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Includes letter from Ed Yazbak, MD!
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SCIENCE
Scientists Debate Latest MMR - Vax Study: BMJ Letters
Measles, mumps, and rubella (MMR) vaccine and autism
http://bmj.com/cgi/content/full/323/7305/163?view=full&pmid=11463692
BMJ 2001;323:163 ( 21 July ) For abstract of study being debated:
http://bmj.com/cgi/content/abstract/322/7284/460
Letters: * Ecological studies cannot answer main question
·
Argument is too simplistic
·
MMR cannot be exonerated without explaining increased incidence
of autism
·
Authors reply
Ecological Studies Cannot Answer Main Question
EDITOR
Kaye et al undertook an ecological study comparing the
time trend in measles, mumps, and rubella (MMR) vaccine coverage with the time
trend in diagnoses of autism.1 They found a marked increase in the incidence of
codes for autism in childrens electronic general practice records over 11
years.
We agree with their conclusion that MMR cannot be the
cause of this observed increase since the vaccine coverage remained constant
over the same time. There have been changes in the classification of autistic
diseases and in the likelihood of case ascertainment in recent years, and a
more rigorous review of cases may clarify whether some of the increase was due
to alterations in diagnostic practice.2 Only 81% of cases were reported to have
been referred to a specialist, raising questions about the validity of the diagnoses
used by Kaye et al. Children with medical conditions present from birth and
known to be associated with an increased risk of autism (fragile X disorder,
tuberous sclerosis, phenylketonuria, and congenital rubella) were not excluded.
The failure to find an association between the time trends
in vaccine coverage and the incidence of autism codes in childrens electronic
general practice records does not exclude a causal association. Whether
exposure to MMR vaccination increases the risk of autism is of great public
health importance and can be usefully investigated using the general practice research
database. We have been funded by the United Kingdom Medical Research Council to
undertake an investigation of the causes of autism, including an assessment of
the potential role of MMR vaccine using case-control and case series
approaches.
The electronic general practice records in the database
will be supplemented by a full record review of all cases and, subject to
ethical approval, questionnaires to parents of both affected children and
controls.
We will undertake a detailed validation and classification
of all cases and
establish the date of onset of symptoms. In addition, we
will obtain
information on potential confounding factors from both cases
and controls. A
detailed protocol of our study has been published.3
Liam Smeeth, clinical research fellow, department of
epidemiology and population health.
liam.smeeth@lshtm.ac.uk
Andrew J Hall, head, infectious disease epidemiology unit. Laura C Rodrigues, reader in epidemiology,
department of infectious and tropical diseases.
Xiangning Huang, research fellow, department of infectious
and tropical diseases.
Peter G Smith, head, department of infectious and tropical
diseases.
London School of Hygiene and Tropical Medicine,
London WC1E 7HT
Eric Fombonne, reader in epidemiological child psychiatry.
Institute of Psychiatry, Kings College London, Department
of Child
and Adolescent Psychiatry, Medical Research Council Child
Psychiatry Unit,
London SE5 8AF
1. Kaye JA, del Mar
Melero-Montes M. Mumps, measles, and rubella vaccine and the incidence of
autism recorded by general practitioners: a time trend analysis. BMJ 2001; 322:
460-463[Abstract/Full Text]. (24 February.)
2. Fombonne E. Is there
an epidemic of autism? Pediatrics 2001; 107:
411-413[Full Text].
3. Smeeth L, Hall AJ,
Fombonne E, Rodrigues LC, Huang X, Smith PG. A case-control study of autism and
mumps-measles-rubella vaccination using the general practice research database:
design and methodology. BMC Public
Health 2001; 1: 2[Medline].
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* * *
Argument Is Too Simplistic
EDITOR
Kaye et al analysed time trends in measles, mumps, and
rubella (MMR) vaccine and the incidence of autism.1 Because the increase of
autism is gradual whereas the prevalence of immunisation is constant, they
argue that there is no evidence of an association. This argument, however,
rests on the assumption that the rate of diagnosis rate each year after the
onset of clinical symptoms is constant with respect to birth cohort and that a
mild case has a constant chance of being diagnosed.
