#Peer-reviewed #Journal

Vasta R, Callegaro S, Grassano M, Canosa A, Cabras S, Di Pede F, Matteoni E, De Mattei F, Casale F, Salamone P, Mazzini L, De Marchi F, Moglia C, Calvo A, Chiò A, Manera U

In this paper, we evaluate the effect of exposure to electromagnetic fields on ALS onset age and progression rate. We studied the association of patients’ residency with the distribution of power lines and repeater antennas. We did not find any significant relationship between electromagnetic fields and ALS phenotype or progression.

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#Peer-reviewed #Journal

Chio A, Moglia C, Canosa A, Manera U, Grassano M, Vasta R, Palumbo F, Gallone S, Brunetti M, Barberis M, De Marchi F, Dalgard C, Chia R, Mora G, Iazzolino B, Peotta L, Traynor B, Corrado L, D’Alfonso S, Mazzini L, Calvo A

ATXN2 is a gene related to a neurodegenerative disease called Spinocerebellar Ataxia type 2, but it is also a recognised risk factor for ALS. In this study, we explored the role of the so-called intermediate repeated expansion (a specific type of mutations characterised by the wrong repetition of short sequences of DNA that produces altered amminoacidic sequences called polyQ) in the determination of ALS patients’ phenotype. We discovered that patients with these alterations showed an early age at onset and a higher progression rate. We confirmed that ATXN2 can be a potential target for new therapeutic approaches.

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#Peer-reviewed #Journal

Grassano M, Calvo A, Moglia C, Sbaiz L, Brunetti M, Barberis M, Casale F, Manera U, Vasta R, Canosa A, D’Alfonso S, Corrado L, Mazzini L, Dalgard C, Karra R, Chia R, Traynor B, Chiò A

ALS is probably caused by an interplay between environmental and genetic factors. Several descriptions of patients carrying more than one pathogenic mutation are present in scientific literature, but few papers systematically evaluated the presence of mutations in ALS-related genes in population-based cohorts. In this study, we highlighted that the presence of more than one mutation is more common than expected. Patients with more than one mutation resulted to have more aggressive phenotypes, confirming that disease  features can be due to the malfunction of several neuronal pathways.

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#Peer-reviewed #Journal

Palumbo F, Iazzolino B, Peotta L, Canosa A, Manera U, Grassano M, Casale F, Pellegrino G, Rizzone MG, Vasta R, Moglia C, Chiò A, Calvo A

ALS is mainly a neurodegenerative disease involving motor system, but also some aspects of cognition can be impaired. Social cognition is one of the most important brain function in humans, being responsible for our social living and well-being. We prospectively studied a cohort of ALS patients belonging to Piedmont ALS registry using neuropsychological tests specifically designed for assess social cognition. ALS patients showed significant lower scores than healthy controls, confirming a social cognition deficit than needs to be taken into account in patients management.

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#Peer-reviewed #Journal

Susana Pinto, Marta Gromicho, Miguel Oliveira Oliveira Santos, Michael Swash & Mamede De Carvalho

This study focused on persons with a rare type of ALS known as respiratory onset ALS. This type of ALS begins with breathing problems and affects the diaphragm muscle, which is essential for respiration.
The study discovered that most persons with respiratory onset ALS are elderly men who are underweight. They must begin utilizing non-invasive ventilation (NIV), which helps them breathe, earlier than patients with other types of ALS.
Despite NIV therapy, persons with respiratory onset ALS have a worse life expectancy than those with other types of ALS. The study also found that the pattern of how ALS spreads throughout the body does not affect how quickly people need NIV or how long they live.

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#Peer-reviewed #Journal

Santos Silva C, Gromicho M, Oliveira Santos M, Pinto S, Swash M, de Carvalho

This study looked into whether thyroid dysfunction or an imbalance in the hormones produced by the thyroid gland, is linked to amyotrophic lateral sclerosis (ALS).
The researchers compared the prevalence of thyroid dysfunction in ALS patients to that of people with non-thyroid-related neuromuscular disorders. They discovered that ALS patients had a lower prevalence of thyroid dysfunction than the control group, indicating that thyroid dysfunction is not a major contributor to ALS development.
The researchers also reviewed previous studies on thyroid dysfunction and ALS and discovered that their findings were consistent with those of other studies.
Overall, this study suggests that thyroid dysfunction does not pose a significant risk for ALS.

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Miguel Oliveira Santos, Marta Gromicho, Susana Pinto, Michael Swash, Mamede de Carvalho

Swallowing problems, or dysphagia, are a common symptom of ALS. People with ALS who are on continuous non-invasive ventilation (NIV), a breathing treatment, frequently develop dysphagia.
Doctors often debate whether or not to insert a feeding tube called a gastrostomy in ALS patients who use NIV. A gastrostomy is a surgical procedure that delivers food directly to the stomach via a tube.
This study examined patients with ALS who were already using NIV and investigated whether mild dysphagia affected their survival. The researchers analyzed the data from these patients and discovered that mild dysphagia did not affect their survival.
This study is important because it provides information that helps doctors make decisions about gastrostomy in patients with ALS who use NIV. The findings suggest that mild dysphagia is not a major factor in survival for these patients.

