Publication Detail
The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.
Serum alanine aminotransferase is correlated with hematocrit in healthy human subjects.
Yun Hu; Soren Snitker; Kathleen A Ryan; Rongze Yang; Braxton D Mitchell; Alan R Shuldiner; Dalong Zhu; Da-Wei Gong (Profiled Authors: Da-Wei Gong; Braxton D Mitchell Jr.; Alan R Shuldiner; Soren Snitker; Rong-Ze Yang)
Division of Endocrinology, Diabetes and Nutrition, Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
Scandinavian journal of clinical and laboratory investigation 2012;72(3):258-64.
BACKGROUND: Serum alanine aminotransferase (ALT) activity is a widely-used surrogate marker for liver injury. However, mild elevation of serum ALT is frequently observed in apparently healthy individuals, making it sometimes challenging to interpret whether this laboratory abnormality is medically benign or serious. To obtain a better understanding of the factors influencing ALT levels, we examined the relation between ALT and a number of anthropometric and biochemistry measurements in humans. METHODS: We assessed the associations of ALT with hematocrit (HCT) in 1,200 apparently healthy adults from an Amish population. Multivariate analyses were carried out to determine whether observed associations were independent of other factors known to modulate ALT and HCT, including body mass index (BMI) and sex. The correlation detected in the Amish was then replicated in an independent population sample (N = 9,842) from the National Health and Nutrition Examination Survey (NHANES) III. RESULTS: ALT levels were positively correlated with HCT (r = 0.33, p < 0.0001) in both Amish and NHANES III. The magnitude of association was unchanged after adjustment for BMI, but was reduced by age/sex adjustment to r = 0.18 (p < 0.0001) and r = 0.17 (p < 0.0001) in the Amish and NHANES populations, respectively. HCT accounts for about 3% of the population variation in ALT, which is smaller than the contributions of gender and BMI, but larger than individual blood pressure and cholesterol components. CONCLUSIONS: We observed a correlation between ALT and HCT, suggesting that HCT may be a newly identified modulator of ALT in humans.
2 Originating Grant
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1.
Shuldiner, Alan R
Pharmacogenomics of CVD risk Reduction
23 September 2005 - 31 August 2010
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
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2.
SHULDINER, ALAN R.
Mid-Atlantic Nutrition Obesity Research Center
15 September 2005 - 31 August 2015
NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
Scientific Context
This section shows information related to the publication - computed using the fingerprint of the publication - including related publications, related experts and related grants with fingerprints representing significant amounts of overlap between their fingerprint and this publication. The red dots indicate whether those experts or terms appear within the publication, thereby showing potential and actual connections.
Related Publications
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1.
2004Toni I Pollin; Wen-Chi Hsueh; Nanette I Steinle; Soren Snitker; Alan R Shuldiner; Braxton D Mitchell
A genome-wide scan of serum lipid levels in the Old Order Amish.
Atherosclerosis 2004;173(1):89-96. -
2.
2004Soren Snitker; Alan R Shuldiner
Medicine and science in sports and exercise 2004;36(8):1447; author reply 1448. -
3.
2006Elizabeth A Streeten; Daniel J McBride; Toni I Pollin; Kathy Ryan; Jay Shapiro; Sandy Ott; Braxton D Mitchell; Alan R Shuldiner; Jeffery R O'Connell
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2006;21(9):1433-42.
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