normal and pathological development of the nervous system

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Editorial Normal and pathological development of the nervous system The 80th annual meeting of the ARNMD was devoted to the study of normal and pathological development. Drs Judith Rapoport and Guy McKhann joined me in organiz- ing the meeting. It proved to be an excellent moment for discussion of this topic. Recent years have seen a decisive move in neuroscience toward an understanding of plasti- city and change. While plasticity is a lifelong phenom- enon, the organization of the nervous system prior to birth and in the years of infancy and childhood provide striking changes in behavior that relate to the development of neural circuits. A theme of the meeting was to view pathology in relation to these normal developmental processes. The meeting began with evidence of changes in neurons and synapses that might illuminate the circuitry involved in developmental disorders. Two of these papers presented by Hastings and by McKay are contained in this volume. The startling discoveries of life long neurogenesis and the abil- ity to form working synapses from cultured stem cells provided a dramatic backdrop to the potentials that might become available for aiding human function and treating disorders. The next session dealt with genetics in relation to normal development and developmental disorders. Papers were presented on learning and memory (Silva), dyslexia (Gala- burda), Williams disease (Bellugi & Klima), Alzheimer’s dementia (Reiman) and attention deficit/hyperactivity disor- der (Swanson) which taken together illustrated a variety of methods for discovering the genetic basis of functions and disorders. The importance of careful definition of phenotypes and the specification of pathways to link muta- tions to affected brain pathways were basic to all the talks. The possibility of using asymptomatic patients in the early treatment of disorders and the need to combine the study of human disorders with the use of animal and cellular approaches were among the many issues raised in these papers. The final session of the first day emphasized the devel- opment of normal functions of perception, attention and language. Studies of children who had cataracts removed at varying ages revealed quite different time periods sensi- tive to the role of experience for various aspects of visual acuity (Maurer). Dr Neville presented a similar theme. Individuals born blind or deaf were studied to examine the influence of sensory deprivation. Experiments suggest that the impact of sensory experience seemed to differ between dorsal and ventral visual and perhaps auditory information processing streams. The first day was concluded with the Salmon lecture. In this lecture I presented studies conducted at the Sackler institute that involved aspects of the development of attention apparent at three periods of infancy and child- hood. In discussing the future of the Institute I sought to tie attentional networks to cellular and genetic mechan- isms on the one hand and, on the other hand, to the acquisition of high level skills learned in school such as literacy. The second day of the meeting was concerned with studies of specific clinical syndromes. Casey outlined the role of striatal-frontal circuits in a number of developmental disorders. She illustrated how these disorders showed distinct patterns of deficit in stimulus and response selec- tion. The development of regional brain areas can be traced non-invasively in longitudinal studies using magnetic reso- nance imaging. Rapoport reported that her team of research- ers at NIMH found a very distinctive pattern of reduced gray matter in child onset schizophrenia that appeared first in posterior sites and only later in anterior regions. Shaywitz presented brain-imaging evidence showing that developmental dyslexia involves a difficulty in auto- matic activation of posterior brain regions that translate visual input into phonolology. Nelson reported on new studies of the concentration of neuropeptides and neurotro- phins in neonatal blood of normal children compared to those later diagnosed with autism, mental retardation, or cerebral palsy. Some quite specific indicants of autism were found that could be used for early diagnosis of the disorder. Overall the meeting was characterized by a feeling of great optimism. This was fostered by ability to communi- cate across many levels of analysis that was illustrated by the meeting and by the papers in this volume. It was clear that new methods and findings were rapidly increasing our understanding of both normal and pathological conditions in Clinical Neuroscience Research 1 (2001) 173–174 1566-2772/01/$ - see front matter q 2001 Association for Research in Nervous and Mental Disease. Published by Elsevier Science B.V. All rights reserved. PII: S1566-2772(01)00002-0 www.elsevier.nl/locate/clires

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Page 1: Normal and pathological development of the nervous system

Editorial

Normal and pathological development of the nervous system

The 80th annual meeting of the ARNMD was devoted

to the study of normal and pathological development. Drs

Judith Rapoport and Guy McKhann joined me in organiz-

ing the meeting. It proved to be an excellent moment for

discussion of this topic. Recent years have seen a decisive

move in neuroscience toward an understanding of plasti-

city and change. While plasticity is a lifelong phenom-

enon, the organization of the nervous system prior to

birth and in the years of infancy and childhood provide

striking changes in behavior that relate to the development

of neural circuits. A theme of the meeting was to view

pathology in relation to these normal developmental

processes.

