Transient global amnesia
Areas of hypoperfusion, seen above in the left sided hippocampus (seen as white punctate lesions on diffusion weighted MRI) are a characteristic finding in Transient Global Amnesia
SpecialtyNeurology
SymptomsMemory impairment
ComplicationsUsually no long term sequelae
Usual onsetSudden
DurationLess than 24 hours
CausesUnknown
Diagnostic methodClinical diagnosis, imaging may aid in diagnosis
TreatmentReassurance
MedicationNone
PrognosisGood

Transient global amnesia (TGA) is a neurological disorder whose key defining characteristic is a temporary but almost total disruption of short-term memory with a range of problems accessing older memories. A person in a state of TGA exhibits no other signs of impaired cognitive functioning but recalls only the last few moments of consciousness, as well as possibly a few deeply encoded facts of the individual's past, such as their childhood, family, or home perhaps.[1][2]

Both TGA and anterograde amnesia deal with disruptions of short-term memory. However, a TGA episode generally lasts no more than 2 to 8 hours before the patient returns to normal with the ability to form new memories.

Signs and symptoms

A person having an attack of TGA has almost no capacity to establish new memories, but generally appears otherwise mentally alert and lucid, possessing full knowledge of self-identity and identity of close family, and maintaining intact perceptual skills and a wide repertoire of complex learned behavior. The individual simply cannot recall anything that happened outside the last few minutes, while memory for more temporally distant events may or may not be largely intact.[1][2] The degree of amnesia is profound, and, in the interval during which the individual is aware of his or her condition, is often accompanied by anxiety.[3] The diagnostic criteria for TGA, as defined for purposes of clinical research, include:[2]

  • The attack was witnessed by a capable observer and reported as being a definite loss of recent memory (anterograde amnesia).
  • There was an absence of clouding of consciousness or other cognitive impairment other than amnesia.
  • There were no focal neurological signs or deficits during or after the attack.
  • There were no features of epilepsy, or active epilepsy in the past two years, and the patient did not have any recent head injury.
  • The attack resolved within 24 hours.

Progression of a TGA event

This onset of TGA is generally fairly rapid, and its duration varies but generally lasts between 2 and 8 hours.[2] A person experiencing TGA has memory impairment; with an inability to remember events or people from the past few minutes, hours or days (retrograde amnesia) and has working memory of only the past few minutes or less, thus they cannot retain new information or form new memories beyond that period of time (anterograde amnesia).[4] One of its bizarre features is perseveration, in which the victim of an attack faithfully and methodically repeats statements or questions, complete with profoundly identical intonation and gestures "as if a fragment of a sound track is being repeatedly rerun."[5] This is found in almost all TGA attacks and is sometimes considered a defining characteristic of the condition.[2][6][7] The individual experiencing TGA retains social skills and older significant memories, almost always including knowing his or her own identity and the identity of family members, and the ability to perform various complex learned tasks including driving and other learned behavior; one individual "was able to continue putting together the alternator of his car."[2] Also, during episodes of TGA, a person's personality remains intact and the episode is not associated with loss of consciousness, a decreased level of consciousness or cognitive deficits (other than memory impairment).[4] Though outwardly appearing to be normal, a person with TGA is disoriented in time and space, perhaps knowing neither the year nor where they reside. Although confusion is sometimes reported, others consider this an imprecise observation,[7] but an elevated emotional state (compared to patients experiencing Transient Ischemic Attack, or TIA) is common.[8] In a large survey, 11% of individuals in a TGA state were described as exhibiting "emotionalism" and 14% "fear of dying".[9] The attack lessens over a period of hours, with older memories returning first, and the repetitive fugue slowly lengthening so that the victim retains short-term memory for longer periods. This characteristic of TGA, where the length of time affected by retrograde amnesia shortens (i.e. older memories return first, followed by more recent memories) is commonly seen.[4] In the majority of cases there are no long-term effects other than a complete lack of recall for this period of the attack and an hour or two before its onset.[2][10] However, while seemingly back to normal within 24 hours, there are subtle effects on memory that may persist longer.[11][12] There is emerging evidence for observable impairments in a minority of cases weeks or even years following a TGA attack.[11][13][14]

