Read Secondary Schizophrenia Online

Authors: Perminder S. Sachdev

Secondary Schizophrenia (113 page)

BOOK: Secondary Schizophrenia
9.15Mb size Format: txt, pdf, ePub
ads

E. F., Mohan K. Difference

85–90.

American Psychiatric Press, Inc.,

between herpes simplex virus type

7. O’Callaghan E., Sham P. C., Takei

pp. 89–112.

1 and type 2 neonatal encephalitis

N.,
et al.
The relationship of

16. Remington J. S., McLeod R.,

in neurological outcome. Lancet,

schizophrenic births to 16

Thulliez P., Desmonts G. (2001).

1988.
1
(8575–6):1–4.

infectious diseases. Br J

Toxoplasmosis. In Infectious

24. Ingall D., Sanchez P. J. (1995).

Psychiatry, 1994.
165
(3):353–6.

Diseases of the Fetus and Newborn

Syphilis. In Infectious Diseases of

8. Torrey E. F., Rawlings R.,

Infant, Remington J. S. and Klein

the Fetus and Newborn,

Waldman I. N. Schizophrenic

J. O. (Eds.). Philadelphia: W.B.

Remington J. S. and Klein J. O.

births and viral diseases in two

Saunders Company, pp. 205–

(Eds.). Philadelphia: WB

states. Schizophr Res, 1988.

346.

Saunders. p. 652.

1
(1):73–7.

17. Dukes C. S., Luft B. J., Durak D. T.

25. Babulas V., Factor-Litvak P., Goetz

9. Suvisaari J., Haukka J., Tanskanen

(1997). Toxoplasmosis. In

R., Schaefer C. A., Brown A. S.

A., Hovi T., Lönnqvist J.,

Infections of the Central Nervous

Prenatal exposure to maternal

Association between prenatal

System, Scheld W. M., Whitley

genital and reproductive

exposure to poliovirus infection

R. J., and Durack D. T. (Eds).

infections and adult

and adult schizophrenia. Am J

Philadelphia: Lippincott-Raven,

schizophrenia. Am J Psychiatry,

Psychiatry, 1999.
156
(7):1100–2.

pp. 785–806.

2006.
163
(5):927–9.

10. Van Den Berg B. J. The California

18. Brown A. S., Schaefer C. A.,

26. Brown A. S., Cohen P., Greenwald

child health and development

Quesenberry C. P. Jr.,
et al.

S., Susser E. Nonaffective

studies: twenty years of research.

Maternal exposure to

psychosis after prenatal exposure

World Health Stat Q, 1979.

toxoplasmosis and risk of

to rubella. Am J Psychiatry, 2000.

32
(4):269–86.

schizophrenia in adult offspring.

157
(3):438–43.

285

Organic Syndromes of Schizophrenia – Section 3

27. Brown A. S., Cohen P.,

Publ Assoc Res Nerv Ment Dis,

46. Zalewska A., Glowacka E.,

Harkavy-Friedman J.,
et al.
A.E.

1973.
51
:23–62.

Wyczolkowska J.,
et al.
Interleukin

Bennett Research Award. Prenatal

37. Townsend J. J. (1994). Rubella

6 and 8 levels in plasma and

rubella, premorbid abnormalities,

virus disease. In Handbook of

fibroblast cultures in psoriasis.

and adult schizophrenia. Biol

Neurovirology, McKendall R. R.

Mediators Inflamm, 2006.
2006
:
Psychiatry, 2001.
49
(6):
and Stropp W. G. (Eds.). New

81767.

473–86.

York: Marcel Dekker, pp. 603–11.

47. Brown A. S., Susser E. (1999).

28. Chess S., Korn S., Fernandez P.

38. Weizman R., Bessler H. (1999).

Plausibility of prenatal rubella,

(1971). Psychiatric Disorders of

Cytokines: Stress and Immunity.

influenza, and other viral

Children with Congenital Rubella.

In Cytokines: Stress and Immunity,

infections as risk factors for

New York: Brunner/Mazel.

