Showing posts with label cortisone. Show all posts
Showing posts with label cortisone. Show all posts
Wednesday, September 21, 2011

Today in Medical History

Synthesized Cortisone

In 1948, Edward Kendall and Philip Hench created the first of the many “miracle drugs," which were actually synthesized hormones, to treat rheumatoid arthritis and other diseases. Hench and Kendall, who each headed a medical department at the Mayo Clinic in Rochester, Minn., realized that the adrenal glands play an important role in rheumatoid arthritis. The two noticed that a woman with rheumatoid arthritis had a lessening of symptoms while she was pregnant, and they worked to discover what caused the change. They were able to isolate a hormone in the cortex, or outer part, of the adrenal glands, which they called cortisone.

On Sept. 21, 1948, Hench administered a synthesized version of cortisone developed by Kendall to a patient with arthritis. The two researchers were awarded the Nobel Prize in physiology or medicine in 1950 for their achievements.

Tuesday, December 22, 2009

(Addison’s) A piece of presidential history solved the puzzle

By Sandra G. Boodman
Special to the Washington Post
Tuesday, December 15, 2009

 

As she lay in a heap, trying to figure out how badly she had hurt herself falling headfirst down a flight of stairs in the middle of the night, Rebecca Woodings grasped just how sick she really was.

 

For months doctors had been ratcheting up the medicines used to treat her intractable allergies. At one point she was taking 10 drugs a day and getting allergy shots. An economist who works for a large Washington law firm, Woodings, 49, told doctors she was tired; she assumed her fatigue was a consequence of her allergies, which were also causing a persistent cough. She did not tell them she was so exhausted she had to sit on the sidewalk while waiting for a bus and couldn't stand long enough to cook a meal.

 

Hours before she tumbled down the stairs of her Takoma Park home last June, an astute pulmonologist had figured out what was wrong -- and it had nothing to do with her lungs. That night, as Woodings tried to move the wrist she had broken in the fall, she focused on her 6-year-old son, realizing that if she had smacked her head she could have died. "I kept thinking, what would have happened to my child?"

 

In the fall of 2008 Woodings began feeling unusually tired. Walking less than a mile to the Metro in the morning made her break into a sweat. "It was very tiring," she said, and she recalled feeling puzzled. "I'm not terribly out of shape and I'm not overweight." Once on the Metro, Woodings made sure to get a seat; standing for 20 minutes was unthinkable.

 

During her annual checkup in November, her long-time internist at George Washington University discovered a Vitamin D deficiency and prescribed a short course of high-dose supplements.

 

By December, the fatigue was worse. Woodings had to sit down in the middle of a hymn during a church service. "All these little white-haired people around me are standing, and I couldn't," she recalled. When she mentioned the incident to a friend who works at the National Institutes of Health, she was told the symptoms sounded like a heart attack. Alarmed, Woodings immediately headed to a nearby emergency room, where an EKG and a chest X-ray showed that her heart was fine and her lungs were clear. Her father, a retired physician, suggested that maybe an antihistamine was causing her fatigue. Woodings stopped taking it and felt slightly more energetic.

 

By February, she was forced to sleep propped up on pillows and was taking a prescription cough syrup, which had little effect. The mother of a typically energetic kindergartner, she had started falling into bed around 8:30, when her son did. One night, she was so tired she told him to put himself to bed and crawled into bed at 8. Her allergist began administering allergy shots, which didn't help. Another doctor -- not her regular internist -- suggested she cut back on her sleep and get more exercise. Woodings replied that she was so tired she worried she might fall off a treadmill.

 

Routinely she arrived at the office at 9 a.m., already worn out. "It's really difficult to talk about being exhausted at a law firm," she said. "It sounds wimpy," so she didn't mention it.

 

In March, when she was handed a demanding new assignment with multiple deadlines, two new symptoms surfaced: Woodings began retching unpredictably -- "that damn cough," she remembered thinking -- and developed ferocious leg cramps at night. By then she noticed another peculiarity: Although she literally could not stand long enough to wait for a light to change while crossing the street, she could manage if she kept moving, walking slowly in a circle.