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#Peer-reviewed #Journal

Diogo F. Soares, Rui Henriques, Marta Gromicho, Mamede de Carvalho, Sara C. Madeira

This research introduces a new type of understandable models for predicting how diseases progress over time, focusing on a specific group of patients with certain characteristics. We developed a new method called TCtriCluster, which looks for meaningful patterns in data collected over time from these patients, helping us understand the progression of the disease better. By using these patterns, we improved the accuracy of predicting important events in ALS, such as when patients might need breathing assistance or other types of support. This method performed better than existing ones, with high accuracy in predicting when certain interventions might be needed. This approach was tested on a large group of ALS patients in Portugal, providing valuable insights for healthcare professionals in managing the disease and its various stages.

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#Peer-reviewed #Journal

Marta Gromicho, Miguel Oliveira Oliveira Santos, Susana Pinto, Michael Swash & Mamede De Carvalho

This research paper looked at a specific type of ALS called flail arm syndrome (FAS). FAS is characterized by weakness in the upper limbs, and it typically progresses slowly. The researchers studied the clinical features, progression, and survival of FAS patients, and they found that the presence or absence of upper motor neuron (UMN) signs at diagnosis was the most important factor in determining how long a patient would live.
The researchers found that the location of the weakness, whether it was in the distal muscles of the arms (the muscles closest to the fingers) or the proximal muscles of the arms (the muscles closest to the shoulders), did not affect the prognosis of FAS patients. This suggests that the most important factor in determining the prognosis of FAS is the severity of the disease, as indicated by the presence or absence of UMN signs.

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#Peer-reviewed #Journal

Catarina Falcão de Campos, Marta Gromicho, Hilmi Uysal, Julian Grosskreutz, Magdalena Kuzma-Kozakiewicz, Miguel Oliveira Santos, Susana Pinto, Susanne Petri, Michael Swash and Mamede de Carvalho

This paper investigated how long it takes to diagnose amyotrophic lateral sclerosis (ALS). The researchers examined data from more than 1,400 ALS patients from four different countries and discovered that the median diagnostic delay was 11 months. This means that it took people an average of 11 months from the time they noticed symptoms to being officially diagnosed with ALS.
The researchers discovered that several factors contributed to the diagnostic delay, including:
Symptom presentation: In the early stages of ALS, symptoms are frequently mild and nonspecific, making diagnosis difficult.
Referral to specialists: Many people with ALS are not initially referred to a neurologist, who is the specialist who can make a definitive diagnosis of ALS.
Testing: Electromyography (EMG) is a test that is used to measure electrical activity in muscles. EMG is very important for diagnosing ALS, but it is not always available or accessible.
The researchers propose that a specific diagnostic test for ALS, such as a biomarker, could help to shorten the diagnostic time. They also emphasize the importance of referring patients to a neurologist and performing an EMG to diagnose ALS early on.

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#Peer-reviewed #Journal

Miguel Oliveira Santos, Marta Gromicho, Ana Pronto-Laborinho and Mamede de Carvalho

This research paper explores the possible connection between amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease that affects muscle control, and myopathy, a muscular condition that weakens muscles. The researchers describe three cases of ALS patients who also had myopathy, suggesting that there may be a link between these two conditions and that they may share some common causes.

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Susana Pinto, Miguel Oliveira Santos, Marta Gromicho, Michael Swash, Mamede de Carvalho

This research paper examined the association between respiratory symptoms and respiratory test results in patients with amyotrophic lateral sclerosis (ALS). The researchers found that there are three distinct groups of ALS patients based on their respiratory symptoms and test results. Patients with the most severe respiratory problems were more likely to need mechanical ventilation. Measuring the phrenic nerve amplitude may be helpful in identifying patients who are at risk of developing severe respiratory problems. Orthopnea is a severe symptom that should prompt NIV and early NIV promotes survival.

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Miguel Oliveira Santos, Marta Gromicho, Susana Pinto, Ana Pronto-Laborinho and Mamede de Carvalho

This research paper explores the characteristics of patients with amyotrophic lateral sclerosis (ALS) who originate from Sub-Saharan Africa (SSA) and are diagnosed and followed in a specialized ALS clinic in Portugal. Sub-Saharan African Amyotrophic Lateral Sclerosis (SAALS) is a distinct population with a younger onset age and a longer disease duration, but total survival is independent of SA ancestry. The researchers believe that the specialized ALS clinic in Portugal, with its access to respiratory care and riluzole, could explain the observed differences between their results and previous data from African ALS patients followed in their own countries. Improving access to healthcare for SAALS patients could help to improve their survival rates.

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#Peer-reviewed #Journal

Inês Alves, Marta Gromicho, Miguel Oliveira Oliveira Santos, Susana Pinto, Ana Pronto-Laborinho, Michael Swash & Mamede De Carvalho

This research paper investigated the clinical and demographic characteristics of motor neuron disease (MND) patients over a 27-year period. The researchers found that the average age at onset of MND was increasing, diagnostic delay was decreasing, and the proportion of patients using respiratory support with noninvasive ventilation (NIV) was increasing. They also found that median survival was increasing for ALS patients with spinal onset.

