2008
DOI: 10.1016/j.jocn.2008.01.010
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Brain flexibility and balance and gait performances mark morphological and metabolic abnormalities in the elderly

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Cited by 9 publications
(7 citation statements)
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“…In general, however, MRS studies have not identified sex differences in NAA levels (cortical gray matter [10,23,36,59,101,109,112], subcortical gray matter [23], supraventricular white matter [23,36,101,103], thalamus [59,101,112], hippocampus [36,59], cerebellum [101], or basal ganglia [8,36,59,112,134] but see [42]).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In general, however, MRS studies have not identified sex differences in NAA levels (cortical gray matter [10,23,36,59,101,109,112], subcortical gray matter [23], supraventricular white matter [23,36,101,103], thalamus [59,101,112], hippocampus [36,59], cerebellum [101], or basal ganglia [8,36,59,112,134] but see [42]).…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies reported either significant [2,45,67,103] or negligible [1,9,24,42,43,64,100,115,119,122] age-related differences in NAA in healthy men and women. In some brain regions, there is evidence both for and against the vulnerability of NAA to age (e.g., frontal: for [16,38], against [20,22,46,56,109]; occipital: for [27], against [109,115]; and basal ganglia: for [22,46], against [6,8,134]), while in other brain regions, evidence is generally consistently for (temporal regions [2], hippocampus [38,118], and midbrain [84]) or consistently against (parietal white matter [46,65,78,115] and pons [30,84]) age-related compromise in NAA levels. Lower levels of striatal NAA with older age might reflect the vulnerability of the striatum to volume loss as suggested by results of in vivo structural imaging [13,44] and postmortem evaluation [107].…”
Section: Discussionmentioning
confidence: 99%
“…Various pathophysiological mechanisms may underlie the found associations of OH with impaired physical functioning, though the present study does not demonstrate these. White matter brain lesions are associated with OH (Aoki et al, 2013;Ben Salem et al, 2008;Starr et al, 2003) and may lead to impaired balance (Aoki et al, 2013;Demain et al, 2014). They are also associated with cognitive impairment (David et al, 2016;Malek et al, 2016), which might be an intermediate factor between OH and impaired ADL performance, as cognitive impairment is associated with both OH and impaired ADL performance (Bocti et al, 2017;Centi et al, 2017;De Vriendt et al, 2015;Dodge et al, 2005;Huang et al, 2017;Mehrabian et al, 2010;Sands et al, 2002).…”
Section: Potential Pathophysiological Mechanisms Involvedmentioning
confidence: 99%
“…OH may negatively affect physical functioning (e.g. balance, gait characteristics, walking speed, exercise tolerance and activities of daily living (ADL)) in older adults through different mechanisms: 1) acute decreased brain perfusion and oxygenation within minutes after postural change (Mager, 2012); 2) chronic brain pathology, such as brain atrophy, microbleeds and white matter brain lesions (Aoki et al, 2013;Ben Salem et al, 2008;Starr et al, 2003); 3) impaired muscle microcirculation, causing poor muscle endurance and pain in neck, buttock and calf muscles (Bleasdale- Barr and Mathias, 1998;Degens et al, 2006;Humm et al, 2011;Robbins et al, 2011). Therefore, OH may cause deterioration of physical functioning.…”
Section: Introductionmentioning
confidence: 99%
“…The signs and symptoms of body balance change can crop up when there is a conflict in the integration of vestibular information, appearing upon rotational dizziness (vertigo) and/or the non-rotational 2 . The physical decline associated with this movement seems to be associated with aging and to non-transmissible chronic diseases 3 , 4 , 5 . In this case, changes associated with aging of the psychomotor, sensorimotor and neuromuscular systems cause the appearance of postural balance problems, thus increasing the risk of falls.…”
Section: Introductionmentioning
confidence: 99%