The meeting began with evidence of changes in neurons

and synapses that might illuminate the circuitry involved in

developmental disorders. Two of these papers presented by

Hastings and by McKay are contained in this volume. The

startling discoveries of life long neurogenesis and the abil-

ity to form working synapses from cultured stem cells

provided a dramatic backdrop to the potentials that might

become available for aiding human function and treating

disorders.

The next session dealt with genetics in relation to normal

development and developmental disorders. Papers were

presented on learning and memory (Silva), dyslexia (Gala-

burda), Williams disease (Bellugi & Klima), Alzheimer's

dementia (Reiman) and attention de®cit/hyperactivity disor-

der (Swanson) which taken together illustrated a variety of

methods for discovering the genetic basis of functions

and disorders. The importance of careful de®nition of

phenotypes and the speci®cation of pathways to link muta-

tions to affected brain pathways were basic to all the talks.

The possibility of using asymptomatic patients in the early

treatment of disorders and the need to combine the study of

human disorders with the use of animal and cellular

approaches were among the many issues raised in these

papers.

The ®nal session of the ®rst day emphasized the devel-

opment of normal functions of perception, attention and

language. Studies of children who had cataracts removed

at varying ages revealed quite different time periods sensi-

tive to the role of experience for various aspects of visual

acuity (Maurer). Dr Neville presented a similar theme.

Individuals born blind or deaf were studied to examine

the in¯uence of sensory deprivation. Experiments suggest

that the impact of sensory experience seemed to differ

between dorsal and ventral visual and perhaps auditory

information processing streams.

The ®rst day was concluded with the Salmon lecture.

In this lecture I presented studies conducted at the Sackler

institute that involved aspects of the development of

attention apparent at three periods of infancy and child-

hood. In discussing the future of the Institute I sought

to tie attentional networks to cellular and genetic mechan-

isms on the one hand and, on the other hand, to the

acquisition of high level skills learned in school such as

literacy.

The second day of the meeting was concerned with

studies of speci®c clinical syndromes. Casey outlined the

role of striatal-frontal circuits in a number of developmental

disorders. She illustrated how these disorders showed

distinct patterns of de®cit in stimulus and response selec-

tion. The development of regional brain areas can be traced

non-invasively in longitudinal studies using magnetic reso-

nance imaging. Rapoport reported that her team of research-

ers at NIMH found a very distinctive pattern of reduced

gray matter in child onset schizophrenia that appeared

®rst in posterior sites and only later in anterior regions.

Shaywitz presented brain-imaging evidence showing

that developmental dyslexia involves a dif®culty in auto-

matic activation of posterior brain regions that translate

visual input into phonolology. Nelson reported on new

studies of the concentration of neuropeptides and neurotro-

phins in neonatal blood of normal children compared to

those later diagnosed with autism, mental retardation, or

cerebral palsy. Some quite speci®c indicants of autism

were found that could be used for early diagnosis of the

disorder.

Overall the meeting was characterized by a feeling of

great optimism. This was fostered by ability to communi-

cate across many levels of analysis that was illustrated by

the meeting and by the papers in this volume. It was clear

that new methods and ®ndings were rapidly increasing our

understanding of both normal and pathological conditions in

Clinical Neuroscience Research 1 (2001) 173±174

1566-2772/01/$ - see front matter q 2001 Association for Research in Nervous and Mental Disease. Published by Elsevier Science B.V. All rights reserved.

PII: S1566-2772(01)00002-0

www.elsevier.nl/locate/clires

Page 2: Normal and pathological development of the nervous system

the development of the human brain and in some cases

providing us with the tools to develop and assess new meth-

ods of treatment. I hope that the readers of these papers will

share a similar feeling of excitement and progress of those

that attended and presented at the meeting.

Michael I. Posner

Sackler Institute, Weill Medical College,

1300 York Avenue, Box 140,

New York NY 10021,

USA

Editorial174

E-mail address: [email protected] (M.I. Posner).