The researchers suggest that these changes are likely due to improved comprehensive care for MND patients. They believe that early diagnosis and treatment, including the use of NIV, are contributing to the better outcomes seen in recent years.

The researchers’ findings are important for future studies exploring the impact of new treatments on MND patients.

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#Peer-reviewed #Journal

Chio A, Moglia C, Canosa A, Manera U, Grassano M, Vasta R, Palumbo F, Gallone S, Brunetti M, Barberis M, De Marchi F, Dalgard C, Chia R, Mora G, Iazzolino B, Peotta L, Traynor BJ, Corrado L, Dalfonso S, Mazzini L, Calvo A.

In this paper we analysed, in a huge cohort of ALS patients belonging to the Piemonte and Valle d’Aosta registry, the copresence of pathogenic variants (a permanent change in the DNA sequence) in ALS related genes. We discovered that the 54% of patients carried at least one detrimental common variant or repeat expansion and the identification of the interactive effects of modifier genes represents a crucial clue for explaining ALS clinical heterogeneity. Gene variants act as modifiers of ALS survival and can act on their own or in unison.

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#Peer-reviewed #Journal​

Manera U, Grassano M, Matteoni E, Bombaci A, Vasta R, Palumbo F, Torrieri MC, Cugnasco P, Moglia C, Canosa A, Chiò A, Calvo A.

To early recognise respiratory failure signs in ALS patients is of outstanding importance to precocious treat it with non-invasive ventilation. Many tests can be used to evaluate respiratory function in early phases: no one of them is considered unfailing, so a combination of them is usually performed in clinical practice. We identified than serum chloride, measured by a simple venous blood sampling, can add useful information by identifying patients that are starting to compensate acidosis due to nocturnal hypoventilation and the consequent increase of blood carbon dioxide, by increasing blood carbonate and expelling chloride in urines. Serum chloride is a cheap and widely diffuse that should be added to the initial standard examination in ALS patients.

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Manera U, D’Ovidio F, Cabras S, Torrieri MC, Canosa A, Vasta R, Palumbo F, Grassano M, De Marchi F, Mazzini L, Mora G, Moglia C, Calvo A, Chiò A. 

ALS is one of the more heterogeneous neurological disease and the prediction of its progression is one of the most important topic in ALS research. Moreover, no study have previously evaluated the timing of progression in the different body regions that can be involved by the disease. To do that we collected a huge dataset comprehending all the ALS functional rating scale (ALSFRS-R) scores and, by performing different analysis, we discovered that functional impairment runs faster in the body regions involved later, suggesting a snowball-like behaviour of the disease.

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Miguel Oliveira Santos, Marta Gromicho, Susana Pinto, Michael Swash, Mamede de Carvalho

It is unknown if mild dysphagia affects survival of patients with amyotrophic lateral sclerosis (ALS) on continuous non-invasive ventilation (NIV). We often must discuss the pros and cons of gastrostomy in patients with NIV, but there is a lack of information on the issue. We, therefore, studied dysphagia as a survival predictor factor in patients with ALS already adapted to continuous NIV, using our collected data.
Our findings are relevant for decision-making processes concerning gastrostomy in this particular population.

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#Peer-reviewed #Journal

Cláudia Santos Silva, Miguel Oliveira Santos, Marta Gromicho, Ana Pronto-Laborinho, Isabel Conceição & Mamede de Carvalho

This research paper explores the potential link between transthyretin (TTR) gene mutations and motor neuron disease (MND). TTR is a protein that plays a crucial role in protecting nerve cells from damage. Mutations in the TTR gene can cause the protein to malfunction and form amyloid deposits, which can lead to nerve damage and a condition called amyloidosis.
The researchers studied three patients with MND who were also found to carry the pVal50Met mutation of the TTR gene. This mutation is associated with a rare form of amyloidosis called hereditary amyloid transthyretin (ATTRv) amyloidosis. The researchers examined the patients’ clinical symptoms, imaging scans, cerebrospinal fluid tests, nerve conduction studies, and small fiber tests.
The researchers’ findings suggest that he TTR gene mutations may contribute to the development of MND in some patients.

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Catarina Falcão de Campos, Marta Gromicho, Hilmi Uysal, Julian Grosskreutz, Magdalena Kuzma-Kozakiewicz, Miguel Oliveira Santos, Susana Pinto, Susanne Petri, Michael Swash, Mamede de Carvalho

This paper discusses the challenges of diagnosing amyotrophic lateral sclerosis (ALS). The researchers found that people with spinal onset ALS, slower disease progression, cognitive symptoms at onset, and lower income were more likely to experience delays in diagnosis.
The authors also identified the referral process from non-neurologists to neurologists as a potential factor contributing to these delays. They suggest that early referral to a neurologist could help to expedite the diagnosis and improve outcomes for ALS patients.

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