Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs
© Blom et al; licensee BioMed Central Ltd. 2009
Received: 20 April 2009
Accepted: 1 December 2009
Published: 1 December 2009
Genome-wide linkage studies for Alzheimer's disease have implicated several chromosomal regions as potential loci for susceptibility genes.
In the present study, we have combined a selection of affected relative pairs (ARPs) from the UK and the USA included in a previous linkage study by Myers et al. (Am J Med Genet, 2002), with ARPs from Sweden and Washington University. In this total sample collection of 397 ARPs, we have analyzed linkage to chromosomes 1, 9, 10, 12, 19 and 21, implicated in the previous scan.
The analysis revealed that linkage to chromosome 19q13 close to the APOE locus increased considerably as compared to the earlier scan. However, linkage to chromosome 10q21, which provided the strongest linkage in the previous scan could not be detected.
The present investigation provides yet further evidence that 19q13 is the only chromosomal region consistently linked to Alzheimer's disease.
Alzheimer's disease (AD) is the most common form of dementia and the number of affected individuals rises dramatically with an aging population. Age is the most prominent risk factor, but genetics is also important for the risk of developing AD. Three genes are known to cause autosomal dominant early-onset AD: the amyloid beta precursor protein (APP) on chromosome 21 , presenilin 1 (PSEN1) on chromosome 14  and presenilin 2 (PSEN2) on chromosome 1 . For the much more common sporadic AD with later onset, apolipoprotein E (APOE) on chromosome 19q13 is so far the only identified susceptibility gene with consistently demonstrated association .
The ε4 allele of APOE is estimated to account for less than a third of the lifetime risk for AD [5, 6] and simulation studies have predicted at least four additional genetic loci contributing to age at onset . Although such calculations are by necessity based on certain assumptions, they support the possibility that there are more genetic susceptibility factors for AD to be identified. Genome-wide linkage studies using affected sib-pairs or families have implicated a number of chromosomal loci to hold susceptibility genes [8–14]. Regions on chromosomes 9, 10, 12 and 19 seem to be the most replicated, although the exact position of the peaks can differ substantially.
In the present study, we have combined a selection of affected relative pairs (ARPs) from the UK and the USA included in an earlier linkage study by Myers et al. . We have modified the original sample collection by excluding the NIMH sample and samples with ambiguous phenotypes, as well as by adding sample collections from Sweden and Washington University. We have analyzed linkage to regions on chromosomes 1, 9, 10, 12, 19 and 21, previously implicated in the study by Myers et al.
AAO ± SD
69.1 ± 6.2
75.0 ± 5.9
72.6 ± 6.1
72.4 ± 5.5
The ARPs were selected from families where at least one relative pair was diagnosed with possible, probable or definite AD according to NINCDS-ADRDA diagnostic criteria . All available family members, including unaffected relatives, were sampled and genotyped after informed consent had been collected from each participating individual or next of kin. Only Caucasian families were included to reduce potential genetic heterogeneity. This study was approved by local and national ethics committees.
Samples from the UK and the Indiana Alzheimer Disease Center National Cell Repository were also included in the study by Myers et al. To improve power of the present study, samples with ambiguous phenotypes were removed and new samples were added. This resulted in a total of 244 affected individuals from the UK and USA samples (129 ARPs) that were also genotyped in the study by Myers et al. but with another microsatellite marker set. Twelve of the families from Sweden were analyzed in Giedraitis et al. 2006 . There is also a likely overlap with the Swedish samples used in the present study and the sample collection used by Sillén et al. [13, 14], but the extent of this overlap is unknown to us.
Microsatellite marker information
Number of microsatellite markers
Average intermarker distance (cM)
Genotyping success rate (%)
Amplification of the microsatellite markers was performed by multiplex PCR and the resulting fragments were separated according to size on an ABI PRISM 3700 (Applied Biosystems, Foster City, CA, USA). For quality control, each run included two CEPH samples (1331-01 and 1331-02)  and two water samples.
The Genotyper software v3.7 (Applied Biosystems) was used for allele calling. Marker order and intermarker distances were obtained from the Marshfield reference map . APOE genotyping was performed at the respective research center.
Family structures were verified through the Graphical relationship representation software (GRR) . Mendelian errors were identified and allele frequencies for selected microsatellite markers were calculated including all available individuals using the MENDEL v8.0 software . Allele frequencies were calculated for the total sample as well as for each of the analyzed subgroups: SWE, UK USA, APOE ε4+ (ARPs where both individuals have at least one APOE ε4 allele), and APOE ε4- (ARPs where neither individual has an APOE ε4 allele). File conversion was performed using Mega v4.0 .
Allele sharing multipoint LOD scores (MLS) and two-point LOD scores (TLS) were calculated for all groups using the Allegro v2.0 software . As suggested by the software authors, an exponential model with scoring function Spairs and family weighting option "power: 0.5" was used. Significance levels of detected MLSs in the total sample and the analyzed subgroups were simulated through 1000 replications using the actual data set from the selected chromosomes.
In order to ensure high quality of the data included in the analysis, the GRR program was used on all available genotypes, including data from 270 microsatellite markers. This prompted us to exclude samples which displayed deviations from the expected average allele sharing between sibs or other family members. Having performed this quality check, 580 affected individuals from 261 pedigrees remained and were included in the analyses (Table 1).
