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Letter to the Editor
Published Online: 1 March 2002

Seasonal Fluctuation in Schizophrenia

Publication: American Journal of Psychiatry
To the Editor: Jaana M. Suvisaari, M.D., Ph.D., and her colleagues suggested in their intriguing article (1) that procreation in the summertime represents a constant hazard, in addition to an irregular environmental risk factor, for schizophrenia. Are these two components independent variables or just two facets of a common pathogenic mechanism that might ultimately be preventable?
Using a novel climatic data set (2, 3), we compared their data with mean temperature and precipitation rates over the same time. The dramatic multiyear fluctuations, particularly the odds amplitude for patients born in 1955–1959, cannot be explained by the subtle climatic variations, neither in the more densely populated southern part nor in the rest of Finland. The fluctuations in schizophrenia births, which have also been reported from Denmark and Scotland (4), might rather be related to an additional stochastic factor prevalent in the north.
In comparison to the first account by Tramer (5), the reported data, showing the lower schizophrenic birth rates in July through August (1955–1959), reveal another potential clue to the environmental determinant of schizophrenia. In Switzerland, we have, in addition to the widely replicated excess of schizophrenia births in the winter and spring months, a second minor peak in July (5). This bimodal distribution mirrors the seasonal concentration of ticks (Ixodes ricinus) 9 months earlier, with a major peak in spring and a minor peak in autumn separated by a decrease in humidity in the summer (6). Ticks containing Borrelia burgdorferi are prevalent in the urban recreational areas of Helsinki. However, as in the Alps, the minimal mean temperature of 7°C required for tick activity (6) allows only one peak from May to September in Finland, during which time the annual precipitation is also highest. Tick activity coinciding with procreational preference in the summertime might thus represent the stable component. While a few autumn-feeding I. ricinus ticks are still active up to November in central Europe (6), the temperature falls below 0°C in Finland. Adverse weather conditions, known to underlie the stochastic year-to-year oscillations of tick populations (7, 8), might thus reflect the irregular component of schizophrenia births in the north.
Contrary to the current belief shared by Dr. Suvisaari et al. and others, neither the excess of schizophrenia winter births nor the excess of schizophrenia itself occurs at a constant rate worldwide. South of the Wallace line (9, 10), which limits the southward spread of species, including B. burgdorferi-transmitting ticks (6), seasonal schizophrenia trends appear to be insignificant or nonexistent, and in certain remote areas schizophrenia is even absent (11). We found only one psychotic patient in a neuropsychiatric survey comprising over 10,000 Papuans in the interior of New Guinea—fewer than expected (12). In Australia, where Borrelia garini is only sporadically introduced by migratory seabirds, B. burgdorferi could not be detected and cannot be transmitted by the local tick, I. holocyclus. It is not surprising after all that the higher rates of schizophrenia have been reported from the northeastern, northwestern, and Great Lakes states, which score the highest numbers of Ixoid tick populations and infections by B. burgdorferi(13).
An early prenatal event interfering with neuronal migration has been suggested to underlie the consistent pattern of cellular disarray observed in schizophrenia brains. This hypothesis, however, contrasts with the reported pregnancy and birth complications during the second and third trimesters related to hypoxic damage or viral infections, as suggested by Dr. Suvisaari et al. and others. However, since B. burgdorferi has direct access to host genes, which the intracellular pathogen exploits like a virus for its own replication, a novel mutation might thus affect a gene prone to be hit by B. burgdorferi, the cannabinoid receptor gene (14), which is known to induce both hypoxic resistance and neuronal migration.

References

1.
Suvisaari JM, Kaukka JK, Lönnqvist JK: Season of birth among patients with schizophrenia and their siblings: evidence for the procreational habits hypothesis. Am J Psychiatry 2001; 158:754-757
2.
New M, Hulme M, Jones P: Representing twentieth-century space time climate variability, part I: development of a 1961-90 mean monthly terrestrial climatology. J Climate 1999; 12:829-856
3.
New M, Hulme M, Jones P: Representing twentieth-century space time climate variability, part II: development of 1901-96 monthly grids of terrestrial surface climate. J Climate 2000; 13:2217-2238
4.
Adams W, Kendell RE: Annual variation in birth rate of people who subsequently develop schizophrenia. Br J Psychiatry 1999; 175:522-527
5.
Tramer M: Ueber die biologische Bedeutung des Geburtsmonates, insbesonderer für die Psychoseerkrankungen. Schwiez Arch Neurol Psychatr 1929; 24:17-24
6.
Sonenshine DE: Biology of Ticks. New York, Oxford University Press, 1989
7.
Korotkov IuS: [Cyclic processes in the dynamics of the population count of the taiga tick and their relation to weather and climatic conditions.] Parazitologiia 1998; 32:21-31(Russian)
8.
Talleklint L, Jaenson TG: Seasonal variations in density of questing Ixodes rininus (Acari: Ixodidae) nymphs and prevalence of infection with B. burgdorferi s.l. in south central Sweden. J Med Entomol 1996; 33:592-597
9.
McGrath JJ, Welham JL: Season of birth and schizophrenia: a systematic review and meta-analysis of data from the Southern Hemisphere. Schizophr Res 1999; 35:237-242
10.
Torrey EF, Miller J, Rawlings R, Yolken RH: Seasonality of births in schizophrenia and bipolar disorder: a review of the literature. Schizophr Res 1997; 28:1-38
11.
Dohan FC, Harper EH, Clark MH, Rodrigue RB, Zigas V: Is schizophrenia rare if grain is rare? Biol Psychiatry 1984; 19:385-399
12.
Fritzsche M, Gottstein B, Wigglesworth MC, Eckert J: Serological survey of human cysticercosis in Irianese refugee camps in Papua New Guinea. Acta Trop 1990; 47:69-77
13.
Brown JS Jr: Geographic correlation of schizophrenia to ticks and tick-borne encephalitis. Schizophr Bull 1994; 20:755-775
14.
Fritzsche M: Are cannabinoid receptor knockout mice animal models for schizophrenia? Med Hypotheses 2001; 56:638-643

Information & Authors

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Go to American Journal of Psychiatry
Go to American Journal of Psychiatry
American Journal of Psychiatry
Pages: 499-a - 500

History

Published online: 1 March 2002
Published in print: March 2002

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MARKUS FRITZSCHE, M.D.
Adliswil, Switzerland
JÜRG SCHMIDLI, PH.D.
Zurich, Switzerland

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