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Jeromin, Andreas

Mayo Clinic

Quanterix (United States)

Citations 9

Plasma neurofilament light chain predicts disease progression in asymptomatic genetic frontotemporal dementia (P5.1-007)
-Martinez, Julio Rojas, Wang, Ping , Staffaroni, Adam M. , Wolf, Amy , Heuer, Hilary W. , Taylor, Joanne, Jeromin, Andreas, Rosen, Howard J. , Boxer, Adam L. , Cobigo, Yann , Fong, Jamie , Boeve, Bradley F.

Neurology | December 7, 2023 | Volume: 92 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.92.15_supplement.p5.1-007 Get It

Comparison of Plasma Phosphorylated Tau Species With Amyloid and Tau Positron Emission Tomography, Neurodegeneration, Vascular Pathology, and Cognitive Outcomes
Frank, Ryan D. , Dage, Jeffrey L. , Jeromin, Andreas, Ashton, Nicholas J. , Blennow, Kaj , Karikari, Thomas K. , Vanmechelen, Eugeen , Lowe, Val J. , Bu, Guojun , Vemuri, Prashanthi , Graff‐Radford, Jonathan , Jack, Clifford R. , Petersen, Ronald C. , Jack, Clifford R , Vemuri, Prashanthi , Bu, Guojun , Ashton, Nicholas J , Dage, Jeffrey L , Mielke, Michelle M. , Karikari, Thomas K. , Zetterberg, Henrik , Algeciras‐Schimnich, Alicia , Knopman, David S.

JAMA Neurology | July 26, 2021 | Volume: 78 | Issue: 9 | Pages: 1108

10.1001/jamaneurol.2021.2293 Get It

Recommendations of the Global Multiple System Atrophy Research Roadmap Meeting
Walsh, Ryan R., Krismer, Florian , Galpern, Wendy R., Wenning, Gregor K. , Low, Phillip A. , Halliday, Glenda M. , Holton, Janice L. , Quinn, Niall , Rascol, Olivier , Shaw, Leslie M. , Eidelberg, David , Bower, Pam, Abler, Victor, Biedenharn, Judy, Bitan, Gal , Brundin, Patrik , Fernandez, Hubert, Fortier, Philip, Gasser, Thomas , Hewitt, Alice, Höglinger, Günter U. , Huentelman, Matt , Jensen, Poul Henning , Jeromin, Andreas, Kang, Un Jung , Kaufmann, Horacio , Kellerman, Lawrence R., Khurana, Vikram , Klockgether, Thomas , Kim, Woojin S. , Langer, Carol B., Masliah, Eliezer , Meissner, Wassilios G. , Ostrowitzki, Susanne, Piantadosi, Steven , Roemer, Cyndi, Schenk, Dale, Schlossmacher, Michael G. , Seppi, Klaus , Shih, Lily, Siderowf, Andrew , Stebbins, Glenn T. , Stefanova, Nadia , Sutton, Sharon Egretta, Zhang, Jing , Halliday, Glenda , Koroshetz, Walter J. , Holton, Janice, Quinn, Niall P, Brooks, David J. , Hewitt, Art, Huentelman, Matt J, Jensen, Poul H, Kellerman, Lawrence, Kim, Woojin Scott, Langer, Carol, LeWitt, Peter, Meissner, Wassilios, Melki, Ronald, Poewe, Werner, Schlossmacher, Michael, Schmahmann, Jeremy D, Tsuji, Shoji , Sutton, Sharon, Kaufmann, Horacio , Meissner, Wassilios G , Höglinger, Günter U , Krismer, Florian , Seppi, Klaus , Cummings, Jeffrey L. , Fortier, P, Freeman, Roy L. , LeWitt, Peter A. , Melki, Ronald , Poewe, Werner H , Robertson, David L. , Schmahmann, Jeremy Dan , Sutton, Sharon

Neurology | December 13, 2017 | Volume: 90 | Issue: 2 | Pages: 74-82

10.1212/wnl.0000000000004798 Get It

Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72‐associated amyotrophic lateral sclerosis
Daughrity, Lillian M. , Diehl, Nancy N. , Wuu, Joanne , Miller, Timothy M. , Pástor, Pau , Trojanowski, John Q. , Hu, William T. , Ratti, Antonia , Benatar, Michael , Glass, Jonathan, Floeter, Mary Kay, Jeromin, Andreas, Petrucelli, Leonard , Group, the C9ORF72 Neurofilament Study, Toledo, Jon B. , Prudencio, Mercedes , Morelli, Claudia , Poletti, Barbara , Gendron, Tania F. , Boylan, Kevin B, Heckman, Michael G. , Grossman, Murray , Berry, James D. , Silani, Vincenzo , Boylan, Khrista , Group, the C9ORF72 Neurofilament Study, Prudencio, Mercedes , Poletti, Barbara , Pastor, Pau , Hu, William T.