 

In early April, she went back to the allergist. He diagnosed a bad sinus infection and doubled the medications she was taking to 10 per day, including a short course of prednisone, a corticosteroid sometimes used to treat severe sinus infections.

 

After the first day, Woodings said, she felt markedly better. A week later the cough had disappeared and her energy slowly returned.

 

But by Memorial Day the fatigue was back and Woodings realized her problem wasn't allergies. She had stopped taking the allergy drugs, deciding that they might be the cause; her cough was gone. Woodings called her internist, whom she had not seen in six months. The doctor was heading out of town and Woodings decided to wait until her return rather than see a covering physician. In the meantime her physician ordered several tests, including those for Lyme disease and HIV, as well as CT scans of her lungs and sinuses.

 

On June 5, Woodings was told she had a possible bacterial infection in her lungs -- but not tuberculosis -- and was referred to GWU pulmonologist Susan Hasselquist. When she called to make an appointment, she was told that Hasselquist's first opening was a month away.

 

Desperate, Woodings decided to lie. "I said, 'I can't wait. The potential diagnosis is active TB.' " She was given an appointment for the next day.

 

On June 10 Woodings met with Hasselquist, who listened intently as Woodings recounted the events of the previous seven months. Unable to obtain a blood pressure using an automated cuff, Hasselquist measured it manually and found it was an alarmingly low 90/55. The lung specialist recalled being struck by how weak Woodings was: She lay down on the examining table while they talked because sitting up was too tiring. Hasselquist said she kept thinking of, and discarding, possible diagnoses. "I knew if we just kept talking I'd figure it out," she said.

 

Her eureka moment occurred when she zeroed in on Woodings's deep tan and asked her about it. Woodings, who is normally very fair, said that other people had remarked on it and that she hadn't spent much time in the sun.

 

Suddenly, Hasselquist said, she was certain what was wrong, a hunch triggered by photographs she'd seen of a ruddy-looking President John F. Kennedy, who had Addison's disease, a rare endocrine disorder that occurs when the adrenal glands become damaged and fail to produce enough cortisol and aldosterone, hormones vital for metabolic function. Most cases are the result of an autoimmune attack in which the immune system slowly destroys the adrenal glands. Woodings's dramatic improvement while taking prednisone, the steroid prescribed to treat her sinus infection, was a vital clue: It is one of the medicines used to treat Addison's.

 

Kennedy received an Addison's diagnosis at age 30; his sister, the late Eunice Kennedy Shriver, is also believed to have suffered from the disorder, which affects one to four of every 100,000 people, according to the National Institute of Diabetes and Digestive and Kidney Diseases.

 

Woodings had the classic symptoms of Addison's: progressive fatigue, muscle weakness, low blood pressure that falls further during a change in positions, and hyperpigmentation, which resembles a dark tan. The retching and legs cramps are also symptoms, although her allergies and cough are not.

 

Hasselquist did not mention her suspicion to Woodings because it would require confirmation from an endocrinologist. She said she suggested hospitalizing Woodings because she was so weak. When Woodings declined, Hasselquist warned her against standing up too quickly, which could cause dizziness.

 

After the appointment with Hasselquist, Woodings went straight home, ordered a pizza and went to bed. She awoke several hours later and headed for the bathroom to urinate. She remembers feeling dizzy, and then realizing she was at the bottom of the stairs, her wrist shattered. She managed to get up, call 911 and wake her son. Doctors in the ER set her wrist, told her to see an orthopedist because she would need surgery, then sent her home.

 

A few days later GWU endocrinologist Michael Irwig, to whom Hasselquist referred Woodings, confirmed the Addison's diagnosis. He prescribed prednisone and another drug Woodings will have to take for the rest her life to replace the hormones her body no longer produces.

 

Within a few weeks, Woodings said, she felt much better. Her energy level returned to normal, as did her blood pressure. Her tan is fading, and surgery on her wrist was successful.

 

"I can't fault any of the doctors," Woodings said, adding that she believes she should have called her internist early on, instead of consulting other physicians. "I think I could have described my condition a little better. I never said, 'I have to sit on the sidewalk waiting for a bus,' but rather, 'I'm tired all the time.' "

 

If you have a Medical Mystery that has been solved, e-mail medicalmysteries@washpost.com. To read previous mysteries, go to http://www.washingtonpost.com/health.