Altmann points out that 40% of cases have diagnosis
delayed up to three years.2 Could increasing awareness of paediatricians and
general clinicians of autism during this period account for the gradual
increase? When the first unexpected
extra cases were found in 1991-2, could that not have increased vigilance? As
evidence, we point to the median age at diagnosis as reported by the authors.
Except for 1993, there seems to be a trend towards earlier
diagnosis. We exclude 1998-9 because
the cohort then changed substantially, with several practices no longer
providing information. Could Kaye et al show a test of trend from 1988 to 1997
to see whether there was a systematic decrease in age at diagnosis? Is it also
possible to investigate the notion that average severity of cases was dropping
over this time period?
Finally, was there a trend towards earlier vaccination, as
can be seen in data from California?3 For example, did the percentage of
vaccinations at less than 10 months increase over time?
We submit that the argument given by Kaye et al is too
simplistic to
reassure us that there is no link between MMR and autism.
The current
arguments in favour of the link, however, remain
unconvincing. 4 5
Michael Edwardes, research fellow.
Division of Clinical Epidemiology, Ross 4.06, Royal Victoria
Hospital, 687
Pine Avenue West, Montreal, Province of Quebec, Canada H3A
1A1
michael.edwardes@clinepi.mcgill.ca
Marc Baltzan, consultant physician.
Mount-Sinai Hospital, 5690 Cavendish, Cote-St-Luc, Montreal,
Province of
Quebec, Canada H4W 1S7
1. Kaye JA, del Mar Melero-Montes
M. Mumps, measles, and rubella vaccine and the incidence of autism recorded by
general practitioners: a time trend analysis. BMJ 2001; 322:
460-463[Abstract/Full Text]. (24 February.)
2. Altmann D. Autism
and measles, mumps and rubella vaccine. Lancet 2000;
355: 409[Medline].
3. Dales L, Hammer SJ,
Smith NJ. Time trends in autism and in MMR immunization coverage in California.
JAMA 2001; 285: 1183-1185[Medline].
4. Wakefield AJ, Murch
SH, Anthony A, Linell J, Casson DM, Malik M, et al. Ileal-lymphoid-nodular
hyperplasia, non-specific colitis and pervasive developmental disorder in
children. Lancet 1998; 351:
637-641[Medline].
5. Wakefield AJ. MMR
vaccination and autism. Lancet 1999; 354:
949-950[Medline].
* * *
MMR Cannot Be Exonerated Without Explaining Increased
Incidence Of Autism
EDITOR
Kaye et al observe that the rise in the incidence of
autism cannot be
attributed to measles, mumps, and rubella (MMR) vaccine
because vaccination
remained consistently above 90% in the period studied.1
I have several issues with their study:
(1) The cohort of
children chosen was born during 1988-93. MMR was introduced in the United
Kingdom in 1988 and an uptake of 90-95% is unlikely to have been achieved from
the first year.
(2) Kaye et al
effectively excluded children born before 1988 who may have been vaccinated in
or after 1988.
(3) The 114 boys
selected were observed until the age of 71 months.
Many of them could have succumbed after the second MMR
vaccination (booster), which is given between the ages of 4 and 5 years. The
study did not mention how many children received two MMR vaccinations.
(4) MMR vaccine was
previously given alone at 15 months or later. Then the age was lowered to 12-14
months and other vaccines were administered concomitantly, increasing the
immune antigenic insult at a younger more susceptible age and effectively
increasing the incidence of autism.
(5) The restriction of
the cases in the main analysis to 114 boys is of concern. A breakdown of the
290 children in the 1990-9 birth cohorts by sex and year of birth would have
been informative. A larger proportion of girls among the 176 cases excluded
might have been relevant to the completeness of the autism figures.
(6) The fact that
neither DSM-IV nor IC-10 was systematically used in the United Kingdom creates
further doubts about the significance of the findings.
