An alcohol dehydrogenase 7 gene polymorphism associates with both acute and chronic pain in sickle cell disease

Author:

Kashyap Yavnika1,He Ying12,Sadhu Nilanjana1,Yao Yingwei3,Wilkie Diana J3,Molokie Robert E1245,Wang Zaijie Jim1267

Affiliation:

1. Department of Pharmaceutical Sciences, University of Illinois College of Pharmacy, Chicago, IL 60612, USA

2. Comprehensive Sickle Cell Center, University of Illinois Chicago, Chicago, IL 60612, USA

3. Department of Biobehavioral Nursing Science, University of Florida College of Nursing, Gainesville, FL 32610, USA

4. Jesse Brown Veteran's Administration Medical Center, Chicago, IL 60612, USA

5. Division of Hematology/Oncology, University of Illinois College of Medicine, Chicago, IL 60612, USA

6. Department of Neurology & Rehabilitation, University of Illinois College of Medicine, Chicago, IL 60612, USA

7. Department of Biomedical Engineering, University of Illinois Chicago College of Engineering, Chicago, IL 60607, USA

Abstract

Introduction: As the most distressing complication of sickle cell disease (SCD), pain is marked by considerable heterogenicity. In this study we explored the potential association of alcohol dehydrogenase 7 gene ( ADH7) polymorphism rs971074 with sickle cell pain. Methods: We analyzed clinical phenotypes and the rs971074 single-nucleotide polymorphism in ADH7 by MassARRAY-iPlex analysis in a cohort of SCD patients. Results: The synonymous rs971074 was significantly associated with both acute and chronic pain in SCD. Patients with the minor T allele(s) recorded significantly more crisis episodes and severe chronic pain symptoms. Conclusion: Our study has identified the rs971074 minor T allele as a genetic biomarker potentially influencing acute and chronic pain. These findings may ultimately help inform strategies to develop precision pain therapies in SCD.

Funder

National Heart, Lung, and Blood Institute

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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