 

From http://www.washingtonpost.com/wp-dyn/content/article/2009/12/14/AR2009121402863.html

 

~~~~~~~~~~~~~~~

 

Feedback:

Woman's tale of Addison's disease proves the value of primary-care physicians

 

Tuesday, December 22, 2009

 

Of primary importance

 

"A piece of presidential history solved the puzzle" [Dec. 15], about the lady found to have Addison's disease, points out how crucial it is to have a primary-care focus in evaluating patients. Often patients scramble through a maze of specialists, as she did, without a strong primary-care clinician coordinating care.

 

My hope is that health reform will recognize the essential perspective that primary-care physicians from family medicine, geriatrics and internal medicine bring to patient care. They can save patients and the health-care system heartache and money. It is the most challenging field in medicine and the most holistic.

 

Our system should provide incentives for new medical school graduates to join these fields and reward these physicians appropriately. These doctors work very, very hard. Good primary-care clinicians are worth their weight in gold.

 

Christine Butler

Coordinator, Palliative Care Service

Sibley Memorial Hospital

Washington

 

From http://www.washingtonpost.com/wp-dyn/content/article/2009/12/18/AR2009121803706.html

Tuesday, October 13, 2009

Hydrocortisone Dosing during Puberty in Patients with Classical Congenital Adrenal Hyperplasia: An Evidence-Based Recommendation

Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2009-0942
The Journal of Clinical Endocrinology & Metabolism Vol. 94, No. 10 3882-3888
Copyright © 2009 by The Endocrine Society

Hydrocortisone Dosing during Puberty in Patients with Classical Congenital Adrenal Hyperplasia: An Evidence-Based Recommendation

Walter Bonfig, Susanne Bechtold Dalla Pozza, Heinrich Schmidt, Philipp Pagel, Dietrich Knorr and Hans Peter Schwarz

University Children’s Hospital (W.B., S.B.D.P., H.S., D.K., H.P.S.), Ludwig Maximilians University, Division of Pediatric Endocrinology, D-80337 Munich, Germany; and Division of Bioinformatics (P.P.), Technical University, D-80337 Munich, Germany

Address all correspondence and requests for reprints to: Walter Bonfig, M.D., University Children’s Hospital, Division of Endocrinology, Ludwig Maximilians University, Lindwurmstr. 4, D-80337 Munich, Germany. E-mail: walter.bonfig@med.uni-muenchen.de.

Context: Patients with congenital adrenal hyperplasia (CAH) are at risk for early pubertal development and diminished pubertal growth. Liberal treatment with glucocorticoids will prevent early puberty but may inhibit growth outright.

Objective: The aim of the study was to determine an optimal range for hydrocortisone dosing during puberty in children with classical CAH who were exclusively treated with hydrocortisone.

Methods: The effects of glucocorticoid treatment for classical CAH were retrospectively analyzed in 92 patients (57 females). Growth pattern, final height (FH), and mean daily hydrocortisone dose were recorded.

Results: Pubertal growth was significantly reduced in all patients: salt-wasting (SW) females, 13.8 ± 7.4 cm; simple virilizing (SV) females, 13.1 ± 6.2 cm; vs. reference, 20.3 ± 6.8 cm (P < 0.05); and SW males, 17.7 ± 6.7 cm; SV males, 16.2 ± 5.7 cm; vs. reference, 28.2 ± 8.2 cm (P < 0.05). Decreased pubertal growth resulted in FH at the lower limit of genetic potential (corrected FH in SW females, –0.6 ± 0.9; SV females, –0.3 ± 0.9; SW males, –0.8 ± 0.8; and SV males, –1.0 ± 1.0). During puberty, mean daily hydrocortisone dose was 17.2 ± 3.4 mg/m2 in females (SW, 17.0 ± 3.3; SV, 17.4 ± 3.5) and 17.9 ± 2.5 mg/m2 in males (SW, 17.4 ± 2.0; SV, 18.7 ± 3.1). In a logistic regression model, a significant correlation between hydrocortisone dose and FH was found (P < 0.01), and the positive predictive value for short stature rose from below 30% to above 60% when hydrocortisone dose exceeded 17 mg/m2.

Conclusion: With conventional hydrocortisone treatment, pubertal growth is significantly reduced in both sexes, resulting in a FH at the lower limit of genetic potential. These deleterious effects on pubertal growth can be reduced if hydrocortisone does not exceed 17 mg/m2.

From http://jcem.endojournals.org/cgi/content/abstract/94/10/3882

Tuesday, July 14, 2009

From 1960...

The Candidates' Health