Causes

The underlying cause of TGA remains enigmatic. The leading hypotheses are some form of epileptic event, a problem with blood circulation around, to or from the brain, or some kind of migraine-like phenomenon.[8][15][16][17] The differences are sufficiently meaningful that transient amnesia may be considered a heterogeneous clinical syndrome[2] with multiple etiologies, corresponding mechanisms, and differing prognoses.[9]

Precipitating events

TGA attacks are associated with some form of precipitating event in at least one-third of cases.[18] The most commonly cited precipitating events include vigorous exercise (including sexual intercourse), swimming in cold water or enduring other temperature changes, and emotionally traumatic or stressful events.[2] There are reports of TGA-like conditions following certain medical procedures and disease states.[16] One study reports two cases of familial incidence (in which two members of the same family experienced TGA), out of 114 cases considered.[2] This indicates the possibility that there could be a slight familial incidence.

If the definition of a precipitating event is widened to include events days or weeks earlier, and to take in emotionally stressful burdens such as money worries, attending a funeral or exhaustion due to overwork or unusual childcare responsibilities, a large majority, over 80%, of TGA attacks are said to correlate with precipitating events.[9]

The role of psychological co-factors has been addressed by some research. It is the case that people in a state of TGA exhibit measurably elevated levels of anxiety and/or depression.[3] Emotional instability may leave some people vulnerable to stressful triggers and thus be associated with TGA.[9] Individuals who have experienced TGA, compared with similar people with TIA, are more likely to have some kind of emotional problem (such as depression or phobias) in their personal or family history[19] or to have experienced some kind of phobic or emotionally challenging precipitating event.[20]

Vascular hypotheses

Cerebral ischemia is a frequently disputed possible cause, at least for some segment of the TGA population, and until the 1990s it was generally thought that TGA was a variant of transient ischemic attack (TIA) secondary to some form of cerebrovascular disease.[8][17] Those who argue against a vascular cause point to evidence that those experiencing TGA are no more likely than the general population to have subsequent cerebral vascular disease.[8] In fact, "in comparison with TIA patients, TGA patients had a significantly lower risk of combined stroke, myocardial infarct, and death."[19]

Other vascular origins remain a possibility, however, according to research of jugular vein valve insufficiency in patients with TGA. In these cases TGA has followed vigorous exertion. One current hypothesis is that TGA may be due to venous congestion of the brain,[21] leading to ischemia of structures involved with memory, such as the hippocampus.[22] It has been shown that performing a Valsalva maneuver (involving "bearing down" and increasing breath pressure against a closed glottis, which occurs frequently during exertion) may be related to retrograde flow of blood in the jugular vein, and therefore, presumably, cerebral blood circulation, in patients with TGA.[21][23][24][25][26]

Migraine

A history of migraine is a statistically significant risk factor for the development of TGA.[8][9][4] "When comparing TGA patients with normal control subjects… the only factor significantly associated with an increased risk for TGA was migraine."[17] Fourteen percent of people with TGA had a history of migraine in one study,[18] and approximately a third of the participants in another clinical study reported such a history.[2]

However, migraine does not appear to occur simultaneously with TGA nor serve as a precipitating event. Headache frequently occurs during TGA, as does nausea, both symptoms often associated with migraine, but it appears that these do not indicate migraine in patients during a TGA event. The connection remains conceptual, and muddied further by a lack of consensus about the definition of migraine itself, and by the differences in age, gender, and psychological characteristics of migraine sufferers when compared to those variables in the TGA cohort.[9]

Epilepsy

Amnesia is often a symptom in epilepsy, and for that reason people with known epilepsy are disqualified from most studies of TGA. In a study where strict criteria were applied to TGA diagnosis, no epileptic features were seen in EEGs of over 100 patients with TGA.[9] However, despite the fact that EEG readings are usually normal during a TGA attack, and other usual symptoms of epilepsy are not observed with TGA,[17] it has been speculated that some initial epileptic attacks present as TGA.[2] The observation that 7% of people who experience TGA will develop epilepsy calls into question whether those case are, in fact, TGA or transient epileptic amnesia (TEA).[8] TEA attacks tend to be short (under one hour) and tend to recur, so that a person who has experienced both repeated attacks of temporary amnesia resembling TGA and if those events lasted less than one hour is very likely to develop epilepsy.[2]