Plotnikoff N. P., Faith R. E., and

schizophrenia. In Prenatal

29. Chess S. Follow-up report on

Murgo A. J.,
et al.
(Eds.). Boca

Exposures in Schizophrenia, Susser

autism in congenital rubella.

Raton, FL: CRC Press,

E., Brown A. S., and Gorman

J Autism Child Schizophr, 1977.

pp. 1–15.

J. M. (Eds.). Washington, DC:

7
(1):69–81.

American Psychiatric Press, Inc.,

39. Shimoya K., Matsuzaki, N.,

pp. 113–31.

30. Eaton W. W. Epidemiology of

Taniguchi T.,
et al.
Interleukin-8

schizophrenia. Epidemiol Rev,

level in maternal serum as a

48. Koenig J. I., Kirkpatrick B., Lee P.

1985.
7
:105–26.

marker for screening of

Glucocorticoid hormones and

early brain development in

31. Kendler K. S., MacLean C. J.,

histological chorioamnionitis at

schizophrenia. Neuropsycho-

O’Neill F. A.,
et al.
Evidence for a
term. Int J Gynaecol Obstet, 1997.

pharmacology, 2002.
27
(2):
schizophrenia vulnerability locus

57
(2):153–9.

309–18.

on chromosome 8p in the Irish

40. Gilmore J. H., Jarskog L. F.

Study of High-Density

Exposure to infection and brain

49. Torrey E. F., Bartko J. J., Lun Z. R.,

Schizophrenia Families. Am J

development: Cytokines in the

Yolken R. H. Antibodies to

Psychiatry, 1996.
153
(12):
pathogenesis of schizophrenia.

toxoplasma gondii in patients

1534–40.

Schizophr Res, 1997.
24
(3):365–7.

with schizophrenia: a

32. Reichenberg A., Weiser M., Rapp

41. Brown A. S., Hooton J., Schaefer

meta-analysis. Schizophr Bull,

M. A.,
et al.
Elaboration on

C. A.,
et al.
Elevated maternal

2007.
33
(3):729–36.

premorbid intellectual

interleukin-8 levels and risk of

50. Anton E. S., Marchionni M. A.,

performance in schizophrenia:

schizophrenia in adult offspring.

Lee K. F.,
et al.
Role of

premorbid intellectual decline

Am J Psychiatry, 2004.
161
(5):
GGF/neuregulin signaling in

and risk for schizophrenia. Arch

889–95.

interactions between migrating

Gen Psychiatry, 2005.
62
(12):
42. Atta-ur-Rahman, Harvey K.,

neurons and radial glia in the

1297–304.

Siddiqui R. A. Interleukin-8: an

developing cerebral cortex.

33. Whitley R. J., Stagno S. (1997).

autocrine inflammatory mediator.

Development, 1997.
124
(18):
Perinatal infections. In Infections

Curr Pharm Des, 1999.
5
(4):
3501–10.

of the Central Nervous System,

241–53.

51. Kamiya A., Kubo K., Tomoda T.,

Scheld W. M., Whitley R. J., and

43. Mukaida N. The roles of cytokine

et al.
A schizophrenia-associated

Durack D. T. (Eds.). Philadelphia:

receptors in diseases. Rinsho

mutation of DISC1 perturbs

Lippincott-Raven Press,

Byori, 2000.
48
(5):409–15.

cerebral cortex development. Nat

pp. 223–53.

Cell Biol, 2005.
7
(12):1167–78.

44. Detmers P. A., La S. K.,

34. Boue J. G., Boue A. Effects of

Olsen-Egbert E.,
et al.

52. Shi L., Fatemi S. H., Sidwell R. W.,

rubella virus infection on the

Neutrophil-activating protein

Patterson P. H. Maternal influenza

division of human cells. Am J Dis

1/interleukin 8 stimulates the

infection causes marked

Child, 1969.
118
(1):45–8.

binding activity of the leukocyte

behavioral and pharmacological

35. Rorke L. B. Nervous system

adhesion receptor CD11b/CD18

changes in the offspring.

lesions in the congenital rubella

on human neutrophils. J Exp Med,

J Neurosci, 2003.
23
(1):297–302.

syndrome. Arch Otolaryngol,

1990.
171
(4):1155–62.