RECOVERING from his heart attack and his ileitis surgery, President Eisenhower set a precedent in the 1956 election campaign by frankly discussing the state of his health. Last week the Democrats picked up "the health issue" and were playing hard politics with it among themselves. Jack Kennedy began the intramural scrap by declaring that the presidency demands "the strength and health and vigor of ... young men." Supporters of Lyndon Johnson leaped to the conclusion that Kennedy was making a not-so-subtle allusion to L.B.J.'s 1955 heart attack. "Citizens-for-Johnson" Director John B. Connally countercharged that Kennedy secretly suffers from Addison's disease, an incurable but now controllable deficiency of adrenal secretions. And Johnson-lining India Edwards, former vice chairman of the Democratic National Committee, said: "Doctors have told me that [Kennedy] would not be alive were it not for cortisone."

 

The medical facts:

 

Jack Kennedy, 43, says that he did have a "partial adrenal insufficiency." He laid it to a war-born case of malaria, which itself required treatment through 1949. To supplement adrenal output, Kennedy took regular doses of cortisone from 1947 to 1951 and again from 1955 to 1958. He still takes oral doses of corticosteroids (cortisone-type medication) "frequently, when I have worked hard," although a recent test showed his adrenals to be functioning normally. Whether his is an arrested case of Addison's disease or a borderline adrenal insufficiency is unclear. In two years of almost ceaseless campaigning, Kennedy has displayed remarkable energy and none of the classic symptoms of advanced Addison's disease: chronic fatigue, weight loss, low blood pressure, anemia, or a bronzelike darkening of the skin.

 

Kennedy's earlier medical history is complex. Severe and recurring jaundice forced him to leave Princeton during his freshman year (when his health improved, he later went to Harvard). The Army rejected him because of a football injury to his back, but the Navy accepted him. The back was reinjured when a Japanese destroyer knifed through Lieut. Kennedy's PT boat in 1943. He spent most of 1944 in a Navy hospital, underwent a spinal disk operation, which was not fully successful. As a consequence, in October 1954, surgeons performed a delicate fusion of spinal disks. Slow to heal and set back by relapses that were complicated by the adrenal shortage, his condition became so grave that his family was summoned to his bedside. He had a third spinal operation the following February to remove a metal plate. Last rites were administered. But this time, after two weeks abed, recovery was rapid. Total time spent in the hospital or convalescing: seven months. Today, the only vestige of the spinal problem is that he still sleeps on a board, wears a light corset. Last week, at Kennedy's request, his two Manhattan physicians reported: "Your health is excellent."

 

http://www.time.com/time/magazine/article/0,9171,869575,00.html

Saturday, April 25, 2009

Adrenal Alerts, 4/25/09

Remember  my usual disclaimer!

Honoring an inspiration
Galesburg Register-Mail - Galesburg,IL,USA
By TOM LOEWY Right now she is a 15-year-old girl fighting adrenocortical carcinoma, an aggressive cancer originating in the cortex of the adrenal gland. ...
See all stories on this topic

 

Pharmacy giving hormone talks
Canada.com - Don Mills,Ontario,Canada
Adrenal Fatigue can often mirror symptoms of menopause. The adrenal gland makes up for other endocrine deficiences in the body and will often become over ...
See all stories on this topic

 

From Chaos to Consilience
Psychiatric Times - New York,NY,USA
For example, having a tumor in the thyroid complicates understanding of what a pancreatic or adrenal tumor is doing, and vice versa. ...
See all stories on this topic

 

Aldosterone Provides New Treatment for Age-Related Hearing Loss
Natural News.com - Phoenix,AZ,USA
Aldosterone is a steroid hormone from the mineralocorticoid family, produced in the adrenal cortex. It regulates kidney function and plays a role in ...
See all stories on this topic

 

Beware of too much potassium
St. Augustine Record - St. Augustine,FL,USA
Nonfunctioning adrenal glands and red blood cells breaking up in the circulation can cause potassium elevation. You can do nothing on your own about these ...

 

Lower Levels Of Vitamin D Linked To Asthama Severity In Kids
TopNews - Noida,Uttar Pradesh,India
... with augmented hyperreactivity and were likely to have utilized more inhaled adrenal cortical steroids, all symptomatic of higher asthma harshness. ...

Our Tortured Soul
Cornell University The Cornell Daily Sun - Ithaca,NY,USA
Your lungs scream for air, your nerve synapses fire in a panic to the adrenal glands and release a painful adrenaline rush, brutally increasing your heart ...

 

Life-wise
