Abstract:Objective. This study aimed to examine the relationship between serum alanine aminotransferase (ALT) and growth hormone (GH) in children and adolescents with short stature. Methods. In this retrospective cohort study, 670 Chinese children and adolescents with short stature were included, and 253 of them received recombinant human GH (rhGH) therapy. Anthropometric and biochemical indicators were measured. GH peak levels were assessed after provocation tests with L-dopa and insulin. The subjects were divided int… Show more
“…In addition, a negative correlation was found between GH peak and ALT in subjects with GH peak <5 ng/mL. This nding is consistent with reports by Ji et al, who found that the GH secretion levels in children and adolescents with short stature were signi cantly and negatively correlated with ALT and that recombinant human growth hormone (rhGH) therapy reduced ALT levels [22] .…”
Objective: This study aimed to investigate the relationship between systolic blood pressure (SBP) and alanine aminotransferase (ALT) in children and adolescents with short stature based on growth hormone peak (peak GH).Methods: In this study, 1151 patients diagnosed with short stature in the Shandong Growth and Developmental Disease Follow-up Study Cohort were included and anthropometric and biochemical parameters were measured. In accordance with the peak GH level in the growth hormone challenge test, all subjects were divided into three groups to determine the correlation between SBP and ALT in children and adolescents with schizophrenia: peak GH < 5 ng/mL, 5 ng/mL ≤ peak GH < 10 ng/mL and peak GH ≥ 10 ng/mL. Cross-sectional analysis of the correlation between SBP and ALT in children and adolescents with short stature.Result: The serum ALT levels in the GH peak <5 ng/mL and 5 ng/mL ≤GH < 10 ng/mL groups were elevated compared with those in the GH peak ≥10 ng/mL group. Univariate analysis showed a significant positive correlation between SBP and ALT in subjects with peak GH <5 ng/mL and 5 ng/mL ≤ peak GH < 10 ng/mL (P < 0.05). After adjusting for possible confounding factors, further smooth curve fitting found a nonlinear relationship between SBP and ALT. Further analysis of threshold effects showed that in the GH peak < 5 ng/mL group, the serum ALT levels increased with SBP when SBP reached 116 mmHg (β 0.35; 95% CI 0.04, 0.67; P = 0.029). In the 5 ng/mL ≤ GH < 10 ng/mL group, the serum ALT levels increased with SBP when SBP reached 106 mmHg (β 0.19; 95% CI 0.05, 0.34; P = 0.010). However, in subjects with peak GH <5 ng/mL and 5 ng/mL ≤ peak GH <10 ng/mL, no correlation was observed when the SBP levels does not reach the inflection point. The relationship between serum ALT levels and SBP was not significant in the GH peak ≥10 ng/mL group (β 0.05; 95% CI −0.02, 0.11; P = 0.140).Conclusion: The serum ALT levels in the GH peak < 5 ng/mL and 5 ng/mL ≤GH peak < 10 ng/mL groups were elevated compared with those in the GH peak ≥ 10 ng/mL group and a nonlinear relationship was found between SBP and ALT. When SBP reached the inflection point, the serum ALT levels were positively correlated with the increase in SBP. Future research is required to explore this relationship and mechanism.
“…In addition, a negative correlation was found between GH peak and ALT in subjects with GH peak <5 ng/mL. This nding is consistent with reports by Ji et al, who found that the GH secretion levels in children and adolescents with short stature were signi cantly and negatively correlated with ALT and that recombinant human growth hormone (rhGH) therapy reduced ALT levels [22] .…”
Objective: This study aimed to investigate the relationship between systolic blood pressure (SBP) and alanine aminotransferase (ALT) in children and adolescents with short stature based on growth hormone peak (peak GH).Methods: In this study, 1151 patients diagnosed with short stature in the Shandong Growth and Developmental Disease Follow-up Study Cohort were included and anthropometric and biochemical parameters were measured. In accordance with the peak GH level in the growth hormone challenge test, all subjects were divided into three groups to determine the correlation between SBP and ALT in children and adolescents with schizophrenia: peak GH < 5 ng/mL, 5 ng/mL ≤ peak GH < 10 ng/mL and peak GH ≥ 10 ng/mL. Cross-sectional analysis of the correlation between SBP and ALT in children and adolescents with short stature.Result: The serum ALT levels in the GH peak <5 ng/mL and 5 ng/mL ≤GH < 10 ng/mL groups were elevated compared with those in the GH peak ≥10 ng/mL group. Univariate analysis showed a significant positive correlation between SBP and ALT in subjects with peak GH <5 ng/mL and 5 ng/mL ≤ peak GH < 10 ng/mL (P < 0.05). After adjusting for possible confounding factors, further smooth curve fitting found a nonlinear relationship between SBP and ALT. Further analysis of threshold effects showed that in the GH peak < 5 ng/mL group, the serum ALT levels increased with SBP when SBP reached 116 mmHg (β 0.35; 95% CI 0.04, 0.67; P = 0.029). In the 5 ng/mL ≤ GH < 10 ng/mL group, the serum ALT levels increased with SBP when SBP reached 106 mmHg (β 0.19; 95% CI 0.05, 0.34; P = 0.010). However, in subjects with peak GH <5 ng/mL and 5 ng/mL ≤ peak GH <10 ng/mL, no correlation was observed when the SBP levels does not reach the inflection point. The relationship between serum ALT levels and SBP was not significant in the GH peak ≥10 ng/mL group (β 0.05; 95% CI −0.02, 0.11; P = 0.140).Conclusion: The serum ALT levels in the GH peak < 5 ng/mL and 5 ng/mL ≤GH peak < 10 ng/mL groups were elevated compared with those in the GH peak ≥ 10 ng/mL group and a nonlinear relationship was found between SBP and ALT. When SBP reached the inflection point, the serum ALT levels were positively correlated with the increase in SBP. Future research is required to explore this relationship and mechanism.
