Article
Psychiatry
Kenneth S. Kendler, Astrid Klee
Summary: In 1916, Ernst Rudin published a groundbreaking study on psychiatric genetics, which examined the inheritance patterns of dementia praecox in families. He found that the risk of siblings developing the disorder was lower than expected for a recessive disorder, and discussed alternative genetic models. Furthermore, Rudin established that dementia praecox was genetically related to other non-DP psychotic disorders. It is important to note that Rudin supported Nazi eugenic policies later in his career.
SCHIZOPHRENIA BULLETIN
(2022)
Article
Psychiatry
Kenneth S. Kendler
Summary: In 1921, at the age of 65, Emil Kraepelin concluded his long career by defining the essential features of dementia praecox, acknowledging the possibility of remissions and recovery. He emphasized the frequency of bizarre delusions and passivity symptoms in his clinical descriptions, outlining 6 subtypes of DP. Kraepelin's original concept of DP was not immutable and expanded to include new concepts like simple DP, showing his openness to change and new ideas in psychiatry.
SCHIZOPHRENIA BULLETIN
(2021)
Article
Neurosciences
Aurelie P. Bussy, Jake P. Levy, Tristin Best, Raihaan Patel, Lani Cupo, Tim Van Langenhove, Jorgen E. Nielsen, Yolande Pijnenburg, Maria Landqvist M. Waldo, Anne M. L. Remes, Matthias L. Schroeter, Isabel Santana, Florence Pasquier, Markus Otto, Adrian Danek, Johannes Levin, Isabelle Le Ber, Rik Vandenberghe, Matthis Synofzik, Fermin Moreno, Alexandre de Mendonca, Raquel Sanchez-Valle, Robert Laforce, Tobias Langheinrich, Alexander Gerhard, Caroline R. Graff, Chris R. Butler, Sandro Sorbi, Lize Jiskoot, Harro C. Seelaar, John C. van Swieten, Elizabeth Finger, Maria Carmela Tartaglia, Mario Masellis, Pietro Tiraboschi, Daniela Galimberti, Barbara B. Borroni, James B. Rowe, Martina D. Bocchetta, Jonathan D. A. Rohrer, Gabriel A. Devenyi, M. Mallar Chakravarty, Simon Ducharme
Summary: Recent studies have shown that early cerebellar and subcortical changes are seen in the progression of genetic frontotemporal dementia due to specific gene mutations. This study aimed to investigate the relationship between cerebellar and subcortical atrophy and neuropsychiatric symptoms across different genetic mutations in FTD.
HUMAN BRAIN MAPPING
(2023)
Review
Genetics & Heredity
Kenneth S. Kendler, Virginia Justis
Summary: This article discusses Boven's MD thesis published in 1915, in which he examined pedigrees of patients with dementia praecox and manic-depressive insanity. Boven concluded that both disorders were hereditary, with manic-depressive insanity being directly transmitted within families and dementia praecox being more common in collateral relatives. He also found that the inheritance of these disorders did not follow Mendelian transmission. This study represents one of the first investigations of the familial relationship between these disorders using modern methods.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
(2023)
Article
Clinical Neurology
David D. Ward, Lindsay M. K. Wallace, Kenneth Rockwood
Summary: The study found that even after cognitive impairment, MCI patients with high frailty have a significantly increased risk of dementia, with a higher risk in the non-amnestic MCI group.
ANNALS OF NEUROLOGY
(2021)
Article
Clinical Neurology
Emma Louise Anderson, Neil M. Davies, Roxanna Korologou-Linden, Mika Kivimaki
Summary: This essay introduces Mendelian randomisation as an alternative approach to study risk factors for Alzheimer's disease and related dementias. However, unexpected findings have emerged when applying this method. Five potential explanations are considered in this essay, along with recommendations to enhance causal inference.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
(2023)
Article
Neurosciences
Helena Pelin, Marcus Ising, Frederike Stein, Susanne Meinert, Tina Meller, Katharina Brosch, Nils R. Winter, Axel Krug, Ramona Leenings, Hannah Lemke, Igor Nenadic, Stefanie Heilmann-Heimbach, Andreas J. Forstner, Markus M. Noethen, Nils Opel, Jonathan Repple, Julia Pfarr, Kai Ringwald, Simon Schmitt, Katharina Thiel, Lena Waltemate, Alexandra Winter, Fabian Streit, Stephanie Witt, Marcella Rietschel, Udo Dannlowski, Tilo Kircher, Tim Hahn, Bertram Mueller-Myhsok, Till F. M. Andlauer
Summary: Psychiatric disorders display diverse symptoms and progression patterns, with the current classification system failing to accurately represent their molecular causes and symptomatic variations. By utilizing high-dimensional data clustering, we identified five clusters of psychiatric patients with shared clinical and genetic characteristics, aiding in the understanding of the heterogeneity of psychiatric disorders and potentially facilitating personalized treatment approaches.
