Open-access Searching for neurological diseases in the Julio-Claudian dynasty of the Roman Empire

À procura de doenças neurológicas na dinastia Júlio-Claudiana do Império Romano

ABSTRACT

The gens Julia was one of the oldest families in ancient Rome, whose members reached the highest positions of power. They made history because Julius Caesar, perpetual dictator, great-uncle of the first emperor, Augustus, passed his name on to the Julio-Claudian dynasty with the emperors Tiberius, Caligula, Claudius and Nero. Descriptions of the diseases of these emperors and some of his family members may indicate diagnoses such as epilepsy, dystonia, dementia, encephalitis, neurosyphilis, peripheral neuropathies, dyslexia, migraine and sleep disorders. In the historical context of ancient Rome, the possibility of infectious diseases related to the libertine way of life is quite large. However, there is a possibility that some of these diseases occurred from genetic transmission.

nervous system diseases; neurology; historical article; history of medicine

RESUMO

A gens Iulia era uma das mais antigas famílias da Roma Antiga, com membros que chegaram aos mais altos cargos. Ficaram na história por causa de Julius Caesar, ditador perpétuo, pai adotivo do primeiro imperador Augustus, por meio de quem seu nome passou para a dinastia Julio-Claudian com os imperadores Tiberius, Caligula, Claudius e Nero. Descrições de doenças desses imperadores e de alguns de seus familiares podem nos remeter a diagnósticos como epilepsia, distonia, demência, encefalites, neurossífilis, neuropatias periféricas, dislexia, migrânea e distúrbios do sono. No contexto histórico da Roma antiga, a possibilidade de doenças infecciosas e relacionadas ao modo de vida libertino é bastante grande. Entretanto, existe a possibilidade de que algumas dessas doenças tenham ocorrido por transmissão genética.

doenças do sistema nervoso; neurologia; artigo histórico; história da medicina

The gens Julia (the Julii) was one of the oldest families in ancient Rome, with members who reached the highest positions of power during the first years of the Republic (Figure 1). They made history because of Julius Caesar, perpetual dictator, great-uncle and foster father of the first emperor, Augustus, through whom the name was passed to the Julio-Claudian dynasty in the first century A.D., which included the emperors Tiberius, Caligula, Claudius and Nero (Figures 1 and 2)1.

Figure 1
Pedigree of the Julio-Claudian dynasty1,2,3,4.

Figure 2
Emperors of the Julio-Claudian dynasty.

Some of the dramatic moments of the lives of the emperors of this family are described, mainly by Suetonius2,3 and Plutarch4 (Table), as well as some of the attempts by their physicians to save them, or even to confirm one death, as did Antistius with Caesar.

Table
Assumptions for the neurological problems of Julio-Claudian family members1,2,3,4.

Julius Caesar

Julius Caesar (Figure 3) was not an emperor. He was granted the title of dictator, but a possible neurological problem may have prevented him from receiving the crown. His explanation for not attending the coronation was that “his senses do not remain steady’’ and he was ‘’speedily shaken and whirled about’’, resulting in ‘’giddiness’’ and “insensibility”3. The description may represent a focal epileptic seizure with alterations of perception4. Shakespeare’s5 version of this fact is much more dramatic (Chart).

Figure 3
Julius Caesar.

Chart
Julius Caesar by Shakespeare: epileptic seizure in the Senate5.

Caesar had frequent headaches, and two other epileptic seizures occurred when he was young. The first was in Cordoba (Hispania); the second when he was near Thapsus, at the moment when he was arranging his army into battle formation. As soon as he felt the first symptoms, without giving the disease time to overtake him and dull his already-affected senses, he made himself move to one of the towers on the outskirts and rested3. These descriptions are insufficient to claim generalized seizures, but there was certainly a focal seizure with alteration of perception4.

The cases of epilepsy in the family opens up speculation about the possibility of sudden unexplained death in epilepsy for the sudden deaths of Caesar’s father and grandfather, but there is no proof. It is possible that Caesariun, Caesar and Cleopatra’s son, had his first epileptic seizure at three years of age4.

Augustus

Augustus, Caesar’s great-nephew and heir, may have had depressive episodes during his life. It is reported that, in the course of a battle, after being defeated, Publius Varus immolated himself on his sword. Augustus’ reaction was merely apathy and to let his hair and beard grow1.

With respect to spelling, Augustus’ opinion was that one should write as one speaks. He used to invert or transpose not only letters, but also syllables. His grandson, Agrippa Postumus, also had a learning disorder2.