“…Skin diseases have been broadly described in postmenopausal women and correlate with letrozole‐induced changes in sex hormone levels 37 . Abnormal liver function has been observed in GH monotherapy patients; in the boy from this study, letrozole treatment was stopped, but he continued on GH after 15 days; liver function return to normal 38 . In prior studies, HDL‐C reductions within the normal range have been observed; here, four boys had HDL‐C reductions below the limit of 1.04 mmol/L 12 …”
Section: Discussionmentioning
confidence: 50%
“…37 Abnormal liver function has been observed in GH monotherapy patients; in the boy from this study, letrozole treatment was stopped, but he continued on GH after 15 days; liver function return to normal. 38 In prior studies, HDL-C reductions within the normal range have been observed; here, four boys had HDL-C reductions below the limit of 1.04 mmol/L. 12 ADRs should be closely monitored during letrozole therapy in Chinese pubertal boys.…”
Aims: Recently, letrozole has been used off-label to treat short pubertal boys. The experience on letrozole effectiveness and safety has been obtained primarily from Caucasian children. A simple extrapolation of the data to Chinese paediatric populations is questionable because of the substantial ethnic differences between the two populations. Therefore, the present study aimed to determine the effectiveness and safety of letrozole use in Chinese short pubertal boys as well as to establish an exposure-response relationship.Methods: Forty-one Chinese boys were included in the study. Patients were given letrozole tablets (2.5 mg) once daily in combination with growth hormone, and follow-up visits were made after 1, 3, 6 and 12 months of treatment. Plasma samples were taken from clinical examinations and analysed using high performance liquid chromatography with fluorescence detection.Results: After 1 year of treatment, 35 (88%) boys showed increased predicted adult heights. However, possible adverse drug reactions were seen in nine boys (22%).Predicted adult heights increased significantly from 168.4 ± 3.7 to 173.0 ± 4.2 cm, while oestrogen levels dropped from 33.2 ± 7.4 to 21.6 ± 7.3 pg/mL. Increments in predicted adult height were significantly correlated with trough letrozole concentrations (r = 0.39, P = .01).
Conclusion:Letrozole treatment in Chinese pubertal populations should be further optimized, and more personalized therapies should be developed.
“…Few studies have evaluated the presence of NAFLD in GHD children due to the very low prevalence of NAFLD in young children. A recent study reported a negative association between PGH level and ALT level in short children and adolescents without NAFLD [36].…”
This study investigated the relationship between the stimulated peak growth hormone (PGH) level and comprehensive metabolic markers for glucose and lipid metabolism, and liver steatosis in prepubertal children with GH deficiency (GHD). Methods: Sixty-nine prepubertal children with GHD were divided into overweight/obesity (body mass index [BMI]≥85th percentile) and normal BMI groups. The associations between PGH level and metabolic parameters including homeostatic model assessment-insulin resistance (HOMA-IR), lipid profiles, AST, and ALT were evaluated. Results: The LDL cholesterol level was significantly higher in the overweight/obesity group than in the normal BMI group. PGH level was negatively associated with the BMI SD score (SDS) (r= −0.26, P=0.029) and ALT (r=−0.36, P=0.004) levels, whereas it was positively associated with the HDL-cholesterol (HDL-C) level (r=0.38, P=0.002). In multivariate analyses, PGH level was positively associated with HDL-C level (P=0.002) and negatively associated with ALT level (P=0.028) after adjusting for age, sex, BMI SDS, HOMA-IR, and TG level. Conclusion: PGH level in pre-pubertal children with GHD was positively and negatively associated with HDL-C and ALT, respectively, even if they were within normal range, regardless of BMI.
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