There is additional speculation that atypical cases of TEA in the form of nonconvulsive status epilepticus may present with duration similar to TGA.[27] This may constitute a distinct subgroup of TGA. TEA, as opposed to "pure" TGA, is also characterized by "two unusual forms of memory deficit …: (i) accelerated long-term forgetting (ALF): the excessively rapid loss of newly acquired memories over a period of days or weeks and (ii) remote autobiographical memory loss: a loss of memories for salient, personally experienced events of the past few decades."[6]

Whether an amnestic event is TGA or TEA thus presents a diagnostic challenge,[16] especially in light of the recently published descriptions of possible long-term cognitive deficits with (presumably correctly diagnosed) TGA.

Diagnosis

There is no universally accepted diagnostic criteria for TGA, however proposed diagnostic criteria include: the absence of seizures, the absence of a head injury, symptoms that resolve within 24 hours, and the dysfunction or impairment being limited to amnesia (both retrograde and anterograde).[4] TGA is a clinical diagnosis and brain imaging or other testing is not required for the diagnosis.[4] However, brain imaging is often obtained to rule out other serious causes of sudden amnesia, including a stroke. Brain imaging is usually normal during and immediately after an episode of TGA. However delayed diffusion weighted MRI (obtained 12–48 hours after the episode) can sometimes show punctate lesions in the hippocampus (one of the areas of the brain responsible for memory) or adjacent areas of the brain. These lesions are transient; often persisting for several days after the episode.[4]

Functional MRI may show bitemporal hypoperfusion during an episode of TGA. Other areas affected include the hippocampus, parahippocampal gyrus, and amygdala.[4]

Other than memory impairment, the neurological exam is usually normal and without focal deficits.[28]

Laboratory tests may be obtained to rule out other causes of sudden amnesia such as a complete blood count, electrolytes, kidney function, liver function, inflammatory markers (such as C reactive protein and erythrocyte sedimentation rate), ammonia level (often elevated in hepatic encephalopathy), urine toxicology screening, alcohol level and thyroid stimulating hormone level.[28]

Differential diagnosis

A differential diagnosis should include:[29]

If the event lasts less than one hour, transient epileptic amnesia (TEA) might be implicated.[2][30]

If the condition lasts longer than 24 hours, it is not considered TGA by definition. A diagnostic investigation would then probably focus on some form of undetected ischemic attack or cranial bleed.[31][32]

Prognosis

The prognosis of "pure" TGA is very good, as by definition, symptoms resolve within 24 hours. It does not affect mortality or morbidity[29] There is no treatment specific to TGA.[4] "The most important part of management after diagnosis is looking after the psychological needs of the patient and his or her relatives. Seeing a once competent and healthy partner, sibling or parent become incapable of remembering what was said only a minute ago is very distressing, and hence it is often the relatives who will require reassurance."[33]

It is unclear if episodes of TGA increase the future risk of a stroke. Some population based studies show no increased risk of a stroke after an episode of TGA, while other population based studies show a slightly increased risk.[34][35][4]

Recurrence rates of TGA are variously reported, with one systematic calculation suggesting the rate is under 6% per year.[19] Fifteen percent of people who have had an episode of TGA have multiple episodes, with an average interval of 2 years between episodes.[4]

TGA may have multiple etiologies and prognoses.[9] Atypical presentations may masquerade as epilepsy[8] and be more properly considered TEA. In addition to such probable TEA cases, some people experiencing amnestic events diverging from the diagnostic criteria articulated above may have a less benign prognosis than those with "pure" TGA.[2]

Recently, moreover, both imaging and neurocognitive testing studies question whether TGA is as benign as has been thought. MRI scans of the brain in one study showed that among people who had experienced TGA, all had cavities in the hippocampus, and these cavities were far more numerous, larger, and more suggestive of pathological damage than in either healthy controls or a large control group of people with tumor or stroke.[13] Verbal and cognitive impairments have been observed days after TGA attacks, of such severity that the researchers estimated the effects would be unlikely to resolve within a short time frame.[14] A large neurocognitive study of patients more than a year after their attack has shown persistent effects consistent with amnestic mild cognitive impairment (MCI-a) in a third of the people who had experienced TGA.[36] In another study, "selective cognitive dysfunctions after the clinical recovery" were observed, suggesting a prefrontal impairment.[12] These dysfunctions may not be in memory per se but in retrieval, in which speed of access is part of the problem among people who have had TGA and experience ongoing memory problems.[11]

