome’s cause is the clearest sign you have a real disease—as occurred when scientists discovered that the human immunodeficiency virus (HIV) caused acquired immunodeficiency syndrome (AIDS). If a cause is unknown, then physicians and scientists hunt for specific pathological changes in the patient’s tissues, which, in the case of the brain, are usually detected in a postmortem examination after the patient dies.
In the 1880s, scientists had little idea what caused parkinsonism, but pathologists routinely dissected patients’ brains looking for signs of damage to various tissues. Charcot, originally trained as a pathologist, taught the “anatomo-clinical” method, which sought to connect the clinical features of a disease like Parkinson’s to anatomical changes or “lesions” in the brain.
In a typical postmortem dissection at the Salpêtrière, a pathologist peeled back the face, cut open the top of the skull, and removed the brain (quite similar to how a postmortem dissection would be performed today). But thereafter, all he had to guide him was the gross appearance of the brain’s “white” and “gray” matter. The upper portion of the brain—the cerebral hemispheres—looks a bit like the cap of a mushroom, and the rest of the brain resembles its stem. The mushroom cap is split by a deep canyon (dividing the left and right hemispheres) and covered by a wrinkled outer layer of gray matter called the “cortex” (the Latin word for “bark”). Underneath the cortex is largely white matter punctuated with islands of gray matter. When Charcot’s pathologists sawed into the brain horizontally (slicing from the top to the bottom) or coronally (going from the back to the front), they observed different brain structures, which earlier anatomists had assigned Latin names—ventricles (bellies), corpus callosum (tough body), corpus striatum (striped body), globus pallidus (pale globe), thalamus (inner chamber), and substantia nigra (black stuff). This last structure was so named because its cells contained the pigment melanin, making them dark.
The anatomo-clinical method depended on finding differences between the brains of healthy and sick individuals. Because most impoverished Salpêtrière patients were wards of the state, autopsies were commonplace, so Charcot and his colleagues had numerous opportunities to find odd lesions in deceased patients’ brains that might explain the neurological symptoms they suffered in life. One day in 1893 (the same year that Charcot died), two of Charcot’s students, Paul Blocq and Georges Marinesco, got a lucky break. They admitted to the Salpêtrière a 38-year-old patient with a parkinsonian tremor and rigidity on the left side of his body. The patient subsequently died of pulmonary complications and was autopsied. The postmortem turned up a hazelnut-sized lump in the right side of his midbrain, very close to the substantia nigra. Blocq and Marinesco’s discovery inspired Édouard Brissaud, Charcot’s successor at the Salpêtrière, to hypothesize that the substantia nigra—the site of the black stuff—was the key pathological source of Parkinson’s disease.
Was this a meaningful finding or just coincidence? For 25 years, no one bothered to systematically investigate the matter. Then, in 1919, Constantin Tretiakoff, a Russian graduate student working in Paris, offered convincing proof that the black stuff was indeed associated with Parkinson’s disease. His dissertation examined 54 autopsied brains, nine of which had Parkinson’s. Tretiakoff found that all the genuinely parkinsonian brains showed extensive damage to the substantia nigra, whereas none of the healthy controls did. The difference between normal and parkinsonian brains could scarcely have been clearer: the diseased brains had simply lost their black stuff. Tretiakoff also noticed something else. Some of the brain cells of deceased Parkinson’s patients contained small spherical structures. They were roughly the size of a red blood cell and were surrounded by a clear halo. Tretiakoff named them “corps de Lewy,” or “Lewy bodies,” to acknowledge their discoverer, Frederick Lewy, a German pathologist working in Dr. Alois Alzheimer’s Munich laboratory.
Pathologists and neurologists would in time come to accept that Lewy bodies were the defining hallmark of genuine Parkinson’s disease. Neurologists might diagnose parkinsonism in life. But only after pathologists found Lewy bodies in a patient’s damaged substantia nigra after death would they be sure that he truly had Parkinson’s disease.
Although scientists still had no idea what caused Parkinson’s, it could now fairly be called a disease rather than a syndrome. By the 1950s, more than 130 years after James Parkinson’s essay, scientists—especially Charcot, Tretiakoff, and Lewy— had established the commonly known features of the Parkinson’s brand. This brand framed the disease as a “movement disorder,” mostly found in the elderly, and resulting from damage to a very small region of the brain—the substantia nigra.
So far, little had been found to effectively treat the condition, but that was about to change, thanks to the efforts of a group of brilliant Swedish and Austrian researchers. They proved that it wasn’t only the black stuff that vanished when neurons died in Parkinson’s patients. Something else disappeared as well—a brain chemical called dopamine.
Jon Palfreman, retired KEZI professor of journalism, is a Parkinson’s patient and has made the disease his journalist beat.
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