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. Author manuscript; available in PMC: 2011 May 9.
Published in final edited form as: Crit Care Med. 2007 Jan;35(1):48–56. doi: 10.1097/01.CCM.0000251132.10689.F3

Table 5.

Haplotype frequencies for the mannose binding lectin-2 (MBL-2) codon 52, 54, and 57 and MBLXY polymorphisms and development of acute respiratory distress syndrome (ARDS) and 60-day mortality in ARDS

Development of ARDS
Mortality in ARDS
Patients With ARDS with Genotype/Total No. of Patients with Genotype (%)
Nonsurvivors with Genotype/All ARDS Patients with Genotype (%)
No. of Copies of Haplotype
No. of Copies of Haplotype
Haplotypea Haplotype Frequencyb 0 1 2 p Value 0 1 2 p Value
AAAY 0.59 42/107 (39) 88/285 (30) 62/197 (31) .2 20/42 (48) 41/86 (48) 24/62 (39) .5
AAAX 0.16 124/406 (31) 55/158 (35) 11/25 (44) .3 54/124 (44) 27/55 (49) 4/11 (36) .7
DAAY 0.09 165/496 (33) 25/91 (27) 0/2 (0) .4 70/165 (42) 15/25 (60) 0 .1
ABAY 0.14 134/422 (32) 49/157 (31) 7/10 (70) <.05 63/134 (47) 16/49 (33) 6/7 (86) .02
AACY 0.02 185/571 (32) 5/17 (29) 0/1 (0) >.9 82/185 (44) 3/5 (60) 0 .7
a

Haplotypes consist of codon 52, codon 54, codon 57, and MBLXY. The variant alleles for codon 52, 54, and 57 are D, B, and C, respectively. The wild-type allele is known collectively as the A allele

b

haplotype frequency among controls only. The p values from Fisher’s exact test for each haplotype are presented. Only the ABAY haplotype was associated with development of ARDS (p < .05) and mortality in ARDS (p = .02).