Wellington Advertiser - Wellington,ON,Canada
The internist explained: "Exercise or tension causes an adrenal rush, which should energize your muscles. But it does the opposite, causing muscles to ...

Community Calendar: Del Mar
Del Mar Times - Del Mar,CA,USA
-Wellness 101 lecture on thyroid and adrenal hormones: 6:45 to 8: 45 pm Stratford Inn, 710 Camino Del Mar. Free. To sign up, call 481-9854 or e-mail ...

Wednesday, January 07, 2009

Addison's Disease and two of its famous sufferers

From http://www.abc.net.au/rn/science/ockham/stories/s18569.htm

with Robyn Williams
on Sunday 31/01/1999

Addison's Disease and two of its famous sufferers
Summary:
John F. Kennedy and Jane Austin both had Addison's Disease. While John F. Kennedy survived the disease, Jane Austin died from it.

Transcript:

Robyn Williams: This week Ockham's Razor is presented by one of its great stalwarts: Dr Jim Leavesley, a great expert in the indispositions of the famous. He's now retired in the beautiful Margaret River south of Perth. Jim.


Jim Leavesley: It is not now fashionable in medical circles to call diseases by their eponymous names. To do so is said to be confusing to those not in the know. So pathologically descriptive names are used, the Greek or Latin bases which are supposed to be universally understood.


For we old fogies, the passing of a named disease is a pity, for not only do we honour the person who first described the condition, but eponymous names are often much more mellifluous than dry descriptive tags. For instance, it is much more satisfying to say someone has Charcot Marie Tooth syndrome, or von Recklinghausen's Disease, rather than the politically correct peroneal muscular atrophy or multiple neurofibromatosis.


But one or two have slipped through the net. Meniere's syndrome, Alzheimer's disease, Parkinson's disease, spring to mind as well as the one I wish to look at in conjunction with two of its victims, Addison's disease.


In 1795 at Long Benton, a village just outside Newcastle-on-Tyne, in northern England, the wife of the local grocer, Joseph Addison, was delivered of a second son. They called him Thomas.


A bright lad, he went on to Edinburgh to do medicine and qualified in 1815. From thence to Guy's Hospital, London, where he became an assistant physician in 1824 and the full works in 1837.


He was a contemporary of Richard Bright, of Bright's disease, and of Thomas Hodgkin, of Hodgkin's disease. What a trio.


Anyway, whatever mental jousting went on, it did not lift Addison's mood, for he was a chronic depressive. He made several attempts on his life until in 1860, he retired to Brighton, disturbed enough to have need of two constant attendants. Despite the care, within months he managed to elude them, flung himself down a stairwell and died of a fractured skull.


But let's go back a bit. On 15th March 1849, Addison had read a paper to the South London Medical Society entitled 'A Remarkable Form of Anaemia'. He cited three cases of increasing lethargy, but made no mention of those characteristic features we associate with his disease, skin pigmentation and low blood pressure. He didn't know how to measure that, anyway. He did note, however, that at post mortem there was a disease of the suprarenal glands, situated just above the kidney.


He did not connect the anaemia and suprarenal condition and said he had stumbled on a second condition, which he called 'melasma suprarenale.' It is this we now call Addison's disease. However, it did show for the first time that the adrenals were necessary for life, and it has been said that the whole of endocrinology dates from 15th March, 1849.


He did not publish until 1855, by which time he had separated the two anaemias, one he called 'pernicious', later known as Addisonian anaemia. The other he associated now with bronzed skin and suprarenal pathology, true Addison's disease. Publication produced no fanfares, no royal honours and his fame has been mainly posthumous. In any case, he was too late for our first famous patient with Addison's disease, who was that model of sense and sensibility, Jane Austin.
Like its houses, its chairs and its coffee pots, 18th century England has managed to convey to us a society which was at once both sensible and elegant. It seemed to manifest good manners, piety, and cultivated discernment.


At least it did if you were of 'the gentry', which was the case with Jane Austen, one of the greatest writers in the English language. It was a lifestyle which provided the ideal ambience in which her genius could flourish.


