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. Author manuscript; available in PMC: 2008 Sep 15.
Published in final edited form as: Clin Gastroenterol Hepatol. 2008 Feb 7;6(3):333–338. doi: 10.1016/j.cgh.2007.12.014

Table 1. Characteristics of the Study Population (N=174) and Univariate Analysis of Factors Predicting Disclosure of Genetic Test Results to Any Family Members Beyond 1st Degree.

All Subjects who had Genetic Testing
(N=174)
Subject Disclosure to Family Members

Told Beyond 1st Degree
(N=109)*
Did Not Tell Beyond 1st Degree
(N=53)*
Frequency (%) Frequency (%) Frequency (%) p-value
Mean Age (Range) 46.7 (18-79) 45.96 45.26 0.73
Gender 0.20
 Male 52 (29.9) 28 (59.6) 19 (40.4)
 Female 122 (70.1) 81 (70.4) 34 (29.6)
Race 0.15
 White 157 (90.8) 96 (65.3) 51 (34.7)
 Non-white 16 (9.3) 13 (86.7) 2 (13.3)
 Unknown/missing 1 (--)
Education 0.72
 Less than college grad 53 (31.0) 34 (69.4) 15 (30.6)
 At least college grad 118 (69.0) 73 (65.8) 38 (34.2)
 Unknown/missing 3 (--) 2 (--) -- (--)
Marital Status 1.00
 Married 132 (75.9) 81 (66.9) 40 (33.1)
 Not Married 38 (21.8) 26 (68.4) 12 (31.6)
 Unknown/missing 4 (2.3) 2 (--) 1 (--)
Cancer Diagnosis 0.50
 Yes 106 (60.9) 66 (69.5) 29 (30.5)
 No 68 (39.1) 43 (64.2) 24 (35.8)
Test Results 0.03
 Positive 104 (59.8) 73 (75.3) 24 (24.7)
 Indeterminate 47 (27.0) 24 (57.1) 18 (42.9)
 True negative 23 (13.2) 12 (52.2) 11 (47.8)
Cancer Worry 0.55
 Low 58 (33.5) 35 (66.0) 18 (34.0)
 Moderate 65 (37.6) 44 (72.1) 17 (27.9)
 High 50 (28.9) 30 (62.5) 18 (37.5)
 Unknown/missing 1 (--)
Prior Genetic Testing in Family 1.00
 Yes 128 (73.6) 82 (67.2) 40 (32.8)
 No 39 (22.4) 24 (68.6) 11 (31.4)
 Don't Know 7 (4.0) 3 (--) 2 (--)
Mutation Previously identified in Family 0.48
 Yes 113 (64.9) 75 (69.4) 33 (30.6)
 No 61 (35.1) 34 (63.0) 20 (37.0)
History of Lynch Syndrome cancer in 1 or more relatives 1.00
 Yes 155 (89.1) 98 (67.1) 48 (32.9)
 No 19 (10.9) 11 (68.8) 5 (31.2)
Mean number of relatives with Lynch Syndrome Cancers 3.71 [+/- 2.0] 4.04 [+/- 2.1] 3.38 [+/- 1.8] 0.05
Subjects With Children 0.72
 Yes 122 (70.1) 76 (68.5) 35 (31.5)
 No 52 (29.9) 33 (64.7) 18 (35.3)
Ever evaluated in a genetics/ high risk clinic 0.78
 Yes 154 (89.0) 98 (67.6) 47 (32.4)
 No 19 (11.0) 10 (62.5) 6 (37.5)
 Unknown/missing 1 (--) 1 (--) -- (--)
*

162 Subjects who indicated they have at least 1 SDR or TDR to tell

Comparison between subjects who did and did not tell relatives beyond 1st degree, Fisher's Exact Test used for all categorical variables; t-test used for all continuous variables