Augustus would wake up three to four times a night and, when some duty woke him early, he slept while being led through the streets, or when his litter stopped for a while2. This daytime sleepiness may have been the result of a sleep disorder. However, considering the possibility that his sister Octavia, and other members of the clan, suffered from epilepsy, it has been hypothesized that this sleepiness could have represented some kind of epileptic seizure4.

Perpetually suffering from headaches and vomiting, he suffered his whole life from many other dangerous and serious diseases, especially after the submission of Cantabria2. Clinical signals of fever with chills and intense sweating, associated with pain in the whole body and mental confusion with delirium dominated him for several weeks2. From these signs, whose etiology is not known, it is possible to make hypotheses about encephalitis, neurological features of sepsis, or even malaria. A statue of his doctor, Antonius Musa, was erected, on the feet of Aesculapius, for having cured him of these diseases1,2.

After an illness at a young age, Augustus developed a weak hip, thigh and left leg, and walked with a limping gait. His right-hand index finger was so weak that cold weather made it numb and contracted it, and he was able to write only by using a ring of horn2. There is no information to determine if it these were symptoms of peripheral neuropathies or sequelae of encephalitis or other diseases that he could have had during his life.

Tiberius

Augustus’ adoptive son, Tiberius’ left hand was stronger and more skillful than the right one. When he walked, he kept his neck rigid and tilted backwards, with a certain melancholy air, and was almost always silent. He spoke slowly, with a particular repetitive gesture with his fingers. Aside from this, he was in excellent health, and did not like help and advice from doctors; he would rather consult astrology2. His neck seems to have had a dystonia, retrocollis or torticollis, which may have been accompanied by dystonia of the right upper limb, as well as dystonia and/or hand chorea. The speech problem may have been a dysarthria or a dystonia of the larynx. One could also consider a parkinsonism associated with the movements of the hands, the melancholic air and slow speech6.

For his last 11 years, Tiberius lived on the island of Capri, indulging his carnal desires. He returned twice to the continent, but did not want to go to Rome for fear of meeting people. He died at 78 years of age, disturbed by macabre hallucinations, and trying to conceal his state under a mask of artificial joy. He shifted between this agitated state with alteration periods and loss of consciousness1.

As he was an alcoholic and lived in depravity and on an uncontrolled diet, it is possible to consider causes such as Wernicke’s encephalopathy, or a vascular disorder or syphilis as an etiology for dementia. The depressive symptoms, with movement disorders resulting in hallucinations and a “mask of artificial joy” may suggest a dementia with parkinsonism, as found in dementia with Lewy bodies7.

Caligula

Caligula, great-nephew and heir of Tiberius, was a victim of epileptic seizures from childhood. In his youth, he could not endure hardship without being affected by sudden fainting spells that required much sacrifice to enable him to walk, keep upright, take a deep breath and sustain himself. He was tortured by insomnia, as he did not sleep more than three hours per night2.

When Caligula came into power, he wanted to erase the painful memories of the sad reign of Tiberius1. However, after seven months in power, Caligula became seriously ill1,2. After recovering, the people from Rome found a much worse version of Caligula1. He tortured and murdered senators and Roman citizens, closed the stores and declared famine in the Empire; he wished for plagues, epidemics and earthquakes to arise, collected unfair high taxes, and wanted to govern, not only as a god, but as a super-god: Oderint dum metuant (let them hate, as long as they fear)1. At one feast, he was attacked abruptly by a crisis of intense laughter2.

Although it is possible that Caligula had syphilis8, the symptoms seem to compare more with an encephalitis, with a behavioral disorder from temporal lobe epilepsy. The clinical signs may have aggravated the epileptic seizures that he had since childhood4. A herpetic encephalitis may also be a possible etiology for the event9.

Claudius

Throughout almost all his childhood and adolescence, Caligula’s nephew and Julius Caesar’s great-great grandnephew, Claudius, suffered from various long-term diseases, which weakened him in such a way that he was considered unfit for any public function2. Antonia, his mother, stated that he was nothing but an “abortion that nature had begun to form, but never ended”1,2.

Claudius’ clinical signs were more prominent in adulthood, with changes of gait (clumsy walking and stumbling), continuous head shaking with alterations of movements and hypertrophy of the cervical muscles, involuntary movements of the limbs and face, that got worse with minimum effort and when he presented himself in public, as well as having well-delineated muscles of the body, dysarthria and dysphonia1,2. This description seems to point to a generalized dystonia and its peculiar characteristics, with the onset at the transition of childhood to adolescence. Remembering Tiberius’ clinical signs of a possible segmental dystonia, with cervical spine predominance, as well as dysphonia, one could postulate the possibility of a dystonia type DYT6, with reduced penetrance, in this family6.

