Locus coeruleus neuron density and parkinsonism in older adults without Parkinson's disease

Previous work has showed that nigral neuron density is related to the severity of parkinsonism proximate to death in older persons without a clinical diagnosis of Parkinson's disease (PD). We tested the hypothesis that neuron density in other brain stem aminergic nuclei is also related to the severity of parkinsonism. We studied brain autopsies from 125 deceased older adults without PD enrolled in the Memory and Aging Project, a clinicopathologic investigation. Parkinsonism was assessed with a modified version of the Unified Parkinson's Disease Rating Scale (UPDRS). We measured neuron density in the substantia nigra, ventral tegmental area, locus coeruleus, and dorsal raphe, along with postmortem indices of Lewy body disease, Alzheimer's disease and cerebrovascular pathologies. Mean age at death was 88.0 years, and global parkinsonism was 14.8 (SD, 9.50). In a series of regression models that controlled for demographics and neuron density in the substantia nigra, neuron density in the locus coeruleus (estimate, −0.261; SE, 0.117; P = .028) but not in the ventral tegmental area or dorsal raphe was associated with severity of global parkinsonism proximate to death. These findings were unchanged in models that controlled for postmortem interval, whole‐brain weight, and other common neuropathologies including Alzheimer's disease and Lewy body pathology and cerebrovascular vascular pathologies. In older adults without a clinical diagnosis of PD, neuron density in locus coeruleus nuclei is associated with the severity of parkinsonism and may contribute to late‐life motor impairments. © 2012 Movement Disorder Society

[1]  Chris Zarow,et al.  Neuronal loss is greater in the locus coeruleus than nucleus basalis and substantia nigra in Alzheimer and Parkinson diseases. , 2003, Archives of neurology.

[2]  K. Rommelfanger,et al.  Norepinephrine: The redheaded stepchild of Parkinson's disease. , 2007, Biochemical pharmacology.

[3]  K. Deisseroth,et al.  Tuning arousal with optogenetic modulation of locus coeruleus neurons , 2010, Nature Neuroscience.

[4]  P. Cavallari,et al.  Human Neuroscience Hypothesis and Theory Article a Role for Locus Coeruleus in Parkinson Tremor , 2022 .

[5]  S. Leurgans,et al.  Combinations of motor measures more strongly predict adverse health outcomes in old age: the rush memory and aging project, a community-based cohort study , 2011, BMC Medicine.

[6]  D. Dickson,et al.  Evidence that incidental Lewy body disease is pre-symptomatic Parkinson’s disease , 2008, Acta Neuropathologica.

[7]  E. Louis,et al.  Mild Parkinsonian signs: An overview of an emerging concept , 2007, Movement disorders : official journal of the Movement Disorder Society.

[8]  L. Goodman,et al.  The Pharmacological Basis of Therapeutics , 1941 .

[9]  C. Finley,et al.  Structure of the Human Brain , 1976 .

[10]  H. Braak,et al.  Staging of brain pathology related to sporadic Parkinson’s disease , 2003, Neurobiology of Aging.

[11]  A. Bonnet,et al.  Motor score of the Unified Parkinson Disease Rating Scale as a good predictor of Lewy body-associated neuronal loss in the substantia nigra. , 2006, Archives of neurology.

[12]  D. Bennett,et al.  Dimensionality of parkinsonian signs in aging and Alzheimer's disease. , 1999, The journals of gerontology. Series A, Biological sciences and medical sciences.

[13]  D. Dickson,et al.  Incidental Lewy body disease and preclinical Parkinson disease. , 2008, Archives of neurology.

[14]  Thomas Gasser,et al.  Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria , 2009, The Lancet Neurology.

[15]  K. Jellinger,et al.  Critical evaluation of the Braak staging scheme for Parkinson's disease , 2010, Annals of neurology.

[16]  Clifford B Saper,et al.  Spinal projections of the A5, A6 (locus coeruleus), and A7 noradrenergic cell groups in rats , 2012, The Journal of comparative neurology.

[17]  A. Lees,et al.  Ageing and Parkinson's disease: substantia nigra regional selectivity. , 1991, Brain : a journal of neurology.

[18]  N. Schupf,et al.  Mild parkinsonian signs are associated with increased risk of dementia in a prospective, population‐based study of elders , 2010, Movement disorders : official journal of the Movement Disorder Society.

[19]  B. Yan,et al.  Association between mild parkinsonian signs and mortality in an elderly male cohort in China , 2010, Journal of Clinical Neuroscience.

[20]  S. Leurgans,et al.  Nigral pathology and parkinsonian signs in elders without Parkinson disease , 2012, Annals of neurology.

[21]  J. Schneider,et al.  The effect of social networks on the relation between Alzheimer's disease pathology and level of cognitive function in old people: a longitudinal cohort study , 2006, The Lancet Neurology.

[22]  News Report , 1969 .

[23]  C. Tanner,et al.  Parkinsonian signs and substantia nigra neuron density in decendents elders without PD , 2004, Annals of neurology.

[24]  D. Maraganore,et al.  Comparison of risk factor profiles in incidental Lewy body disease and Parkinson disease. , 2009, Archives of neurology.

[25]  J. Schneider,et al.  Overview and findings from the rush Memory and Aging Project. , 2012, Current Alzheimer research.

[26]  Stephen J. DeArmond,et al.  Structure of the human brain : a photographic atlas , 1974 .