NEUROPSYCHOPHARMACOLOGY
(2021)
Article
Clinical Neurology
Peter S. Myers, Joshua J. Jackson, Amber K. Clover, Christina N. Lessov-Schlaggar, Erin R. Foster, Baijayanta Maiti, Joel S. Perlmutter, Meghan C. Campbell
Summary: Parkinson disease clinical subtypes show clear and temporally distinct patterns of symptom progression, particularly in cognitive and psychiatric features. Comprehensive clinical examinations are crucial as the order of symptom presentation impacts clinical prognosis.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
(2021)
Article
Multidisciplinary Sciences
Tobias Lindig, Benjamin Bender, Eva Buerkle, Vinod Kumar, Ulrike Ernemann, Ludger Schoels, Tim W. Rattay
Summary: This study tested the usability of automated data analysis in patients with hereditary spastic paraplegia type 4 (SPG4). The results showed that quantitative imaging reports can serve as easily accessible and fully automatic screening tools for clinicians, providing information about brain regions affected by the disease.
SCIENTIFIC REPORTS
(2022)
Article
Behavioral Sciences
Danielle Pearce, Rebecca L. Gould, Matthew Roughley, Gemma Reynolds, Emma Ward, Rohan Bhome, Suzanne Reeves
Summary: This study aimed to explore the neurobiological and neuropsychological correlates of paranoid and misidentification subtypes of psychosis in dementia, finding that the misidentification subtype showed greater cognitive deficits and accelerated decline, as well as more pronounced brain volume loss in multiple regions.
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
(2022)
Article
Clinical Neurology
Maura Malpetti, Timothy Rittman, Peter Simon Jones, Thomas Edmund Cope, Luca Passamonti, William Richard Bevan-Jones, Karalyn Patterson, Tim D. Fryer, Young T. Hong, Franklin Aigbirhio, John Tiernan O'Brien, James Benedict Rowe
Summary: In patients with familial frontotemporal dementia, neuroinflammation and abnormal protein aggregation were observed, with consistent tau distribution in MAPT mutations and heterogeneous distributions in carriers of GRN and C9orf72 mutations. This suggests that neuroinflammation plays a significant role in the pathophysiology of familial FTD.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
(2021)
Article
Clinical Neurology
Kiran Samra, Amy Macdougall, Georgia Peakman, Arabella Bouzigues, Martina Bocchetta, David M. Cash, Caroline Greaves, Rhian S. Convery, John C. van Swieten, Lize C. Jiskoot, Harro Seelaar, Fermin Moreno, Raquel Sanchez-Valle, Robert Laforce, Caroline Graff, Mario Masellis, Maria Carmela Tartaglia, James B. Rowe, Barbara Borroni, Elizabeth Finger, Matthis Synofzik, Daniela Galimberti, Rik Vandenberghe, Alexandre de Mendonca, Christopher R. Butler, Alexander Gerhard, Simon Ducharme, Isabelle Le Ber, Pietro Tiraboschi, Isabel Santana, Florence Pasquier, Johannes Levin, Markus Otto, Sandro Sorbi, Jonathan D. Rohrer, Lucy L. Russell
Summary: A study on frontotemporal dementia found that neuropsychiatric symptoms occur in mutation carriers at all disease stages, with hallucinations and delusions providing additional staging benefit. The inclusion of these features in rating scales could improve the evaluation of disease progression.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
(2023)
Article
Clinical Neurology
Giulia Grande, Alessandra Marengoni, Davide L. Vetrano, Albert Roso-Llorach, Debora Rizzuto, Alberto Zucchelli, Chengxuan Qiu, Laura Fratiglioni, Amaia Calderon-Larranaga
Summary: Older adults with neuropsychiatric, cardiovascular, and sensory impairment/cancer multimorbidity are at increased risk of dementia, with high CRP levels and APOEε4 carriers further elevating the risk. Identifying these high-risk groups could lead to tailored interventions for dementia prevention.
ALZHEIMERS & DEMENTIA
(2021)
Article
Clinical Neurology
Lina Zapata-Restrepo, Juan Rivas, Carlos Miranda, Bruce L. Miller, Agustin Ibanez, Isabel E. Allen, Katherine Possin
Summary: This study retrospectively reviewed medical records of 28 patients diagnosed with probable bvFTD in a public psychiatric hospital in Cali, Colombia. The majority of patients were initially misdiagnosed with a primary psychiatric condition, with a gender difference in psychiatric diagnosis but not in neuropsychiatric symptoms. These results emphasize the importance of improving bvFTD diagnosis in under-represented populations.
FRONTIERS IN NEUROLOGY
(2021)
Review
Genetics & Heredity
Kenneth S. Kendler, Astrid Klee
Summary: A new approach to psychiatric genetics research emerged in Germany from three roots: wide-spread acceptance of Kraepelin's diagnostic system, increasing interest in pedigree research, and excitement about Mendelian models. Two relevant papers from 1912 and 1913 were reviewed, analyzing pedigrees and focusing on the segregation of dementia praecox (DP) and manic-depressive insanity (MDI). While one author found the disorders to co-occur frequently, the other found them to be largely independent. They also examined other disorders or traits appearing in the pedigrees.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
(2023)