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. 2015 Oct;24(5):862-71.
doi: 10.1007/s10897-015-9822-z. Epub 2015 Feb 3.

Do Attachment Style and Emotion Regulation Strategies Indicate Distress in Predictive Testing?

Affiliations

Do Attachment Style and Emotion Regulation Strategies Indicate Distress in Predictive Testing?

Lucienne B van der Meer et al. J Genet Couns. 2015 Oct.

Abstract

Predictive genetic testing for a neurogenetic disorder evokes strong emotions, and may lead to distress. The aim of this study is to investigate whether attachment style and emotion regulation strategies are associated with distress in persons who present for predictive testing for a neurogenetic disorder, and whether these psychological traits predict distress after receiving test results. Self-report scales were used to assess attachment insecurity (anxiety and avoidance) and maladaptive emotion regulation strategies (self-blame, rumination, catastrophizing) in adults at 50 % risk for Huntington's Disease (HD), Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL), and Hereditary Cerebral Hemorrhage With Amyloidosis - Dutch type (HCHWA-D), when they presented for predictive testing. Distress was measured before testing and twice (within 2 months and between 6 and 8 months) after receiving test results. Pearson correlations and linear regression were used to analyze whether attachment style and emotion regulation strategies indicated distress. In 98 persons at risk for HD, CADASIL, or HCHWA-D, attachment anxiety and catastrophizing were associated with distress before predictive testing. Attachment anxiety predicted distress up to 2 months after testing. Clinicians may consider looking for signs of attachment anxiety and catastrophizing in persons who present for predictive testing, to see who may be vulnerable for distress during and after testing.

Keywords: Attachment style; CADASIL; Distress; Emotion regulation strategies; HCHWA-D; Huntington’s disease; Neurogenetic disorders; Predictive testing.

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Conflict of interest statement

Lucienne van der Meer, Erik van Duijn, Erik Giltay, and Aad Tibben declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Flowchart of participants. Baseline = baseline assessment, prior to receiving DNA test results. T1 = first follow-up assessment; median 16 days after receiving DNA test results. T2 = second follow-up assessment; median 193 days after receiving DNA test results
Fig. 2
Fig. 2
Distress scores of participants with negative or positive test result (Huntington’s Disease, CADASIL and HCHWA-D). CADASIL = Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. HCHWA-D = Hereditary Cerebral Haemorrhages with Amyloidosis - Dutch type. The BSI scores are depicted on a logarithmic scale because of its positively skewed distribution. Differences between the two groups per time point are tested using a t-test for independent samples

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