14 research outputs found
Alcohol use among adolescents in India: a systematic review
Abstract
Background
Alcohol use is typically established during adolescence and initiation of use at a young age poses risks for short- and long-term health and social outcomes. However, there is limited understanding of the onset, progression and impact of alcohol use among adolescents in India. The aim of this review is to synthesise the evidence about prevalence, patterns and correlates of alcohol use and alcohol use disorders in adolescents from India.
Methods
Systematic review was conducted using relevant online databases, grey literature and unpublished data/outcomes from subject experts. Inclusion and exclusion criteria were developed and applied to screening rounds. Titles and abstracts were screened by two independent reviewers for eligibility, and then full texts were assessed for inclusion. Narrative synthesis of the eligible studies was conducted.
Results
Fifty-five peer-reviewed papers and one report were eligible for inclusion in this review. Prevalence of ever or lifetime alcohol consumption ranged from 3.9% to 69.8%; and prevalence of alcohol consumption at least once in the past year ranged from 10.6% to 32.9%. The mean age for initiation of drinking ranged from 14.4 to 18.3 years. Some correlates associated with alcohol consumption included being male, older age, academic difficulties, parental use of alcohol or tobacco, non-contact sexual abuse and perpetuation of violence.
Conclusion
The evidence base for alcohol use among adolescents in India needs a deeper exploration. Despite gaps in the evidence base, this synthesis provides a reasonable understanding of alcohol use among adolescents in India and can provide direction to policymakers.
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Sahoo-Supplement Fig 2.pdf
<p><b>Micro-architectural
parameters of iliac crest bone evaluated by µCT</b></p>
<p>(a)
3-D µCT images showing a normal bone and gross micro-architectural
deterioration in the proband’s bone, (b<b>)</b>
All parameters of cortical bone microarchitecture; T.Ar (periosteal area), B.Ar
(cortical mean cross-section area), Cs.Th (cortical thickness), T.Pm
(periosteal perimeter), and B.Pm (cortical bone perimeter) are significantly
lower in the proband compared to age and sex-matched healthy control,<b> </b>(c)<b> </b>Parameters of trabecular bone microarchitecture; Tb.Th (trabecular
thickness), and Tb.N (trabecular number) are decreased, while Tb.Sp (trabecular
separation) and SMI (structure model index) are increased in the proband’s
bone. All values are expressed as mean ± S.E. </p>
<p>*
p<0.05 and ** p<0. 01versus control</p
Supplementary Data File- Hypophosphataemic osteomalacia in a patient with neurofibromatosis type 1- a role for FGF23?
<h2>Supplementary Data File</h2
Supplementary Data-Hypophosphataemic osteomalacia in a patient with neurofibromatosis type 1- a role for FGF23?
Supplementary Dat
Supplement Figures - Hypophosphataemic osteomalacia in a patient with neurofibromatosis type 1- a role for FGF23?
<p><b>Supplement
Figure 1</b></p>
<p><b><i>Family pedigree</i> </b><br>
<b></b></p><p><br></p><p><br></p>
<p><b>Supplement Figure 2</b></p>
<p><b><i>Micro-architectural
parameters of iliac crest bone evaluated by µCT</i></b></p>
<p>(a)
3-D µCT images showing a normal bone and gross micro-architectural
deterioration in the proband’s bone, (b<b>)</b>
All parameters of cortical bone microarchitecture; T.Ar (periosteal area), B.Ar
(cortical mean cross-section area), Cs.Th (cortical thickness), T.Pm
(periosteal perimeter), and B.Pm (cortical bone perimeter) are significantly
lower in the proband compared to age and sex-matched healthy control,<b> </b>(c)<b> </b>Parameters of trabecular bone microarchitecture; Tb.Th (trabecular
thickness), and Tb.N (trabecular number) are decreased, while Tb.Sp (trabecular
separation) and SMI (structure model index) are increased in the proband’s
bone. All values are expressed as mean ± S.E. </p>
<p>*
p<0.05 and ** p<0. 01 versus control</p
Sahoo-Supplement Fig 1.Hypophosphataemic osteomalacia in a patient with neurofibromatosis type 1- a role for FGF23?
<b>Family pedigree </b