Professor Brent Taylor in the Lancet (1999;353:2026-9) and
now Kaye et al have clearly documented the epidemic of autism in the United
Kingdom. Before 1988 the incidence of
autism was 1 in 10 000; after 1988 the year MMR was introduced it leapt to 8 in
10 000. By 1993 it was 29 in 10 000.
Kaye et al cannot exonerate MMR without offering a
reasonable explanation for the increase.
Until safety studies on MMR are independent of drug
companies and are large scale and comprehensive, and until researchers review
with parents the documented adverse reactions of bowel disease and autism, the
triple jab remains suspect.
F Edward Yazbak, doctor.
TL Autism Research, 70 Viewcrest Drive, Falmouth, MA
02540, USA
1. Kaye JA, del Mar
Melero-Montes M. Mumps, measles, and rubella vaccine and the incidence of
autism recorded by general practitioners: a time trend analysis. BMJ 2001; 322:
460-463[Abstract/Full Text]. (24 February.)
* * *
Authors Reply
EDITOR
We disagree with Smeeth et al applying the term ecological
to our study of measles, mumps, and rubella (MMR) vaccine and autism. In an ecological
study the units of analysis are populations or groups of people.1 But our study
focused on individual children diagnosed with autism (although we also reported
the prevalence of exposure to MMR for all children in the general practice
research database who were born in 1988-93).
It is unimportant that we included a few children with
conditions predisposing to autism because we were evaluating the relation
between MMR vaccination and the risk of being diagnosed with autism per se. We
agree that more work is needed to evaluate possible causes of the recent
increase in autism other than the MMR vaccine.
A non-parametric test (extension of Wilcoxon rank sum test
in Stata, version 7.0) provides no evidence for a trend toward lower age at
diagnosis over time for the 305 cases diagnosed in 1988-99 (P=0.88), even
including only cases diagnosed before 1998 (p=0.61). We doubt that lower age at
diagnosis explains the nearly fourfold increase in risk for two to five year olds
in the 1988-93 birth cohorts.
The median age at first MMR in the base population was 15
months for the 1988 birth cohort, 14 months for the 1989-1996 cohorts, and 13
months for the 1997 cohort. Small differences in age at first MMR are unlikely
to account for the large change in the observed risk of autism diagnosed at age
2-5. We agree that changing diagnostic criteria (for example, diagnosing milder
cases) may be one explanation for the increase in diagnosed autism.
We did not include only classic cases. We restricted our
main analysis to boys to maximise risk estimate precision since girls make up
only about a fifth of the diagnosed cases. We focused on children aged 2-5, in
whom the incidence of diagnosed autism is greatest. We analysed 1988-93 birth
cohorts to have enough follow up information to calculate four year risk (age
2-5). Using a different upper limit for
age at diagnosis in some birth cohorts would impair the comparability of risk
among the cohorts.
MMR was introduced in the United Kingdom in 1988 and is
first administered around the age of 15 months. Children born in 1988 were vaccinated
in 1989 or 1990, so our data do not suggest that uptake of 95% was achieved
from the first year. Excluding cases born before 1988 has no effect on risk
estimates for the birth cohorts we reported or on the relation between MMR
vaccine and diagnosed autism in these cohorts.
Only 12/114 boys in our main analysis received more than
one MMR vaccination before their first recorded diagnosis of autism too few to separately
estimate risk for two vaccinations compared with one. We did not study whether
vaccines other than MMR are associated with the increasing incidence of autism.
James A Kaye, epidemiologist.
Maria del Mar Melero-Montes, epidemiologist.
Hershel Jick, associate professor of medicine.
Boston Collaborative Drug Surveillance Program, Boston
University School of
Medicine, 11 Muzzey Street,
Lexington, MA 02421, USA
Lenny Schafer, Editor Catherine Johnson PhD
Ron Sleith Kay Stammers
Editor@feat.org Edward Decelie CALENDAR: Michelle Guppy events@feat.org
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