Long-Term Outcome in Patients With Transient Global Amnesia: A Population-Based Study (2024)

Abstract

Transient global amnesia (TGA) is characterized by the sudden onset of anterograde amnesia, generally lasting up to 24 hours.^1-4 It has an annual incidence of 3.4 to 10.4 per 100,000 people.^5-7

The leading hypothesis on the pathogenesis of TGA is abnormal venous drainage of the temporal lobes caused by increased intrathoracic pressure resulting in jugular hypertension.^8-11 Others include arterial ischemia,¹² migraine-,^5,13,14 and epilepsy-related.¹⁵

The recurrence rate of TGA has been estimated to be between 2.9% and 23.8%.^13,16-19 Available studies about the long-term outcome are few and limited in scope. Acquiring information is necessary to enhance clinical practice.

Available data suggest that TGA does not put patients at a higher risk of cerebrovascular events, myocardial infarction, or peripheral artery disease.^13,16,19,20 Data on the risk of seizures after TGA are inconsistent. Studies that have suggested a higher risk of seizures concluded that at least some of the patients could have had a seizure mimicking TGA, as suggested by abnormal interictal electroencephalograms (EEGs).^5,11

The long-term risk of cognitive decline has not been sufficiently evaluated. Complete recovery of cognitive function has been reported 5 days to 6 months after the episode.^21-24 Other investigators have found memory and visuoperceptual dysfunction.^25-30 Long-term risk was assessed in one study with an average follow-up of 82.2 months, showing no difference in the incidence of dementia (2.9%) compared with general population.¹⁶

We conducted a population-based, matched cohort study on patients with TGA to establish the long-term risk of cerebrovascular events, seizures, and cognitive impairment.

Patients and Methods

A list of all patients with a potential diagnosis of TGA among residents of Olmsted County, Minnesota, occurring from January 1, 1985, through December 31, 2010, was obtained using the resources of the Rochester Epidemiology Project³¹ database. The list included patients diagnosed in both the outpatient and inpatient settings, including cases seen at Mayo Clinic, and those seen at other medical providers in Olmsted County. We reviewed electronic and paper medical records for all patients. TGA was defined clinically, and all cases were confirmed using previously proposed criteria.^1,32,33 Cases in which an alternative diagnosis was suspected or could not be ruled out were excluded from the study. Fourteen patients were excluded because of a confirmed diagnosis of seizures or stroke. The other 75 patients were excluded for suspicion of alternative diagnosis, including the classical differential diagnosis of TGA such as transient ischemic attack [TIA], seizures, and transient epileptic amnesia, with the latter consisting of focal seizures with similar clinical features, shorter duration and higher recurrence, and sometimes accompanied by other manifestations such as oral automatisms. One age- and sex-matched control for each case was selected from the same database; controls were also matched for date of assessment.

Data collected in both cases and controls included demographic characteristics, relevant cerebrovascular risk factors, and conditions reported to be associated with TGA (hypertension, dyslipidemia, diabetes mellitus, smoking history, coronary artery disease, atrial fibrillation, peripheral vascular disease, alcohol abuse, personal or familial history of stroke, personal or familial history of migraine, personal or familial history of seizures or epilepsy).

The primary end points for our analysis were cerebrovascular events (TIA or stroke), seizures, and cognitive impairment (diagnosis of mild cognitive impairment and dementia). The diagnosis of stroke or TIA was made on the basis of comprehensive data from the medical record, and using the definition on current guidelines.^34,35 The presence of seizures was recorded according to the clinical diagnosis by the treating neurologist, sometimes aided by an abnormal ictal or interictal EEG. The presence of cognitive impairment was considered to be the first time the patient was given a clinical diagnosis of mild cognitive impairment or dementia by a neurologist.^36,37 Secondary end points were death, functional outcome at last follow-up as assessed by the modified Rankin score (mRS)³⁸, and TGA recurrence.

