Study design
|
|
|
Case-Control (14 studies) |
41% (27–57) |
96.50% |
Cross-Sectional (13 studies) |
48% (33–63) |
98.14% |
Case-Series (6 studies) |
43% (20–60) |
94.54% |
Cohort (3 studies) |
31% (8–60) |
Not estimable |
Region
|
|
|
Asia (15 studies) |
42% (28–56) |
98.15% |
Europe (8 studies) |
48% (38–58) |
89.36% |
Latin America (6 studies) |
55% (35–75) |
93.41% |
USA and Canada (5 studies) |
30% (11–52) |
95.81% |
Africa (2 studies) |
45% (36–54) |
Not estimable |
NAFLD assessment method
|
|
|
Ultrasound (26 studies) |
46% (38–55) |
95.61% |
Transient elastography ( 4studies) |
46% (15–79) |
98.23% |
CT-Scan (2 studies) |
3% (0–11) |
Not estimable |
Non-invasive blood biomarkers/Panels (2 studies) |
55% (52–59) |
Not estimable |
MRI (1 study) |
46% (31–53) |
Not estimable |
PCOS diagnostic criteria
|
|
|
Rotterdam (31 studies) |
45% (36–54) |
97.52% |
NIH (4 studies) |
35% (17–57) |
89.09% |
AE and PCOS society (1 study) |
24% (16–33) |
Not estimable |
Part 2. Risk Factors Meta-analysis
|
Factor
|
Odds Ratio (95% CI)
|
Heterogeneity, I2
|
BMI (8 studies) |
1.35 (1.28–1.430) |
70.00% |
Waist circumference (5 studies) |
1.016 (1.006–1.027) |
71.60% |
ALT (4 studies) |
1.007 (1.001–1.014) |
81.40% |
HOMA -IR (4 studies) |
1.21 (1.09–1.24) |
36.50% |
HDL (2 studies) |
0.99 (0.96–1.03) |
72.10% |
Free Androgen Index (2 studies) |
1.06 (1.03–1.1) |
82.30% |
Hyperandrogenism (2 studies) |
10.3 (4.2–25.2) |
58.10% |
Triglycerides (2 studies) |
1.002 (1.001–1.004) |
63.60% |