The focus of this study was to further explore previously implicated linkage peaks from a genome scan by Myers et al. . Both studies include samples from the UK and USA, whereas the NIMH sample used in Myers et al. was not included in the present scan, and samples from Sweden and Washington University were added. Using this modified sample collection, linkage to chromosomes 1, 9, 10, 12, 19 and 21 was analyzed in the whole sample and in subgroups based on sample origin or APOE ε4 status.
Maximum MLS and (TLS) ≥1 from the present study
Nearest marker (cM)
Using data from the selected chromosomes, significance threshold levels were simulated for the total samples, as well as for the respective subgroups. After this simulation, linkage to chromosomes 19q13 in the total sample and the APOE ε4+ subgroup and to 1p36 in the UK subgroup are considered significant according to the definition by Lander and Kruglyak  (Table 3).
In the past decade there have been a number of attempts at identifying AD linkage regions using affected sib-pairs or extended families [8–14]. Although results have varied considerably and have sometimes been difficult to replicate, the most convincing linkage peaks have been reported from chromosomes 9, 10, 12, and 19.
In the present study, linkage peaks on chromosomes 1, 9, 10, 12, 19 and 21, previously implicated in a whole genome scan by Myers et al. have been further analyzed using a modified version of the original sample with an added collection of ARPs from Sweden and Washington University. We could detect significant linkage to chromosome 19q13 in the immediate vicinity of the APOE locus. This linkage peak was noticeably increased from the scan by Myers et al. and the Swedish sample contributed considerably to the improved linkage (Table 3). The influence of the APOE locus on AD has been correlated to a lower age at onset [4, 24], as further demonstrated in our recent analysis of the chromosome 19 linkage . Accordingly, linkage analysis of the NIMH cohort by Blacker et al. demonstrated the highest linkage to chromosome 19q13 in their subsample with earlier disease onset, whereas no linkage to this region was detected in their late onset sample . The only other significant linkage found in the present study was to chromosome 1p36 in the UK subsample. However, this peak was neither detected in the other subgroups, nor in the total sample.
In the original whole genome scan by Myers et al., the most significant linkage peak was demonstrated on chromosome 10q21 (82 cM) in the whole sample. Blacker et al. also found linkage in the region, to chromosome 10q22 (92 cM) in their total collection of NIMH samples. In the present study, we could not detect linkage to chromosome 10q21, even though a suggestive linkage of MLS 1.8 was detected to chromosome 10q22 (105 cM) in the APOE ε4- sample. Although the sample size in the present study is smaller than in the study by Myers et al. (380 and 451 ASPs, respectively), the previous study by Kehoe et al.  using 292 ASPs and including overlapping samples with the Myers study also detected linkage to chromosome 10q21. This suggests that the absence of a linkage peak on chromosome 10q21 in the present study might be due to sample differences between the studies rather than sample size. However, we cannot completely exclude that our linkage to chromosome 10q22 in the APOE ε4- subsample coincides with the previously detected linkage to chromosome 10q21-22, although the positions of these peaks differ by 13-23 cM. Certain caution is also called for as the APOE ε4- subsample is rather limited in size (42 ARPs).
Inconsistent results between linkage studies might reflect heterogeneity in sample cohorts, including age at onset, ethnic background and diagnostic criteria. Our finding of significant linkage to chromosome 19q13, but to no other regions in the total sample in combination with the results presented by Blacker et al., suggests that finding significant linkage to both chromosome 19q13 and additional regions in the same sample is uncommon.
In the past few years, whole genome association studies have successfully identified susceptibility loci for a number of complex conditions. However, APOE is so far the only locus demonstrating strong association to AD [26–28]. Sample sizes have turned out to be crucial and sample collections including thousands of cases have been analyzed for association . Increasing the number of samples in analyses also of ARPs would most likely be beneficial for the outcome and therefore further efforts to combine different sample collections should be made. It has been suggested that data from linkage analysis of affected sib-pairs could also be used to verify candidate susceptibility genes from association studies, since the frequency of a risk allele is expected to be higher in siblings sharing the locus than in population based cases .
In this linkage study, we have analyzed a sample collection of AD ARPs from Sweden, the UK and the USA for linkage to chromosomes 1, 9, 10, 12, 19 and 21, implicated in the previous study by Myers et al. . The highest linkage was detected on chromosome 19q13 close to the APOE gene. This linkage was extensively contributed by the Swedish samples, which has a lower average age at onset than the other subgroups. There was no evidence of the previously demonstrated linkage to chromosome 10q21 in the whole sample collection, and the relevance of the suggestive linkage within the APOE ε4- subgroup to chromosome 10q22 is somewhat uncertain due to the altered position of the peak and the restriction to this subgroup only. Our study demonstrates that chromosome 19q13 including APOE, at this point, is the only consistently linked locus for AD. This is also supported by genome wide association studies, demonstrating that APOE is the major susceptibility gene for AD . Any additional susceptibility loci for AD are therefore likely to have much smaller effects, demanding very large sample sizes for detection.
The authors wish to thank all the participating families and everyone involved in collecting samples. The Swedish work was supported by The Swedish Research Council, The Swedish Alzheimer foundation, APOPIS (Contract No. LSHM-CT-2003-503330), and NIH grant number R01 AG08724. The UK group was supported by funding from the Alzheimer's Research Trust and the Medical Research Council. The USA samples were collected with support from the NIA/NIH intramural research program and grants numbers U01 MH46281, U01 MH46290, U01 MH46373 (NIMH), U24 AG21886 (NCRAD), and AG16208 (AG).
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