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Patterns of co-occurring birth defects among infants with hypospadias.
Ludorf, Katherine L; Benjamin, Renata H; Navarro Sanchez, Maria Luisa; McLean, Scott D; Northrup, Hope; Mitchell, Laura E; Langlois, Peter H; Canfield, Mark A; Scheuerle, Angela E; Scott, Daryl A; Schaaf, Christian P; Ray, Joseph W; Oluwafemi, Omobola; Chen, Han; Swartz, Michael D; Lupo, Philip J; Agopian, A J.
Affiliation
  • Ludorf KL; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.
  • Benjamin RH; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.
  • Navarro Sanchez ML; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.
  • McLean SD; Clinical Genetics Section, The Children's Hospital of San Antonio, San Antonio, TX, USA.
  • Northrup H; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Mitchell LE; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.
  • Langlois PH; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA.
  • Canfield MA; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA.
  • Scheuerle AE; Department of Pediatrics, Division of Genetics and Metabolism, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
  • Schaaf CP; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA; Heidelberg University, Institute of Human Genetics, Heidelberg, Germany.
  • Ray JW; Department of Pediatrics, Division of Medical Genetics and Metabolism, University of Texas Medical Branch, Galveston, TX, USA.
  • Oluwafemi O; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA.
  • Chen H; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA; Center for Precision Health, UTHealth School of Public Health and UTHealth School of Biomedical Informatics, Houston, TX, USA.
  • Swartz MD; Department of Biostatistics and Data Science, UTHealth School of Public Health, Houston, TX, USA.
  • Lupo PJ; Department of Pediatrics, Section of Hematology-Oncology, Baylor College of Medicine, Houston, TX, USA.
  • Agopian AJ; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX, USA. Electronic address: a.j.agopian@uth.tmc.edu.
J Pediatr Urol ; 17(1): 64.e1-64.e8, 2021 02.
Article in En | MEDLINE | ID: mdl-33281045
ABSTRACT

INTRODUCTION:

Hypospadias, one of the most common male genital birth defects, occurs in 1 out of every 200 male births in the United States and is increasing in prevalence globally.

OBJECTIVE:

This study aimed to characterize the combinations of birth defects that co-occur with hypospadias more often than expected by chance, while accounting for the complex clustering patterns of congenital defects. STUDY

DESIGN:

We analyzed cases with hypospadias and at least one additional co-occurring defect from the Texas Birth Defect Registry born between 1999 and 2014. For each combination, we calculated adjusted observed-to-expected (O/E) ratios, using Co-Occurring Defect Analysis (CODA).

RESULTS:

Among 16,442 cases with hypospadias and without known syndromes, 2,084 (12.7%) had at least one additional defect. Many of the birth defect combinations within the highest adjusted O/E ratios included cardiac, musculoskeletal, and additional urogenital defects. For example, a top combination with an adjusted O/E of 139.0 included renal agenesis and dysgenesis, reduction defects of the upper limb, and other anomalies of upper limb (including shoulder girdle). High adjusted O/E ratios were also observed in combinations that included defects outside of the urogenital developmental field. For instance, the combination with the highest O/E ratio included buphthalmos, and congenital cataract and lens anomalies (adjusted O/E ratio 192.9). Similar results were obtained when we restricted our analyses to cases with second- or third-degree hypospadias.

DISCUSSION:

Many combinations in the top results were expected (e.g., multiple urogenital defects); however, some combinations with seemingly unrelated patterns of defects may suggest the presence of some etiologic mechanisms yet to be identified.

CONCLUSION:

In summary, this study described patterns of co-occurring defect combinations with hypospadias that can inform further study and may provide insights for screening and diagnostic practices.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Congenital Abnormalities / Hypospadias Type of study: Prevalence_studies / Risk_factors_studies Limits: Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: J Pediatr Urol Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Congenital Abnormalities / Hypospadias Type of study: Prevalence_studies / Risk_factors_studies Limits: Humans / Infant / Male Country/Region as subject: America do norte Language: En Journal: J Pediatr Urol Year: 2021 Type: Article Affiliation country: United States