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Sánchez-Contreras, Mónica

https://orcid.org/0000-0002-3092-2781

Mayo Clinic

University of Washington

Citations 16

The longevity effects of reduced IGF-1 signaling depend on the stability of the mitochondrial genome
Shemtov, Sarah J. , McGann, Eric, Carrillo, Lucy , Lee, Sangmin , Anson, Herbert, Chung, Claire S, Weinert, Jaye L., Anagnostou, Maria-Eleni, Lai, Guan-Ju, Verheijen, Bert M. , Wan, Junxiang , Vorobyova, Ivetta, Sanchez-Contreras, Monica, Conover, Cheryl A. , Thorwald, Max A. , Cohen, P., Kennedy, Scott R. , Goût, Jean-François , Haroon, Suraiya , Vermulst, Marc , Hwang, Eric , Chung, Claire S , Weinert, Jaye L , Lai, Guan-Ju D , Conover, Cheryl A , Thorwald, Max A , Cohen, Pinchas , Kennedy, Scott R , Gout, Jean-François , Vermulst, Marc , Anagnostou, Maria‐Eleni, Sánchez-Contreras, Mónica , Cohen, Pinchas

Science Advances | April 3, 2026 | Volume: 12 | Issue: 14 | Pages: No page available

10.1126/sciadv.aea4279 Get It

Suppression of insulin-like growth factor-1 (IGF-1) signaling extends mammalian life span and protects against a range of age-related diseases. Unexpectedly, we found that reduced IGF-1 signaling fails to extend the life span of mitochondrial mutator mice. Most of the longevity pathways that are normally initiated by IGF-1 suppression were either blocked or blunted in the mutator mice. These observations suggest that the prolongevity effects of IGF-1 suppression critically depend on the integrity of the mitochondrial genome, revealing an unexpected hierarchy in the pathways that control mammalian aging. Together, these findings deepen our understanding of the interactions between the hallmarks of aging and underscore the need for interventions that preserve the integrity of the mitochondrial genome.
Three Sib-Pairs of Autopsy-Confirmed Progressive Supranuclear Palsy (P5.248)
Strongosky, Audrey , Ogaki, Kotaro, Whaley, Nathaniel R., Tacik, Paweł , Gerpen, Jay Van, Uitti, Ryan J. , Rademakers, Rosa , Fujioka, Shinsuke , Sánchez-Contreras, Mónica , Gerpen, Jay A. van, Ross, Owen A. , Wszołek, Zbigniew K. , Dickson, Dennis W.

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.p5.248 Get It

A Family With Corticobasal Degeneration, Parkinson’s Disease, Amyotrophic Lateral Sclerosis, and Dementia (P3.085)
Strongosky, Audrey , Tacik, Paweł , Rademakers, Rosa , Fujioka, Shinsuke , Sánchez-Contreras, Mónica , Boeve, Bradley F. , Stoessl, A. Jon , Baker, Matthew, Dickson, Dennis W. , Wszołek, Zbigniew K.

Neurology | December 7, 2023 | Volume: 82 | Issue: 10_supplement | Pages: No page available

10.1212/wnl.82.10_supplement.p3.085 Get It

Literature Review of Genetic Disorders with tau Pathology (P5.170)
Tacik, Paweł , Rademakers, Rosa , Wszołek, Zbigniew K. , Sánchez-Contreras, Mónica , Dickson, Dennis W.

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.p5.170 Get It

Literature Review of Genetic Disorders with tau Pathology (I12.004)
Tacik, Paweł , Rademakers, Rosa , Wszołek, Zbigniew K. , Sánchez-Contreras, Mónica , Dickson, Dennis W.

Neurology | December 7, 2023 | Volume: 86 | Issue: 16_supplement | Pages: No page available

10.1212/wnl.86.16_supplement.i12.004 Get It

The novel p.K317N mutation in MAPT gene with clinicopathological phenotype of globular glial tauopathy (P2.161)
Tacik, Paweł , DeTure, Michael , Lin, Wen-Lang, Wojtas, Aleksandra, Walton, Ronald L., Carlomango, Yari, Brown, Patricia E. , Strongosky, Audrey , Josephs, Keith A. , Rademakers, Rosa , Wszołek, Zbigniew K. , Sánchez-Contreras, Mónica , Fujioka, Shinsuke , Baker, Matthew , Brown, Patricia, Kouri, Naomi , Murray, Melissa E. , Ross, Owen A. , Dickson, Dennis W.

Neurology | December 6, 2023 | Volume: 84 | Issue: 14_supplement | Pages: No page available

10.1212/wnl.84.14_supplement.p2.161 Get It

Relationships between lewy and tau pathologies in 375 consecutive non‐Alzheimer's olfactory bulbs
Kasanuki, Koji , Ross, Owen A. , DeTure, Michael , Walton, Ronald L., Koga, Shunsuke , Murray, Melissa E. , Rademakers, Rosa , DeTure, Michael A, Koga, Shunsuke , Ross, Owen A , Murray, Melissa E , Sánchez-Contreras, Mónica , Dickson, Dennis W.

Movement Disorders | January 11, 2018 | Volume: 33 | Issue: 2 | Pages: 333-334

10.1002/mds.27250 Get It

Cognitive impairment in progressive supranuclear palsy is associated with tau burden
Koga, Shunsuke , Parks, Adam , Kasanuki, Koji , Josephs, Keith A. , Ahlskog, J. Eric , Uitti, Ryan J. , Graff‐Radford, Neill R. , Gerpen, Jay A. van, Rademakers, Rosa , Baker, Matthew C, Van Gerpen, Jay A, Koga, Shunsuke , Sánchez-Contreras, Mónica , Baker, Matthew , Wszołek, Zbigniew K. , Dickson, Dennis W.

Movement Disorders | October 30, 2017 | Volume: 32 | Issue: 12 | Pages: 1772-1779

10.1002/mds.27198 Get It

Abstract Background Cognitive impairment is one of the core features of progressive supranuclear palsy. This study aimed to clarify the profile of cognitive impairment and its underlying pathology in progressive supranuclear palsy. Methods We retrospectively reviewed medical records to evaluate the pattern and severity of cognitive impairment in 121 autopsy‐confirmed progressive supranuclear palsy patients. A subset of 37 patients underwent neuropsychological evaluation as part of their clinical workup. The burden of progressive supranuclear palsy‐related tau pathology (neurofibrillary tangles/pretangles, coiled bodies, tufted astrocytes, and threads) was semiquantitatively scored in 20 vulnerable brain regions. Concurrent pathologies potentially associated with cognitive impairment, such as Alzheimer's‐type pathology, were also assessed. To evaluate possible genetic risk factors for cognitive impairment, genetic analysis for APOE and MAPT was performed. Results Ninety patients (74%) had documented cognitive impairment based on neurologic evaluation. In a subgroup with neuropsychological testing (n = 37), executive functioning was the most severely impaired cognitive domain. A global cognitive impairment index (Spearman's rho, −0.49; P = 0.005) and executive functioning were negatively correlated with total tau burden (Spearman's rho, −0.51; P = 0.003), but not correlated with the Alzheimer's‐type pathology. APOE ɛ4 carriers had more severe amyloid pathology, but total tau burden and a global cognitive impairment index did not differ from APOE ɛ4 noncarriers. Conclusion Cognitive impairment in progressive supranuclear palsy, most notably executive dysfunction, is associated with severity of progressive supranuclear palsy‐related tau pathology. © 2017 International Parkinson and Movement Disorder Society