Annals of Neurology | June 19, 2017 | Volume: 82 | Issue: 1 | Pages: 139-146

10.1002/ana.24980 Get It

As potential treatments for C9ORF72‐associated amyotrophic lateral sclerosis (c9ALS) approach clinical trials, the identification of prognostic biomarkers for c9ALS becomes a priority. We show that levels of phosphorylated neurofilament heavy chain (pNFH) in cerebrospinal fluid (CSF) predict disease status and survival in c9ALS patients, and are largely stable over time. Moreover, c9ALS patients exhibit higher pNFH levels, more rapid disease progression, and shorter survival after disease onset than ALS patients without C9ORF72 expansions. These data support the use of CSF pNFH as a prognostic biomarker for clinical trials, which will increase the likelihood of successfully developing a treatment for c9ALS. Ann Neurol 2017;82:139–146
Blood‐based biomarkers in Alzheimer disease: Current state of the science and a novel collaborative paradigm for advancing from discovery to clinic
Lista, Simone , Vanderstichele, Hugo, Posner, Holly, Hall, James , Johnson, Leigh , Fong, Y L, Luthman, Johan, Jeromin, Andreas, Batrla‐Utermann, Richard, Villarreal, Alcibiades E. , Britton, Gabrielle B. , Snyder, Peter J. , Henriksen, Kim , Grammas, Paula , Gupta, Veer Bala , Martins, Ralph N. , Hampel, Harald , Area, Biofluid Based Biomarker Professional Interest, O’Bryant, Sid E. , Mielke, Michelle M. , Rissman, Robert A. , Zetterberg, Henrik , Lewczuk, Piotr , Area, Biofluid Based Biomarker Professional Interest

Alzheimer's & Dementia | November 18, 2016 | Volume: 13 | Issue: 1 | Pages: 45-58

10.1016/j.jalz.2016.09.014 Get It

AbstractThe last decade has seen a substantial increase in research focused on the identification of blood‐based biomarkers that have utility in Alzheimer's disease (AD). Blood‐based biomarkers have significant advantages of being time‐ and cost‐efficient as well as reduced invasiveness and increased patient acceptance. Despite these advantages and increased research efforts, the field has been hampered by lack of reproducibility and an unclear path for moving basic discovery toward clinical utilization. Here we reviewed the recent literature on blood‐based biomarkers in AD to provide a current state of the art. In addition, a collaborative model is proposed that leverages academic and industry strengths to facilitate the field in moving past discovery only work and toward clinical use. Key resources are provided. This new public‐private partnership model is intended to circumvent the traditional handoff model and provide a clear and useful paradigm for the advancement of biomarker science in AD and other neurodegenerative diseases.
Comparing biological markers of Alzheimer's disease across blood fraction and platforms: Comparing apples to oranges
O’Bryant, Sid E. , Lista, Simone , Zhang, Fan , Hall, James , Lovestone, Simon , Gupta, Veer Bala , Graff‐Radford, Neill, Martins, Ralph N. , Jeromin, Andreas, Kling, Mitchel A. , Hampel, Harald , Area, ISTAART Blood Based Biomarker Professional Interest, Rissman, Robert A. , Edwards, Melissa , Zetterberg, Henrik , Graff‐Radford, Neill, Waring, Stephen C. , Oh, Esther S , Baker, Laura D. , Area, ISTAART Blood Based Biomarker Professional Interest, O'Bryant, Sid

Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring | December 29, 2015 | Volume: 3 | Issue: 1 | Pages: 27-34