Daughter of a clergyman, the seventh of eight children, she led a life of gentility and ease spent entirely in the quieter rural southern England. She drew her characters from her own circle and never strayed from the world in which she moved.


Further, she was much too well bred to let her own name grace the title-page of her novels. All her books were styled as being written, 'By a Lady', as indeed they were.


Her towering reputation is based on only six works of fiction written between the ages of 34 until her death at 41. They have never been out of print in 175 years, and have flourished even more during the last decade or so.


She never married, and it appears the creative impulse, then customarily fulfilled by the task of being a wife and mother, was in her attained through her art. She took considerable pains to conceal from her friends and visitors the nature of her life's work, and wrote on small pieces of paper, the more easily to slip under a blotter or into a drawer if chanced upon. She said her books were her children and she was later remembered as the caring wit of the family.


Jane Austen was born 20 years before Addison, in 1775, into a closely-knit family in which she led a sheltered home life, interspersed with occasional visits to Bath to take the waters, or to the nearby houses of her elder brothers.


It all sounds like a rural idyll, and so it was, until June 1816, when at the age of 40, she had an attack of nausea and vomiting and low backache.


In July she was depressed and felt weak. This was put down to her dissatisfaction with the book, 'Persuasion', which she had just completed. Two months later it was noted she tired easily, had uncharacteristic mood swings and further back pains. She improved and life progressed in its customary premeditated way.
In December she declined an invitation to dinner, saying 'The walk is beyond my strength, though I am otherwise very well.'


The following months she wrote to a friend that she was stronger but felt 'bile' was at the bottom of her nausea and malaise.


All pretty vague so far. Then in March 1817 Jane wrote to her favourite niece, Fanny, and in it gave the clue which could lead us to the likely diagnosis. She wrote, 'I certainly have not been very well for many weeks; I have a good deal of fever at times, but am considerably better now and recovering my looks a little, which have been black and white and every wrong colour. Sickness is a dangerous indulgence at my time of life.'


She wrote to a friend two months later, recounting details of recurrent vomiting, concluding, 'My chief sufferings were from feverish nights, weakness and languor.'


We know the slightly built Austen was bright eyed and had an olive complexion, certainly not 'black and white and every wrong colour.' A visitor in May observed the author was looking very pale and spoke in a weak, low voice.


A concerned family moved her to Winchester to be nearer expert medical help. It was of no avail. Over a six weeks period she became progressively weaker and had a number of fainting fits, until on July 18th, 1817, after several hours of unconsciousness, Jane Austen died in the arms of her only sister, Cassandra.
So what did she have? Well I don't think she died of boredom, as someone unkindly suggested. The story is one of unimpaired intellect but increasing languor and intermittent backache, fainting attacks, gastrointestinal disturbances, and fever, especially at night. Night sweats are a well-known feature of tuberculosis. Added to all that, and crucially, is a darkening of the face. The delicacy of the era regrettably precludes us from knowing about skin changes elsewhere, especially the vagina, in the mouth or where pressure was applied to the skin, at the waist, for instance.


A number of conditions come to mind, but probably only one fits the whole scenario.


The lassitude could have been due to a rare neuromuscular condition, myasthenia gravis, but there seems to have been no speech or swallowing problems. Maybe the heart could be implicated with an infection of its valves, or bacterial endocarditis, but fainting crises are not a feature of this. Perhaps cancer of the stomach with anaemia from the slight but persistent blood loss which characterises the condition. The digestive problems did not seem either very great or progressive.


Skin discolouration occurs in a number of general diseases: the rare so-called bronzed diabetes, or haemochromatosis, but the other symptoms do not fit; chronic inorganic arsenic poisoning with its raindrop pigmentation and abdominal symptoms, or indeed poisoning from any of the heavy metals, lead especially, possibly from medication or water pipes. But the other history is inappropriate and no other family member was affected.