Epidemiology

The estimated annual incidence of TGA varies from a minimum of 2.9 cases per 100,000 population (in Spain) and 5.2 per 100,000 (in the US),[29] but among people aged over 50, the rate of TGA incidence is reported to range from approximately 23 per 100,000 (in a US population) to 32 per 100,000 (in a population in Scandinavia).[18][37]

TGA is most common in people between age 56 and 75,[9] with the average age of a person experiencing TGA being approximately 62.[8]

See also

References

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  2. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Hodges; Warlow, CP (1990). "Syndromes of transient amnesia: towards a classification. A study of 153 cases". Journal of Neurology, Neurosurgery, and Psychiatry. 53 (10): 834–43. doi:10.1136/jnnp.53.10.834. PMC 488242. PMID 2266362.
  3. 1 2 Noel, A.; Quinette, P.; Guillery-Girard, B.; Dayan, J.; Piolino, P.; Marquis, S.; De La Sayette, V.; Viader, F.; et al. (2008). "Psychopathological factors, memory disorders and transient global amnesia". The British Journal of Psychiatry. 193 (2): 145–51. doi:10.1192/bjp.bp.107.045716. PMID 18670000.
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  12. 1 2 Le Pira; Giuffrida, S; Maci, T; Reggio, E; Zappalà, G; Perciavalle, V (2005). "Cognitive findings after transient global amnesia: role of prefrontal cortex". Applied Neuropsychology. 12 (4): 212–7. doi:10.1207/s15324826an1204_5. PMID 16422663. S2CID 12629136.
  13. 1 2 Nakada; Kwee, IL; Fujii, Y; Knight, RT (2005). "High-field, T2 reversed MRI of the hippocampus in transient global amnesia". Neurology. 64 (7): 1170–4. doi:10.1212/01.WNL.0000156158.48587.EA. PMID 15824342. S2CID 17306379.
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  15. ↑ Enzinger, C.; Thimary, F.; Kapeller, P.; Ropele, S.; Schmidt, R.; Ebner, F.; Fazekas, F. (2008). "Transient Global Amnesia: Diffusion-Weighted Imaging Lesions and Cerebrovascular Disease". Stroke. 39 (8): 2219–25. doi:10.1161/STROKEAHA.107.508655. PMID 18583561.
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  17. 1 2 3 4 Zorzon, Marino; Antonutti, L; Masè, G; Biasutti, E; Vitrani, B; Cazzato, G (1995). "Transient Global Amnesia and Transient Ischemic Attack : Natural History, Vascular Risk Factors, and Associated Conditions". Stroke. 26 (9): 1536–42. doi:10.1161/01.STR.26.9.1536. PMID 7660394.
  18. 1 2 3 Miller, J. W.; Petersen, R; Metter, E; Millikan, C; Yanagihara, T (1987). "Transient global amnesia: Clinical characteristics and prognosis". Neurology. 37 (5): 733–7. doi:10.1212/wnl.37.5.733. PMID 3574671. S2CID 44321336. Archived from the original on 2009-09-12. Retrieved 2009-10-07.
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  20. ↑ Inzitari; Pantoni, L; Lamassa, M; Pallanti, S; Pracucci, G; Marini, P (1997). "Emotional arousal and phobia in transient global amnesia". Archives of Neurology. 54 (7): 866–73. doi:10.1001/archneur.1997.00550190056015. PMID 9236576.
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  22. ↑ Chung, C. -P.; Hsu, HY; Chao, AC; Chang, FC; Sheng, WY; Hu, HH (2006). "Detection of intracranial venous reflux in patients of transient global amnesia". Neurology. 66 (12): 1873–7. doi:10.1212/01.wnl.0000219620.69618.9d. PMID 16801653. S2CID 39724390.
  23. ↑ Sander, Kerstin; Sander, Dirk (2005). "New insights into transient global amnesia: recent imaging and clinical findings". The Lancet Neurology. 4 (7): 437–44. doi:10.1016/S1474-4422(05)70121-6. PMID 15963447. S2CID 19997499.
