2 December 2011. Dying neurons typically
display little activity, but Alzheimer’s disease researchers have puzzled over
a strange surge of hippocampal firing in some seniors at the cusp of mental
decline. A functional brain imaging study in the November 30 Journal of
Neuroscience links this paradoxical hyperactivity with an established marker of
neuro-degeneration—atrophy
in a network of functionally connected AD brain areas. The correlation showed
up not only in older people with mild cognitive impairment, but also in those
who seemed cognitively normal. The research, led by Reisa Sperling at Brigham
and Women’s Hospital in Boston, suggests that hippocampal hyperactivation in seniors with normal or
slightly impaired cognition could be an early sign of AD-related neurodegeneration.
Functional and structural imaging
evidence continues to push back the start of Alzheimer’s disease by years, even
decades, before memory problems emerge. Just before the steady
decline in hippocampal activation that occurs as dementia sets in, this brain
region shows a surprising frenzy of activity. With functional
magnetic resonance imaging (fMRI), Sperling and others have seen hippocampal hyperactivation in seniors
with MCI (Dickerson et al., 2005; Hämäläinen et al., 2007; Kircher et al., 2007;Yassa et al., 2010) or mildly impaired memory (ARF
related news story onMiller et al., 2008), people with familial or genetic AD risk (Bondi et al., 2005; Bassett et al., 2006), and even in young adults (ARF
related news story on Filippini et al., 2009). Research presented at the recent
Society for Neuroscience meeting in Washington, DC, also suggests that brain
changes revealed by functional imaging could signal future dementia (seeARF
related news story).
Meanwhile, structural MRI studies have
identified a network of functionally connected cortical regions that thin out
in MCI patients on the wane toward AD dementia (Bakkour et al., 2009; Dickerson et al., 2009), and in some cognitively normal
adults (Dickerson et al., 2011). In the current study, first
author Deepti Putcha and colleagues wondered if hippocampal hyperactivity correlated
with cortical thinning in these AD signature areas.
The
researchers used functional and structural MRI to analyze 18 cognitively intact
seniors and 16 with “early MCI.” The latter came from a cohort, recruited for
the second phase of the Alzheimer’s Disease Neuroimaging Initiative (ADNI),
deemed not quite normal but not impaired enough to meet amnestic MCI criteria,
Sperling told ARF. Compared to the control group, early MCI participants did
worse on the Rey auditory verbal learning task and showed modest deficiencies
in Clinical Dementia Rating (CDR) and Mini-Mental State Exam scores. And,
consistent with previous work, the early MCI group showed hippocampal
hyperactivity relative to controls during the fMRI memory task. The new piece
in the present study was the connection to atrophy in AD signature areas shown
by structural MRI. “The more the hippocampus showed this paradoxical
hyperactivity, the greater the cortical thinning in these functionally
connected regions,” Sperling said of the early MCI group. The signature areas
included the medial temporal lobe, the angular gyrus, and the inferior temporal
gyrus. The association also appeared in the control group, albeit only in a
subset of these cortical regions.
“I think this hyperactivity is a
harbinger of imminent clinical decline. This study links it to
neurodegeneration, not just in the hippocampus but in a distributed network of
AD signature regions,” Sperling said. Her findings seem to jibe with recent reports of
increased neuronal excitotoxicity (ARF
related news story on Palop et al., 2007) and abnormally high
calcium influx (ARF related news story) in the hippocampus and
associated cortical regions in AD mouse models.
Though she concedes that fMRI is an
indirect measure of neuronal activity—“much removed” from the direct recordings
done in animal studies—Sperling thinks excitotoxicity could be driving
the paradoxical hyperactivity she and
others have observed in mildly impaired seniors, and even some who appear
normal. “One of the early things that may happen in AD before
cells die is that they have this aberrant increase in activity. When they’re
firing in an abnormal way, that may be a sign that they are dying,” she said. Longitudinal studies are
underway to see if this hypothesis bears out.—Esther Landhuis.
Reference:
Putcha D, Brickhouse M, O’Keefe K, Sullivan C, Rentz D, Marshall G, Dickerson B, Sperling R. Hippocampal Hyperactivation Associated with Cortical Thinning in Alzheimer’s in Non-demented Elderly Adults. J Neurosci. 2011 Nov 30;31(48):17680-17688. Abstract
Putcha D, Brickhouse M, O’Keefe K, Sullivan C, Rentz D, Marshall G, Dickerson B, Sperling R. Hippocampal Hyperactivation Associated with Cortical Thinning in Alzheimer’s in Non-demented Elderly Adults. J Neurosci. 2011 Nov 30;31(48):17680-17688. Abstract

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