Approval from the Ethics Standards Committee was obtained to conduct this retrospective study.

Results

Two hundred twenty-one cases and the same number of matched controls were included in the study (Figure 1). Baseline data for cases and controls are presented in the Table.

Among the patients with TGA, 20 (9.0%) had experienced 1 or more previous episodes of TGA. Twelve (5.4%) patients had recurrences after the index episode; 10 had only 1 recurrence and 2 had 4 recurrences each. The median interval to the first recurrence was 4.2 years (IQR, 2.8-8.4 years). The resulting recurrence rate from the index event was 67 per 100 person-years of follow-up (95% CI, 52.3-84.5).

The mean ± SD age at onset of TGA was 65.6±12.2 years (range, 0.07-29.93 years). A total of 111 (50.2%) patients were women. Data on TGA attack duration were available in 107 patients. They lasted from 0.16 to 36 hours, with a mean ± SD of 5.5±5.6 hours.

Potential precipitating factors for the episode were identified in 62 (28.0%) patients; 53 (24.0%) of them involved exercise, sexual intercourse, or a potential Valsalva-like maneuver such as coughing/choking or vomiting; 6 (2.7%) episodes occurred after exposure to heat while showering, and 3 (1.4%) after emotional stress.

A total of 172 (77.8%) patients underwent a computed tomography scan of the head as part of their workup. None of them was suggestive of an alternative diagnosis. Magnetic resonance imaging was performed in 47 of the 221 (21.27%) patients included in the study. Only 2 (4.26%) of them showed the classically described punctate hyperintensity on diffusion weighted imaging in the hippocampal region. No other abnormalities were found on magnetic resonance imaging. The EEG was done in 72 (32.6%) patients, including 11 on the same day of the episode; the rest of the patients had the EEG within a median of 4 days (IQR, 2-13 days) after the TGA episode had resolved. Of 11 EEGs performed on the day of the episode, only 1 was abnormal, showing temporal lobe slowing. Among the other 61 EEGs, 6 (9.8%) showed temporal slowing. No epileptiform discharges or seizures were noted.

The prevalence of cerebrovascular risk factors and conditions associated with TGA was compared between patients with TGA and controls (Table). No significant differences were found in the frequency of hypertension, dyslipidemia, history of coronary artery disease, atrial fibrillation, peripheral vascular disease, smoking history, or personal or familial history of stroke or seizures. Body mass index was not different between the 2 groups. Diabetes mellitus had a higher prevalence among controls (P=.033). History of migraine was the only baseline factor that was more frequent among TGA cases (42 [19.1%] vs 12 [5.4%]; P<.001). However, family history of migraine was not different between the 2 groups.

The mean follow-up period in subjects with TGA was 12±7 years, with a median mRS of 0 (IQR, 0-0; range, 0-6) at last follow-up. In controls, the length of follow-up was 12.3 ± 7 years and median mRS at last follow-up was 0 (IQR, 0-0; range, 0-5). During follow-up, there were 142 deaths in the TGA group and 127 among controls (P=.34). Median time to death was similar between the TGA group and the control group (22.5 vs 17.1 years; log-rank P=.34).

There were no statistically significant differences between survival curves for the TGA group and the control group using time to any type of cerebrovascular event (log-rank P=.30), time to seizures event (log-rank P=.55), and time to cognitive impair event (log-rank P=.88) as end points (Figure 2). No particular dementia etiology (degenerative or vascular) predominated in one group over the other. In the TGA group, there was also no evidence of an association between TGA recurrence and cognitive impairment (P=77), cerebrovascular event (P=71), or seizures (P=46). Median time to death was similar between the TGA group and the control group (21.7 vs 17.1; log-rank P=34).