No, none of these seem right. From the admittedly rather thin records, coupled with the melancholy fact that living in the country she did have ready access to almost certainly tubercular contaminated milk, the most likely diagnosis is Addison's disease due to TB of the hormone producing suprarenal glands.


As we have seen, it was not until 1849 that Thomas Addison first described the malady. It's best known features are weakness and skin discolouration which he described as 'various tints of deep amber or chestnut brown.'


One alleged feature was not displayed. My old forthright chief used to claim, rightly or wrongly, that tubercular patients, possibly due to their low grade persistent fever, were almost always more sexually charged than the general run of the population. No hint of sexual impropriety in Miss Austen has come down to us.


Whatever her private life, we know from her books that Jane Austen was a consummate writer whose genius was tempered with gentle humour and a subtle insight into the nature of humankind. It is better we remember her thus, rather than someone who suffered from an uncommon and debilitating medical disorder.


Until the mid-20th century, tuberculosis was the prime cause of Addison's disease. Now it is likely to be an auto immune reaction, as was believed to be the case in that other famous sufferer and quite different personality, John F. Kennedy.


I have spoken before in this place about Kennedy, so will not burden you with the details again. But briefly, during the 1960 Presidential campaign, a Republican questioned the candidate about an article in the November 1955 edition of the American Medical Association's Archives of Surgery, and which was concerned with operating for one reason or other, on sufferers from Addison's disease. The questioner wondered if JFK was one of these cases.


The piece was entitled 'Management of Adrenocortical Insufficiency During Surgery'. Of the three listed cases, one told of an unnamed man in for a bone fusion, and insertion of a metal plate who had had Addison's for seven years, and who was managed by desoxycorticosterone pellets every three months and 25 milligrams of cortisone daily by mouth.


It was a typical bread and butter piece for that journal, but suddenly became hot political property when at the end of the piece the authors inserted a quite unnecessary throwaway line which sparked off the question. They simply wrote, 'The operation was accomplished on October 21st, 1954.'


Now on October 11th, on page 39 of The New York Times, it was reported that 37-year-old Senator Kennedy was entering hospital for spinal surgery. On the 21st it wrote he had undergone the operation that day. On February 26th 1955 it saw fit to record that the plate had been removed.


Now you don't need much nous to conclude that two people of the same age, with the same spinal condition, having undergone similar surgery in the same hospital and who returned on exactly the same day four months later to have the plate removed, were in fact one and the same. So we know for certain John Kennedy had Addison's.


His treatment was successful, but in those days, dosage of cortisone was chancy. Accumulating drug gave a fullness of the face, a so-called moon face, which in the President gave him those boyish good looks and appearance of rude good health which made him the darling of the chattering classes.


It increased energy and JFK's well-known bedroom athleticism may have been enhanced by the treatment, though his back will have suffered.


Kennedy did not die of the disease, Jane Austen did. Treatment was relatively unrefined in one and non-existent in the other. The basic cause in one was probably tuberculosis; in the other, an auto immune reaction. The victims had widely differing personalities, but both had one thing in common, and something which indeed they shared with Thomas Addison: they touched the lives of countless people in all corners of the globe and have gone on doing so long after their deaths.


Robyn Williams: Jim Leavesley, in forensic mood, as always. His book is called 'What Killed Jane Austen, and Other Medical Mysteries', published by Harper Collins.
Next week, Sue Taylor has trouble with elephants. I'm Robyn Williams.
Guests on this program:

Dr. James Leavesley
Margaret River
Western Australia
Author of the book: "What killed Jane Austen and other Medical Mysteries", published by Harper & Collins