Publications by authors named "Drenthen J"

Background And Purpose: Various electrodiagnostic criteria have been developed in Guillain-Barré syndrome (GBS). Their performance in a broad representation of GBS patients has not been evaluated. Motor conduction data from the International GBS Outcome Study (IGOS) cohort were used to compare two widely used criterion sets and relate these to diagnostic amyotrophic lateral sclerosis criteria.

View Article and Find Full Text PDF

Background: Current diagnostic methods for nerve compression headaches consist of diagnostic nerve blocks. A less-invasive method that can possibly aid in the diagnosis is ultrasound, by measuring the cross-sectional area (CSA) of the affected nerve. However, this technique has not been validated, and articles evaluating CSA measurements in the asymptomatic population are missing in the current literature.

View Article and Find Full Text PDF

Background And Objectives: Chronic axonal polyneuropathy is a common disease of the peripheral nervous system with increasing prevalence with age. Typical neurologic signs are present in patients with polyneuropathy but may also occur in individuals without disease. Owing to limited knowledge on normal aging of the peripheral nervous system, it can be difficult to distinguish peripheral nerve dysfunction due to disease from variations in normal aging.

View Article and Find Full Text PDF
Article Synopsis
  • Chronic axonal polyneuropathy is becoming more common with age and significantly impacts daily life, but many individuals do not seek medical help, leading to underreporting of its prevalence.
  • A study conducted from 2013 to 2020 in the Netherlands included over 4,000 participants and found that the age-standardized prevalence of the condition was about 3% in Europe and the U.S., and projected to increase by 25% in the next 20 years.
  • Many participants had undiagnosed polyneuropathy, with notable risk factors including diabetes and vitamin deficiencies, and over 20% of cases exhibited multiple risk factors.
View Article and Find Full Text PDF

Electrodiagnostic (EDx) studies are helpful in diagnosing and subtyping of Guillain-Barré syndrome (GBS). Published criteria for differentiation into GBS subtypes focus on cutoff values, but other items receive less attention, although they may influence EDx subtyping: (a) extensiveness of EDx testing, (b) nerve-specific considerations, (c) distal compound muscle action potential (CMAP)-amplitude requirements, (d) criteria for conduction block and temporal dispersion. The aims of this study were to investigate how these aspects were approached by neuromuscular EDx experts in practice and how this was done in previously published EDx criteria for GBS.

View Article and Find Full Text PDF
Article Synopsis
  • - The study explores how genetic factors related to diabetes, body mass index (BMI), vitamin B12 levels, and alcohol intake may be linked to chronic axonal polyneuropathy, a common nerve disease, using data from the Rotterdam Study involving 1,565 participants.
  • - Findings reveal that higher polygenic scores (PGSs) for diabetes, BMI, and alcohol intake correlate with a greater prevalence of polyneuropathy, while higher PGSs for vitamin B12 levels are linked to a lower prevalence.
  • - The results suggest a potential causal relationship between these clinical risk factors and polyneuropathy, reinforcing the need for further research on genetic influences in this condition.
View Article and Find Full Text PDF

Objective: To describe the heterogeneity of electrodiagnostic (EDx) studies in Guillain-Barré syndrome (GBS) patients collected as part of the International GBS Outcome Study (IGOS).

Methods: Prospectively collected clinical and EDx data were available in 957 IGOS patients from 115 centers. Only the first EDx study was included in the current analysis.

View Article and Find Full Text PDF

Half of the world's population is at risk of arthropod-borne virus (arbovirus) infections. Several arbovirus infections have been associated with Guillain-Barré syndrome (GBS). We investigated whether arboviruses are driving GBS beyond epidemic phases of transmission and studied the antibody response to glycolipids.

View Article and Find Full Text PDF

Objective: While integrity of spinal pathways below injury is generally thought to be an important factor in the success-rate of neuromodulation strategies for spinal cord injury (SCI), it is still unclear how the integrity of these pathways conveying the effects of stimulation should be assessed. In one of our institutional case series of five patients receiving dorsal root ganglion (DRG)-stimulation for elicitation of immediate motor response in motor complete SCI, only two out of five patients presented as responders, showing immediate muscle activation upon DRG-stimulation. The current study focuses on post hoc clinical-neurophysiological tests performed within this patient series to illustrate their use for prediction of spinal pathway integrity, and presumably, responder-status.

View Article and Find Full Text PDF

Background: Treatment with one standard dose (2 g/kg) of intravenous immunoglobulin is insufficient in a proportion of patients with severe Guillain-Barré syndrome. Worldwide, around 25% of patients severely affected with the syndrome are given a second intravenous immunoglobulin dose (SID), although it has not been proven effective. We aimed to investigate whether a SID is effective in patients with Guillain-Barré syndrome with a predicted poor outcome.

View Article and Find Full Text PDF

Background And Purpose: The aim of this study was to determine the frequency of over- and underdiagnosis of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and to identify related diagnostic pitfalls.