Discussion

In this case cohort, population-based study, we examined the risk of cerebrovascular events, seizures, and cognitive impairment after a single episode or multiple episodes of TGA. Our results demonstrate that patients are not at a higher risk of having a cerebrovascular event, seizures, or developing cognitive impairment over the long-term after an episode of TGA. The population-based, casematched design and long length of follow-up of our study strongly support the validity of our results. Previous reports suggested that the incidence of cerebrovascular events after an episode of TGA does not differ from that in the general population, though these previous studies typically had shorter follow-up and therefore could not be as conclusive.^13,16,19,20 In addition, our results provide further argument against the hypothesis that arterial ischemia could be the pathophysiological mechanism of TGA, not only because of the lack of association with subsequent stroke/TIA but also because there were no differences in baseline cardiovascular risk factors between cases of patients with TGA and controls. Instead, the finding that exercise or a Valsalva maneuver was the most common precipitating factor suggests that venous hypertension might be responsible for the symptoms.^8-11

Our study found that the risk of seizures after an episode of TGA is not increased and previous seizures are not a risk factor for TGA. These findings argue against an epileptic mechanism for TGA. Of note, focal seizures can present with manifestations resembling TGA. These patients diagnosed with transient amnesia associated with epilepsy have a different disease (ie, epilepsy) and were consequently not included in our cohort. Epilepsy initially masquerading as TGA may explain the cases of epilepsy diagnosed after an episode of TGA in previous smaller studies.^5,19

Our study found that having 1 or more episodes of TGA does not impact the risk of developing subsequent cognitive impairment. This conclusion is reassuring and clinically important because previous studies evaluating the long-term risk of cognitive impairment in patients with TGA had produced variable results.^21-30 However, only 1 of those studies had a relatively long follow-up (∼6 years).¹⁶ We did not find a higher incidence of cognitive impairment in the TGA group over a mean follow-up of 12 years, even among those patients with recurrent TGA. We cannot confirm nor refute whether preexisting structural abnormalities in the limbic system might precipitate an episode of TGA as has been previously postulated,³⁹ but our results suggest that recurrent episodes of TGA would not represent a structural disruption in connectivity of memory pathways given that the long-term incidence of cognitive impairment is not increased. This is also supported by previous imaging studies that have shown no evidence of structural brain injury after TGA.⁴⁰

We found a rate of recurrence of 5.4% in our patients with TGA. This rate is lower than in most previous studies.^13,16-20 This difference may be related to the strict criteria we used for the diagnosis of TGA (ie, careful exclusion of patients with possible alternative diagnoses).

The association between migraine and TGA has been previously reported^5,13,14 and was confirmed in our analysis. This association between the 2 conditions and their occasional familial aggregation may suggest a possible genetic predisposition, which needs to be investigated in future research. It is difficult to rule out, however, that a higher prevalence of migraine could be consistently found among patients with TGA due to the bias introduced by treating clinicians specifically enquiring about it, knowing their proposed association.

The population-based design and length of follow-up longer than a decade make our study unique. Although the possibility of selection bias had been a consistent limitation in most previous literature on TGA, this bias is much less likely in our population-based cohort. Meanwhile, the length of follow-up in our study was markedly longer than in any previous study on TGA, thus supporting the reliability of our findings.

We acknowledge that missing information is always a possibility with any retrospective data collection; yet, this is unlikely given the comprehensive nature of our medical records and the fact that we had full access to all the medical information from the 2 centers where our patients could have received local medical care. The workup of patients varied according to the preference of the treating physician, but we do not think that such variability compromises the validity of our main results.

Conclusion

We conclude that having 1 or more episodes of TGA does not increase the long-term risk of cerebrovascular events, seizures, or cognitive impairment, compared with general population. This is very valuable reassuring information for the counseling of patients with TGA and their families. The previously reported association between TGA and migraine was confirmed in our study. Further research is warranted to determine the origin of such association.

Acknowledgments

Grant Support: This study was made possible by the Rochester Epidemiology Project (grant number R01-AG034676; Principal Investigator: Walter A. Rocca, MD, MPH, and Jennifer L. St Sauver, PhD).

Abbreviations and Acronyms

References