53. Fatemi S. H., Emamian E. S., Kist

1973.
98
(4):249–51.

45. Huber A. R., Kunkel S. L., Todd

D.,
et al.
Defective corticogenesis

36. Kemper T. L., Lecours A. R., Gates

R. F., 3rd, Weiss S. J. Regulation of

and reduction in reelin

M. J., Yakoviev P. I. Retardation of

transendothelial neutrophil

immunoreactivity in cortex and

the myelo-and cytoarchitectonic

migration by endogenous

hippocampus of prenatally

maturation of the brain in the

interleukin-8. Science, 1991.

infected neonatal mice. Mol

286

congenital rubella syndrome. Res

254
(5028):99–102.

Psychiatry, 1999.
4
(2):145–54.

Chapter 22 – Infection and schizophrenia

54. Zuckerman L., Rehavi M.,

mental model of schizophrenia.

Mortal Wkly Rep,
49
(RR-2):
Nachman R., Weiner I. Immune

Neuropsychopharmacology,

57–75. 2000.

activation during pregnancy in

2003.
28
(10):1778–

56. Brown A. S., Schaefer C. A., Wyatt

rats leads to a postpubertal

89.

R. J.,
et al.
Maternal exposure to

emergence of disrupted latent

55. Centers for Disease Control and

respiratory infections and adult

inhibition, dopaminergic

Prevention. CDC

schizophrenia spectrum

hyperfunction, and altered

recommendations regarding

disorders: a prospective birth

limbic morphology in the

selected conditions affecting

cohort study. Schizophr Bull,

offspring: a novel neurodevelop-

women’s health. MMWR Morb

2000.
26
(2):287–95.

287

Section 3

Organic syndromes of schizophrenia: genetic disorders related to SLP

Chapter
23Thestatusofgeneticinvestigations

of schizophrenia

Bryan Mowry

Facts box

SZ
[2],
and in 1946, Kallmann analyzed 691 SZ twin
r

families
[3].
Decades of family
[4],
twin
[5, 6],
and
Schizophrenia (SZ) has a substantial genetic
adoption studies
[7, 8]
have substantiated these early
predisposition.

views indicating a substantial genetic component to
r
The inheritance pattern is complex, likely
SZ risk, with an 80% heritability (the proportion of
involving multiple, commonly occurring risk
the total phenotypic variance explained by genetic fac-variants, each exerting a modest effect on
tors)
[9, 10],
a 50% concordance rate in monozygotic
overall disease risk.

twins, and a 10% risk to siblings relative to a 1% gen-r
Significant progress has recently occurred
eral population risk
[11]
. The inheritance pattern is
with consensus chromosomal regions being

complex (i.e. non-Mendelian), and there are no known
linked to SZ and specific candidate genes,

familial subtypes
[12].
Available data suggest multiple,
often located within these linkage regions,
common SZ variants, each exerting small to moderate
being associated with SZ in multiple

effect on overall disease risk
[12],
possibly interacting
populations with variable ancestry.

with environmental factors
[13]
and epigenetic pro-r
However, indisputable evidence of
cesses
[14]
in a neurodevelopmental context to confer
association is lacking and no allele/haplotype
vulnerability
[15].
An alternative view is that multiple
has yet been conclusively implicated for any
genes are certainly implicated, but that each is highly
candidate gene.

BOOK: Secondary Schizophrenia
9.15Mb size Format: txt, pdf, ePub
ads

Other books

Lost in London by Callaghan, Cindy
The Borrowers Afield by Mary Norton
Garvey's Choice by Nikki Grimes
The Matchmaker by Kay Hooper
The Pledge by Derting, Kimberly
Whiter Than Snow by Sandra Dallas
Transcendent by Katelyn Detweiler
Beneath the Honeysuckle Vine by McClure, Marcia Lynn