Loss of functional connectivity is an early imaging marker in primary lateral sclerosis

References

• Statland JM, Barohn RJ, Dimachkie MM, Floeter MK, Mitsumoto H. Primary lateral sclerosis. Neurol Clin. 2015;33:749–60.
   PubMed Web of Science ®Google Scholar
• Tartaglia MC, Rowe A, Findlater K, Orange JB, Grace G, Strong MJ, et al. Differentiation between primary lateral sclerosis and amyotrophic lateral sclerosis: examination of symptoms and signs at disease onset and during follow-up. Arch Neurol. 2007;64:232–6.
   PubMedGoogle Scholar
• Gordon PH, Cheng B, Katz IB, Pinto M, Hays AP, Mitsumoto H, et al. The natural history of primary lateral sclerosis. Neurology. 2006;66:647–53.
   PubMed Web of Science ®Google Scholar
• Floeter MK, Mills R. Progression in primary lateral sclerosis: a prospective analysis. Amyotroph Lateral Scler. 2009;10:339–46.
   PubMed Web of Science ®Google Scholar
• Pringle CE, Hudson AJ, Munoz DG, Kiernan JA, Brown WF, Ebers GC, et al. Primary lateral sclerosis. Clinical features, neuropathology and diagnostic criteria. Brain. 1992;115:495–520.
   PubMed Web of Science ®Google Scholar
• Singer MA, Statland JM, Wolfe GI, Barohn RJ. Primary lateral sclerosis. Muscle Nerve. 2007;35:291–302.
   PubMed Web of Science ®Google Scholar
• Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP. Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS. Neurology. 2009;72:1948–52.
   PubMed Web of Science ®Google Scholar
• Kwan JY, Meoded A, Danielian LE, Wu T, Floeter MK. Structural imaging differences and longitudinal changes in primary lateral sclerosis and amyotrophic lateral sclerosis. Neuroimage. 2013;2:151–60.
   Web of Science ®Google Scholar
• Tartaglia MC, Laluz V, Rowe A, Findlater K, Lee DH, Kennedy K, et al. Brain atrophy in primary lateral sclerosis. Neurology. 2009;72:1236–41.
   PubMed Web of Science ®Google Scholar
• Kolind S, Sharma R, Knight S, Johansen-Berg H, Talbot K, et al. Myelin imaging in amyotrophic and primary lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14:562–73.
   PubMed Web of Science ®Google Scholar
• Menke RAL, Abraham I, Thiel CS, Filippini N, Knight S, Talbot K, et al. Fractional anisotropy in the posterior limb of the internal capsule and prognosis in amyotrophic lateral sclerosis. Arch Neurol. 2012;69:1493–9.
   PubMedGoogle Scholar
• Iwata NK, Kwan JY, Danielian LE, Butman JA, Tovar-Moll F, Bayat E, et al. White matter alterations differ in primary lateral sclerosis and amyotrophic lateral sclerosis. Brain. 2011;134:2642–55.
   PubMed Web of Science ®Google Scholar
• Filippini N, Douaud G, Mackay CE, Knight S, Talbot K, Turner MR, et al. Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis. Neurology. 2010;75:1645–52.
   PubMed Web of Science ®Google Scholar
• Meoded A, Morrissette AE, Katipally R, Schanz O, Gotts SJ, Floeter MK, et al. Cerebro-cerebellar connectivity is increased in primary lateral sclerosis. Neuroimage Clin. 2015;7:288–96.
   PubMed Web of Science ®Google Scholar
• Agosta F, Canu E, Inuggi A, Chiò A, Riva N, Silani V, et al. Resting state functional connectivity alterations in primary lateral sclerosis. Neurobiol Aging. 2014;35:916–25.
   PubMed Web of Science ®Google Scholar
• Folstein MF, Folstein SE, McHugh PR. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975;12:189–98.
   PubMed Web of Science ®Google Scholar
• Sarlls JE, Pierpaoli C, Talagala SL, Luh WM. Robust fat suppression at 3T in high-resolution diffusion-weighted single-shot echo-planar imaging of human brain. Magn Reson Med. 2011;66:1658–65.
   PubMed Web of Science ®Google Scholar
• Worsley KJ. Statistical analysis of activation images. In: Jezzard P, Matthews PM, Smith SM, eds. Functional MRI: an introduction to methods. Oxford GB: Oxford Medical Publications; 2001:251–270.