Methods: We conducted a retrospective study in Dutch patients referred to the Erasmus University Medical Centre Rotterdam between 2011 and 2017 with either a diagnosis of CIDP or another diagnosis that was revised to CIDP. We used the European Federation of Neurological Societies/Peripheral Nerve Society (EFNS/PNS) 2010 diagnostic criteria for CIDP to classify patients into three groups: overdiagnosis, underdiagnosis, or confirmed diagnosis of CIDP.

View Article and Find Full Text PDF

Background And Purpose: Chronic axonal polyneuropathy is a common, usually multifactorial, disease for which there is no treatment yet available. We investigated the association between cardiovascular health, defined by the health score of the American Heart Association, and chronic axonal polyneuropathy.

Methods: Between June 2013 and January 2017, we investigated participants of the Rotterdam Study, a population-based cohort study.

View Article and Find Full Text PDF
Article Synopsis
  • Guillain-Barré syndrome (GBS) has two main subtypes: acute inflammatory demyelinating polyneuropathy (AIDP) and acute motor axonal neuropathy (AMAN), with early nerve excitability changes being key indicators of subtype.
  • A study involving 19 patients from The Netherlands and 22 from Bangladesh used compound muscle action potential (CMAP) scans within days of weakness onset to assess nerve function.
  • Results showed distinct CMAP scan patterns between AMAN and AIDP patients, particularly in stimulus intensity, suggesting that early CMAP scans can help identify GBS subtype early on.
View Article and Find Full Text PDF

Objectives: Current strategies for motor recovery after spinal cord injury (SCI) aim to facilitate motor performance through modulation of afferent input to the spinal cord using epidural electrical stimulation (EES). The dorsal root ganglion (DRG) itself, the first relay station of these afferent inputs, has not yet been targeted for this purpose. The current study aimed to determine whether DRG stimulation can facilitate clinically relevant motor response in motor complete SCI.

View Article and Find Full Text PDF
Article Synopsis
  • The study aimed to explore the link between diet quality and chronic axonal polyneuropathy among 1650 participants with an average age of 69.1 years.
  • Researchers used food frequency questionnaires and various medical evaluations to assess diet quality and the presence of polyneuropathy.
  • Results indicated no overall association between diet quality and polyneuropathy, but a notable finding suggested that salt intake of ≤6 g/day may be connected to a lower risk of this condition.
View Article and Find Full Text PDF

Objective: To study excitability of single motor units (MUs) using high-density surface-EMG.

Methods: Motor unit action potentials (MUAPs) were evoked by submaximal stimulation of the median nerve at the wrist and recorded with a 9 × 14 electrode grid on the skin overlying the thenar muscles. For excitability tests of single MUs, the most optimal specific single-channel surface-EMG signal was selected based on the spatiotemporal profile of single MUs.

View Article and Find Full Text PDF

Mycoplasma pneumoniae (Mp) triggers Guillain-Barré syndrome (GBS) and elicits anti-galactocerebroside (GalC) antibodies. Specifically anti-GalC IgG is associated with Mp-GBS, possibly because of its better ability to cross the blood-nerve barrier (BNB). We here investigated CSF for the presence of anti-GalC in GBS.

View Article and Find Full Text PDF

Objective: To extensively investigate the association of chronic polyneuropathy with basic and instrumental activities of daily living (BADL and IADL), falls, and gait.

Methods: A total of 1,445 participants of the population-based Rotterdam Study (mean age 71 years, 54% women) underwent a polyneuropathy screening involving a symptom questionnaire, neurologic examination, and nerve conduction studies. Screening yielded 4 groups: no, possible, probable, and definite polyneuropathy.

View Article and Find Full Text PDF

Residual motor nerve dysfunction after pediatric Guillain-Barré syndrome (GBS) was determined in an observational cross-sectional cohort study in patients who previously developed GBS during childhood (<18 years). Ulnar motor nerve dysfunction was defined by compound motor action potential (CMAP) scan in patients after a follow up of at least 1 year compared with age-matched healthy controls, in relation to clinical course and outcome. A total of 37 persons previously diagnosed with GBS in childhood were included with a mean age at current examination of 20.

View Article and Find Full Text PDF

Polyneuropathy is a prevalent and disabling disorder. Despite extensive evaluation, the cause often remains unknown. Factors that predispose for the development of polyneuropathy need to be identified.

View Article and Find Full Text PDF

To describe the key diagnostic features of pediatric Guillain-Barré syndrome (GBS) and validate the Brighton criteria. Retrospective cohort study of all children (<18 years) diagnosed with GBS between 1987 and 2013 at Sophia Children's Hospital, Erasmus MC, Rotterdam. Clinical information was collected and the sensitivity of the Brighton criteria was calculated.

View Article and Find Full Text PDF

Objective: To determine the prevalence of chronic polyneuropathy in an unselected community-dwelling population of middle-aged and elderly people.

Methods: The current study was embedded in the prospective, population-based Rotterdam Study. Between June 2013 and October 2015, 1,310 participants (mean age 70 years, 55% female) were screened for the presence of polyneuropathy.

View Article and Find Full Text PDF