10.1016/j.dadm.2015.12.003 Get It

AbstractIntroductionThis study investigated the comparability of potential Alzheimer's disease (AD) biomarkers across blood fractions and assay platforms.MethodsNonfasting serum and plasma samples from 300 participants (150 AD patients and 150 controls) were analyzed. Proteomic markers were obtained via electrochemiluminescence or Luminex technology. Comparisons were conducted via Pearson correlations. The relative importance of proteins within an AD diagnostic profile was examined using random forest importance plots.ResultsOn the Meso Scale Discovery multiplex platform, 10 of the 21 markers shared >50% of the variance across blood fractions (serum amyloid A R2 = 0.99, interleukin (IL)10 R2 = 0.95, fatty acid‐binding protein (FABP) R2 = 0.94, I309 R2 = 0.94, IL‐5 R2 = 0.94, IL‐6 R2 = 0.94, eotaxin3 R2 = 0.91, IL‐18 R2 = 0.87, soluble tumor necrosis factor receptor 1 R2 = 0.85, and pancreatic polypeptide R2 = 0.81). When examining protein concentrations across platforms, only five markers shared >50% of the variance (beta 2 microglobulin R2 = 0.92, IL‐18 R2 = 0.80, factor VII R2 = 0.78, CRP R2 = 0.74, and FABP R2 = 0.70).DiscussionThe current findings highlight the importance of considering blood fractions and assay platforms when searching for AD relevant biomarkers.
ALS biomarkers for therapy development: State of the field and future directions
Benatar, Michael , Jeromin, Andreas, Rutkove, Seward B. , Atassi, Nazem , Bruijn, Lucie, Boylan, Kevin, Boylan, Khrista , Berry, James D.

Muscle & Nerve | November 17, 2015 | Volume: 53 | Issue: 2 | Pages: 169-182

10.1002/mus.24979 Get It

Guidelines for the standardization of preanalytic variables for blood‐based biomarker studies in Alzheimer's disease research
O’Bryant, Sid E. , Gupta, Veer Bala , Henriksen, Kim , Jeromin, Andreas, Lista, Simone , Bazenet, Chantal, Soares, Holly , Lovestone, Simon , Hampel, Harald , Montine, Thomas J. , Blennow, Kaj , Foroud, Tatiana, Carrillo, María C. , Graff‐Radford, Neill R. , Laske, Christoph , Breteler, Monique M.B. , Shaw, Leslie M. , Trojanowski, John Q. , Schupf, Nicole , Fagan, Anne M. , Oberoi, Pankaj, Umek, Robert M., Weiner, Michael W. , Grammas, Paula , Posner, Holly, Martins, Ralph N. , groups, STAR-B and BBBIG working, Edwards, Melissa , Rissman, Robert A. , groups, STAR-B and BBBIG working, O'Bryant, Sid

Alzheimer's & Dementia | October 1, 2014 | Volume: 11 | Issue: 5 | Pages: 549-560

10.1016/j.jalz.2014.08.099 Get It

Abstract The lack of readily available biomarkers is a significant hindrance toward progressing to effective therapeutic and preventative strategies for Alzheimer's disease (AD). Blood‐based biomarkers have potential to overcome access and cost barriers and greatly facilitate advanced neuroimaging and cerebrospinal fluid biomarker approaches. Despite the fact that preanalytical processing is the largest source of variability in laboratory testing, there are no currently available standardized preanalytical guidelines. The current international working group provides the initial starting point for such guidelines for standardized operating procedures (SOPs). It is anticipated that these guidelines will be updated as additional research findings become available. The statement provides (1) a synopsis of selected preanalytical methods utilized in many international AD cohort studies, (2) initial draft guidelines/SOPs for preanalytical methods, and (3) a list of required methodological information and protocols to be made available for publications in the field to foster cross‐validation across cohorts and laboratories.
Developing novel blood‐based biomarkers for Alzheimer's disease
Snyder, Heather M. , Carrillo, María C. , Henriksen, Kim , Jeromin, Andreas, Lovestone, Simon , Mielke, Michelle M. , O’Bryant, Sid E. , Sarasa, M., Sj⊘gren, Magnus, Soares, Holly , Teeling, Jessica L. , Trushina, Eugenia , Ward, Malcolm , West, Tim , Bain, Lisa J. , Shineman, Diana W., Weiner, Michael W. , Fillit, Howard , Grodstein, Francine , Mielke, Michelle M , Trushina, Eugenia , O'Bryant, Sid

Alzheimer's & Dementia | December 21, 2013 | Volume: 10 | Issue: 1 | Pages: 109-114

10.1016/j.jalz.2013.10.007 Get It

AbstractAlzheimer's disease is the public health crisis of the 21st century. There is a clear need for a widely available, inexpensive and reliable method to diagnosis Alzheimer's disease in the earliest stages, track disease progression, and accelerate clinical development of new therapeutics. One avenue of research being explored is blood based biomarkers. In April 2012, the Alzheimer's Association and the Alzheimer's Drug Discovery Foundation convened top scientists from around the world to discuss the state of blood based biomarker development. This manuscript summarizes the meeting and the resultant discussion, including potential next steps to move this area of research forward.