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One drawback in understanding
Rett syndrome (RTT), a neurodevelopmental disorder often mistaken for
autism, is the inability to catalog its biology during its course. A study
by SakkuBai Naidu, M.D., and colleagues shows, however, that sampling
patients' nasal epithelium in a simple biopsy provides a window on the illness.
Biopsies contain olfactory receptor neurons. In comparing tissue from RTT
patients with controls, the researchers noted far fewer mature neurons.Those
remaining were physically abnormal. The high numbers of immature neurons
suggest a rise in neurogenesis with failure to mature.
Ann Neurol 2003;54(2):206-218.
Injuries to peripheral nerves are notorious for causing enduring pain.
Common belief holds that nerve regeneration offers relief. James Campbell,
M.D., and his team sought to verify that idea, using a control and two
animal models of neuropathic injury-one with a ligature lesion and the other
with a crush lesion, both at the L5 spinal nerve root in the rat. Nerves
in the latter are more prone to regenerate. Rats were tested periodically
for heightened sensitivity to mechanical and cooling stimuli. Later, tissues
were examined histologically. Both models were hypersensitive to test stimuli.
But, with time, differences between the two appeared in structure and in
response, suggesting nerve regeneration may alleviate pain. This is a key
step in understanding neuropathic pain. It implies that assisting nerve
recovery may control it.
Neurosurgery 2003;53(5):1200-1204.
Literature suggests the MRI technique called fluid attenuation inversion
recovery (FLAIR) may be superior to standard CT in detecting subarachnoid
hemorrhage (SAH). That would be a boon because lumbar puncture holds a high
risk for some patients. But a team of neuroradiologists including Mona
Mohamed, M.D., and David Yousem, M.D., questioned FLAIR's superiority,
comparing it to the gold standard for SAH-revealing-the lumbar puncture.
An unbiased review of 12 patients with negative CT scans but positive lumbar
puncture showed FLAIR within two days of the event didn't fare well: It
concurred with the puncture in only two of the cases. The authors offer
reasons why that might be the case.
Am J Neuroradiol in press.
Difficulty in pinning down the nature of bipolar patients' cycling between
mania and depression is one of psychiatry's dilemmas. In "rapid cycling"
patients, for example, is it that episodes are more frequent or is it the
actual switching that's speeded up? Dean MacKinnon, M.D., Peter Zandi,
Ph.D., J. Raymond DePaulo, M.D., and colleagues favor a closer look
at the switching process, saying the phenomenon may clarify the biology
of bipolar disorder. They've analyzed 608 people in a bipolar genetics study,
including those who report rapid switching and those without it, to find
possible influencing factors-things like onset age and antidepressant. Results
showed those with earlier onset, those with substance abuse or anxiety disorder
or those who've attempted suicide are more prone to rapid switching.
Arch Gen Psychiatry 2003; 60(9):921-934.
Disabling neuropathy is a major side effect of many chemotherapeutic
drugs. Fortunately, for most chemotherapies, the highest dose that avoids
neuropathy has been figured out. But a research team including neurologists
Vinay Chaudhry, M.D., and John Griffin, M.D., suggests that
such "safe" doses may not be safe in patients with pre-existing neuropathy.
They report on six patients who received chemotherapy for cancers or lupus
and who already had neuropathy from causes ranging from diabetes to alcohol
use. All suffered significant worsening of their neuropathy at a "safe"
dose of chemotherapy. Because such neuropathy can be irreversible and resulting
pain can dramatically lower quality of life, careful monitoring of neuropathy-bearing
patients undergoing "chemo" should be the rule. Neurology
2003;60:337-340.
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