Claudius’ son, Britannicus, the fruit of his relationship with his cousin Messalina, had epileptic seizures, probably a generalized primary epilepsy, between six and 13 years of age2,4,10.

Nero

Despite his life of orgies, Nero, Augustus’ great great grandson and adopted son of Claudius, had only been seriously ill about three times during his reign. Nero had a fetid odor; his body was covered in pustules and suspicious skin spots. His nape was thick and the belly prominent. Thin legs supported a heavy torso1.

The first five years of Nero’s reign were the five most joyful experienced by Rome. However, Nero became tyrannical, and developed delirious pretensions of being an artist, poet, actor, musician and religious worshiper. In the last years of his life he lost all sense of right and wrong. He isolated himself, and had countless wishes to kill himself. At age 32, in an advanced state of dementia, he stabbed a dagger into his throat1,2.

Nero’s described skin changes may be seen in patients with severe cases of syphilis, typically associated with malnutrition and alcohol consumption leading to a decrease in immunity9. The neurological signs are also compatible with neurosyphilis, which begins insidiously with behavioral disorders and cognitive signs such as irritability, inattention, emotional lability and delirium. It evolves into dementia, tremors, dysarthria, and epileptic seizures until there is motor loss with fecal and urinary incontinence8.

FINAL CONSIDERATIONS

Despite there being few reports, it is possible to make a series of hypotheses about the neurological diseases that affected the Julio-Claudian dynasty. The possibility of symptoms of infection as the etiology is quite prominent in the historical context. However, the consanguineous marriages, and the characteristics of dystonia and the epilepsies, may open the possibility of a discussion of genetic diseases in the emperors and their families.

References

  • 1 Lissner, I. Os Césares: apogeu e loucura. Belo Horizonte: Itatiaia; 1985.
  • 2 Suetônio. A vida dos doze Césares. São Paulo: Martin Claret; 2004. (Coleção A obra prima de cada autor. Série Ouro).
  • 3 Plutarco. Vidas paralelas: Alexandre e César. Porto Alegre: L± 2005
  • 4 Hughes JR. Dictator Perpetuus: Julius Caesar: did he have seizures? If so, what was the etiology? Epilepsy Behav. 2004:5(5);756-64. https://doi.org/10.1016/j.yebeh.2004.05.006
    » https://doi.org/10.1016/j.yebeh.2004.05.006
  • 5 Shakespeare W. Julius Caesar. New York: Washington Square; 1958.
  • 6 Camargo CH, Camargos ST, Cardoso FE, Teive HA. The genetics of the dystonias--a review based on the new classification of the dystonias. Arq Neuropsiquiatr. 2015;73(4):350-8. https://doi.org/10.1590/0004-282X20150030
    » https://doi.org/10.1590/0004-282X20150030
  • 7 Gomperts SN. Lewy body dementias: dementia with Lewy Bodies and Parkinson disease dementia. Continuum (Minneap Minn). 2016;22(2 Dementia):435-63. https://doi.org/10.1212/CON.0000000000000309
    » https://doi.org/10.1212/CON.0000000000000309
  • 8 Conde-Sendín MA, Hernández-Fleta JL, Cárdenes-Santana MA, Amela-Peris R. Neurosyphilis: forms of presentation and clinical management. Rev Neurol. 2002;35(4):380-6. Spanish.
  • 9 Li JH, Guo H, Zheng S, Li B, Gao XH, Chen HD. Widespread crusted skin ulcerations in a man with type II diabetes: a quiz. Acta Derm Venereol. 2015;95(5):632-3. https://doi.org/10.2340/00015555-1999
    » https://doi.org/10.2340/00015555-1999
  • 10 Michael BD, Solomon T. Seizures and encephalitis: clinical features, management, and potential pathophysiologic mechanisms. Epilepsia. 2012;53 Suppl 4:63-71. https://doi.org/10.1111/j.1528-1167.2012.03615.x
    » https://doi.org/10.1111/j.1528-1167.2012.03615.x

Publication Dates

  • Publication in this collection
    Jan 2018

History

  • Received
    29 Aug 2017
  • Reviewed
    29 Sept 2017
  • Accepted
    17 Oct 2017
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