Investigator

Kari E. North

Vice President of Border Health, Director, Professor · University of Texas Health Sciences Center, Browsville campus, Epidemiology

About

KENKari E. North
Papers(1)
Extended Human Papill…
Collaborators(10)
Michael G. HudgensRachel L. MaguireRex C. BentleySusan K. MurphyWendy R. BrewsterAdriana C. VidalAlexandra BukowskiCathrine HoyoFidel ValeaJennifer S. Smith
Institutions(6)
University Of North C…North Carolina State …Duke UniversityCedars Sinai Medical …Virginia Department O…Unc Lineberger Compre…

Papers

Extended Human Papillomavirus Genotyping to Predict Progression to High-Grade Cervical Precancer: A Prospective Cohort Study in the Southeastern United States

Abstract Background: High-risk human papillomavirus (hrHPV) testing is utilized in primary cervical cancer screening, generally along with cytology, to triage abnormalities to colposcopy. Most screening-based hrHPV testing involves pooled detection of any hrHPV or of HPV16/18. Cervical neoplasia progression risks based on extended hrHPV genotyping—particularly non-16/18 hrHPV types—are not well characterized. HPV genotype-specific incidence of high-grade cervical intraepithelial neoplasia or more severe (CIN2+) following an abnormal screening result was examined. Methods: We assessed a US-based prospective, multiracial, clinical cohort of 343 colposcopy patients with normal histology (n = 226) or CIN1 (n = 117). Baseline cervical samples underwent HPV DNA genotyping, and participants were followed up to 5 years. Genotype-specific CIN2+ incidence rates (IR) were estimated with accelerated failure time models. Five-year CIN2+ risks were estimated nonparametrically for hierarchical hrHPV risk groups (HPV16; else HPV18/45; else HPV31/33/35/52/58; else HPV39/51/56/59/68). Results: At enrollment, median participant age was 30.1 years; most (63%) were hrHPV-positive. Over follow-up, 24 participants progressed to CIN2+ (7.0%). CIN2+ IR among hrHPV-positive participants was 3.4/1,000 person-months. CIN2+ IRs were highest for HPV16 (8.3), HPV33 (7.8), and HPV58 (4.9). Five-year CIN2+ risk was higher for HPV16 (0.34) compared with HPV18/45 (0.12), HPV31/33/35/52/58 (0.12), and HPV39/51/56/59/68 (0.16) (P = 0.05). Conclusions: Non-16/18 hrHPV types are associated with differential CIN2+ progression rates. HPV16, 33, and 58 exhibited the highest rates over 5 years. HPV risk groups warrant further investigation in diverse US populations. Impact: These novel data assessing extended HPV genotyping in a diverse clinical cohort can inform future directions to improve screening practices in the general population.

14Works
1Papers
11Collaborators
Genetic Predisposition to DiseaseCoronary DiseaseDisease ProgressionPeriodontitisCoronary Artery DiseaseEarly Detection of Cancer

Positions

2025–

Vice President of Border Health, Director, Professor

University of Texas Health Sciences Center, Browsville campus · Epidemiology

2025–

Researcher

University of North Carolina at Chapel Hill · Epidemiology

2014–

Professor

University of North Carolina at Chapel Hill · Department of Epidemiology and Carolina Center for

2007–

Associate Professor

University of North Carolina at Chapel Hill · Department of Epidemiology and Carolina Center for

2002–

Assistant Professor

University of North Carolina at Chapel Hill · Department of Epidemiology and Carolina Center for

2000–

Postdoctoral Scientist

Southwest Foundation for Biomedical Research · Department of Genetics

1997–

Senior Research Assistant

Southwest Foundation for Biomedical Research · Department of Genetics

1992–

Research Assistant

University of Kansas · Department of Pharmacology

1992–

Editorial Assistant

University of Kansas · Human Biology

1992–

Summer Fellow

National Institutes of Health · Animal Research Center

Education

2000

Doctor of Philosophy (with honors)

University of Kansas · Anthropological Genetics

1995

Masters of Arts

University of Kansas · Anthropological Genetics

1992

Bachelor of Arts (with honors)

University of South Florida · Anthropology

Country

US