  24. ↑ Moreno-lugris; Martínez-Alvarez, J; Brañas, F; Martínez-Vázquez, F; Cortés-Laiño, JA (1996). "Transient global amnesia. Case-control study of 24 cases". Revista de Neurología. 24 (129): 554–7. PMID 8681172.
  25. ↑ Nedelmann; Eicke, BM; Dieterich, M (2005). "Increased incidence of jugular valve insufficiency in patients with transient global amnesia". Journal of Neurology. 252 (12): 1482–6. doi:10.1007/s00415-005-0894-9. PMID 15999232. S2CID 25268484.
  26. ↑ Akkawi NM, Agosti C, Rozzini L, Anzola GP, Padovani A (2001). "Transient global amnesia and venous flow patterns". The Lancet. 357 (9256): 639. doi:10.1016/S0140-6736(05)71434-3. PMID 11558519. S2CID 5978618.
  27. ↑ Vuilleumier, P.; Despland, P; Regli, F (1996). "Failure to recall (but not to remember): Pure transient amnesia during nonconvulsive status epilepticus". Neurology. 46 (4): 1036–9. doi:10.1212/wnl.46.4.1036. PMID 8780086. S2CID 40835407. Archived from the original on 2005-11-14. Retrieved 2009-10-18.
  28. 1 2 Sealy, David; Tiller, Robert J.; Johnson, Katherine (January 2022). "Transient Global Amnesia". American Family Physician. 105 (1): 50–54. ISSN 1532-0650. PMID 35029951.
  29. 1 2 3 Sucholeiki, Roy (3 December 2008). "Transient Global Amnesia". eMedicine. Medscape. Retrieved 19 October 2009.
  30. ↑ Engmann, Birk; Reuter, Mike (2003). "A case history of sudden memory dysfunction – caused by transient epileptic amnesia". Aktuelle Neurologie. 30 (7): 350–353. doi:10.1055/s-2003-41889. S2CID 59264426.
  31. ↑ Landres B: UCLA Department of Medicine Clinical Vignette: Transient Global Amnesia. Last Revised: Sun, 13-Apr-2003. "UCLA Department of Medicine - wfsection-Transient Global Amnesia". Archived from the original on 2012-03-09. Retrieved 2012-07-03. accessed 9/26/09
  32. ↑ Monzani; Rovellini, A; Schinco, G; Silani, V (2000). "Transient global amnesia or subarachnoid haemorrhage? Clinical and laboratory findings in a particular type of acute global amnesia". European Journal of Emergency Medicine. 7 (4): 291–3. doi:10.1097/00063110-200012000-00007. PMID 11764138. S2CID 2450356.
  33. ↑ Magnus Harrison; Mark Williams (2007). "The diagnosis and management of transient global amnesia in the emergency department". Emerg Med J. 24 (6): 444–445. doi:10.1136/emj.2007.046565. PMC 2658295. PMID 17513554.
  34. ↑ Lee, Sang Hun; Kim, Keon-Yeup; Lee, Jeong-Woo; Park, So-Jeong; Jung, Jin-Man (1 April 2022). "Risk of ischaemic stroke in patients with transient global amnesia: a propensity-matched cohort study". Stroke and Vascular Neurology. 7 (2): 101–107. doi:10.1136/svn-2021-001006. ISSN 2059-8688. PMC 9067272. PMID 34702748.
  35. ↑ Mangla, Atul; Navi, Babak B.; Layton, Kelly; Kamel, Hooman (February 2014). "Transient Global Amnesia and the Risk of Ischemic Stroke". Stroke. 45 (2): 389–393. doi:10.1161/STROKEAHA.113.003916. PMC 3946840. PMID 24309586.
  36. ↑ Borroni; Agosti, C; Brambilla, C; Vergani, V; Cottini, E; Akkawi, N; Padovani, A (2004). "Is transient global amnesia a risk factor for amnestic mild cognitive impairment?". Journal of Neurology. 251 (9): 1125–7. doi:10.1007/s00415-004-0497-x. PMID 15372257. S2CID 20602707.
  37. ↑ Koski; Marttila, RJ (1990). "Transient global amnesia: incidence in an urban population". Acta Neurologica Scandinavica. 81 (4): 358–60. doi:10.1111/j.1600-0404.1990.tb01571.x. PMID 2360405. S2CID 32980858.
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