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Published on: November 9, 2017
Guillain-Barré syndrome following primary cytomegalovirus infection: a prospective cohort study
David Orlikowski1, Raphaël Porcher, Valérie Sivadon-Tardy
1Service de Réanimation, AP-HP, Hôpital Raymond Poincaré, Garches, France.
Insights
Cytomegalovirus (CMV) infection can cause Guillain-Barré syndrome (GBS), with similar risks to Campylobacter jejuni infection. Factors like older age and ventilation impact long-term outcomes in CMV-GBS patients.
Area of Science:
- Neurology
- Infectious Diseases
- Epidemiology
Background:
- Epidemiology and prognostic factors of cytomegalovirus (CMV) infection-associated Guillain-Barré syndrome (GBS) are poorly understood.
- Cytomegalovirus (CMV) is a common virus with potential neurological complications.
Purpose of the Study:
- To investigate the epidemiology of Guillain-Barré syndrome (GBS) following primary cytomegalovirus (CMV) infection.
- To identify prognostic factors associated with CMV-GBS and long-term neurological sequelae.
Main Methods:
- Prospective follow-up of 506 GBS patients from 1996-2006.
- Diagnosis of 63 CMV-GBS cases using IgM and IgG avidity tests; plasma CMV DNA detection.
- Statistical analysis including Fisher's exact test, Wilcoxon rank-sum test, and time series analysis.
Main Results:
- CMV-GBS predominantly affected young adults but included a subgroup of women over 50.
- Sensory defects (72%) and facial palsy (49%) were common; CMV DNA in plasma correlated with sensory defects.
- Long-term neurological sequelae (21%) were linked to older age and mechanical ventilation.
- CMV-GBS cases showed a decreasing trend (1996-2006) and seasonal periodicity (July-October).
- Estimated incidence of CMV-GBS was 0.6-2.2 per 1000 primary CMV infections.
Conclusions:
- The risk of GBS following primary CMV infection is comparable to that of Campylobacter jejuni infection.
- Findings suggest viral replication plays a role in the neuropathology of CMV-GBS.
- This study enhances understanding of CMV-GBS epidemiology and clinical characteristics.
Background:
Little is known about the epidemiology and the prognostic factors of Guillain-Barré syndrome (GBS) following primary infection with cytomegalovirus (CMV-GBS).
Methods:
We prospectively followed up 506 patients with cases of GBS who were admitted to our center from 1996 through 2006. We diagnosed 63 (12.4%) CMV-GBS cases by immunoglobulin (Ig) M detection and IgG avidity. Plasma CMV DNA was detected at hospital admission. Patient subgroups were compared using Fisher's exact test and the Wilcoxon rank-sum test. Temporal variations were analyzed with time series methods.
Results:
Patients with CMV-GBS were mostly young (median age, 32 years; sex ratio, 0.85), but we also identified a subpopulation of patients consisting of women aged >50 years. Sensory defects (in 72% of cases) and facial palsy (49%) were frequent, and test results positive for CMV DNA in plasma at hospital admission (found in 62% of cases) tended to be associated with objective sensory defect (P=.052). The main factors associated with long-term neurological sequelae (21%) were older age (P<.001) and assisted ventilation during hospitalization (P=.005). The number of CMV-GBS cases decreased between 1996 and 2006 (P=.019) and displayed an annual periodicity between the months of July and October. The incidence of CMV-GBS was estimated to be between 0.6 and 2.2 cases per 1000 cases of primary CMV infection (versus 0.25 to 0.65 cases per 1000 cases of Campylobacter jejuni infection).
Conclusions:
This study provides new insights about the epidemiology of CMV-GBS and shows that the risk of developing GBS is similar following primary CMV infection or C. jejuni infection. Our results also suggest a direct or indirect involvement of viral replication in the neuropathological processes of CMV-GBS.
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