   Google Scholar
• Desikan RS, Ségonne F, Fischl B, Quinn BT, Dickerson BC, Blacker D, et al. An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest. Neuroimage 2006;31:968–80.
   PubMed Web of Science ®Google Scholar
• Reuter M, Schmansky NJ, Rosas HD, Fischl B. Within-subject template estimation for unbiased longitudinal image analysis. Neuroimage. 2012;61:1402–18.
   PubMed Web of Science ®Google Scholar
• Smith SM, Jenkinson M, Johansen-Berg H, Rueckert D, Nichols TE, Mackay CE, et al. Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data. Neuroimage. 2006;31:1487–505.
   PubMed Web of Science ®Google Scholar
• Danielian LE, Iwata NK, Thomasson DM, Floeter MK. Reliability of fiber tracking measurements in diffusion tensor imaging for longitudinal study. Neuroimage. 2010;49:1572–80.
   PubMed Web of Science ®Google Scholar
• Hofer S, Frahm J. Topography of the human corpus callosum revisited – comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage. 2006;32:989–94.
   PubMed Web of Science ®Google Scholar
• Floeter MK, Bageac D, Danielian LE, Braun LE, Traynor BJ, Kwan JY, et al. Longitudinal imaging in C9orf72 mutation carriers: relationship to phenotype. Neuroimage Clin. 2016;12:1035–43.
   PubMed Web of Science ®Google Scholar
• Proudfoot M, Colclough GL, Quinn A, Wuu J, Talbot K, Benatar M, et al. Increased cerebral functional connectivity in ALS: a resting-state magnetoencephalography study. Neurology. 2018;90:e1418–24.
   PubMed Web of Science ®Google Scholar
• Joel SE, Caffo BS, van Zijl PC, Pekar JJ. On the relationship between seed-based and ICA-based measures of functional connectivity. Magn Reson Med. 2011;66:644–57.
   PubMed Web of Science ®Google Scholar
• van den Heuvel MP, Mandl RC, Kahn RS, Hulshoff Pol HE. Functionally linked resting-state networks reflect the underlying structural connectivity architecture of the human brain. Hum Brain Mapp. 2009;30:3127–41.
   PubMed Web of Science ®Google Scholar
• Fling BW, Benson BL, Seidler RD. Transcallosal sensorimotor fiber tract structure–function relationships. Hum Brain Mapp. 2013;34:384–95.
   PubMed Web of Science ®Google Scholar
• Tazoe T, Perez MA. Speed-dependent contribution of callosal pathways to ipsilateral movements. J Neurosci. 2013;33:16178–88.
   PubMed Web of Science ®Google Scholar
• Douaud G, Filippini N, Knight S, Talbot K, Turner MR. Integration of structural and functional magnetic resonance imaging in amyotrophic lateral sclerosis. Brain. 2011;134:3470–9.
   PubMed Web of Science ®Google Scholar
• Maekawa S, Al‐Sarraj S, Kibble M, Landau S, Parnavelas J, Cotter D, et al. Cortical selective vulnerability in motor neuron disease: a morphometric study. Brain. 2004;127:1237–51.
   PubMed Web of Science ®Google Scholar
• Sehm B, Steele CJ, Villringer A, Ragert P. Mirror motor activity during right-hand contractions and its relation to white matter in the posterior midbody of the corpus callosum. Cereb Cortex. 2016;26:4347–55.
   PubMed Web of Science ®Google Scholar
• Betzel RF, Byrge L, He Y, Goñi J, Zuo X-N, Sporns O, et al. Changes in structural and functional connectivity among resting-state networks across the human lifespan. Neuroimage. 2014;102: 345–57.
   PubMed Web of Science ®Google Scholar
• Fling BW, Seidler RD. Fundamental differences in callosal structure, neurophysiologic function, and bimanual control in young and older adults. Cereb Cortex. 2012;22:2643–52.
   PubMed Web of Science ®Google Scholar
• He H, Luo C, Chang X, Shan Y, Cao W, Gong J, et al. The functional integration in the sensory-motor system predicts aging in healthy older adults. Front Aging Neurosci. 2017;8:306.
   PubMed Web of Science ®Google Scholar