Key result
Pediatric GPD1 mutations linked to persistent hypertriglyceridemia in ~72% of cases, alongside hepatomegaly and progressive steatosis.
Why the study?
Mutations in the GPD1 gene are a rare cause of monogenic hypertriglyceridemia in childhood, prompting this detailed analysis of clinical, laboratory, and molecular characteristics of patients with biallelic variants.
GPD1 deficiency is a rare but significant cause of childhood hypertriglyceridemia, hepatomegaly, and hepatic steatosis that may persist and lead to liver fibrosis or cirrhosis.
Answers are grounded in this paper and cite their sources.
Prompts GPD1 testing in children with hepatomegaly and hypertriglyceridemia; extends genetic causes of progressive pediatric cirrhosis.
Background and Objectives Mutations in the GPD1 gene, which encodes glycerol‐3‐phosphate dehydrogenase 1 (GPD1), are a rare cause of monogenic hypertriglyceridemia (HTG) during childhood. This study is aimed at providing a detailed analysis of the clinical, laboratory, and molecular characteristics of all patients affected by biallelic GPD1 gene variants, including three cases from our center. Methods A literature search was conducted across the English MEDLINE, PubMed, and Embase databases from 1966 to 2023 for the studies that reported on GPD1 deficiency with confirmed GPD1 gene variants using the search words HTG and GPD1 gene. Results A total of 39 children (including three from our center) were identified with 15 pathogenic mutations in GPD1 reported in 14 articles from 5 ethnicities (15 Arabs, 14 Caucasians, 4 Chinese, 5 Indian/South Asian, and 1 Turkish): 8 missense variants (one compound heterozygous), 3 nonsense, 3 frameshifts, and 1 splicing. Three of the 15 variants likely originated from a common ancestor, “that is, founder in nature”: p.I119fs∗94 (Palestinian Arabs), p.Gly299Arg (Czech population), and p.Thr251Asnfs∗10 (Saudi Arabia). The median age at presentation was 9 months. All patients manifested hepatomegaly, elevated transaminases, and HTG. Nineteen patients underwent liver biopsy; all showed micro‐ and macrosteatosis, mild to moderate portal fibrosis in 58% (11 out of 19), and cirrhosis in the remaining eight cases (42%). Follow‐up data showed that HTG normalized in 28% of patients (11 out of 39) but persisted mildly in the remaining 72% (28 out of 39). Conclusion Mutations in the GPD1 gene should be considered in children with hepatomegaly, hepatic steatosis, and HTG. This study indicates that GPD1 deficiency may not be a transient or benign condition, as previously considered, due to the persistence of HTG and liver pathology in a significant proportion of cases. Identifying specific GPD1 variants may expedite targeted molecular analysis.
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Alharbi et al. (2026) studied this question. GPD1 gene mutations in children cause hepatomegaly, persistent hypertriglyceridemia in 72% of cases, and hepatic steatosis progressing to cirrhosis in 42% of biopsied patients.
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