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. 2021 Sep 30;10(11):R293–R304. doi: 10.1530/EC-21-0294

Table 2.

Results of meta-regression and subgroup analysis concerning the frequency of pheochromocytoma and/or paraganglioma (PPGL) among patients with von Hippel–Lindau disease (vHL) of all types.

Meta-regression Subgroup analysis
N studies N vHL OR (95% CI) P value Frequency (%, 95% CI) Q Cochran P value I²
Publication year 45 4263 1.04 (1.01–1.08) 0.013* a a a
Sample size 45 4263 1.00 (1.00–1.00) 0.818 a a a
% of males 24 648 1.01 (0.98–1.03) 0.554 a a a
Mean cohort age 9 444 1.05 (0.96–1.16) 0.300 a a a
Mean onset age of vHL 13 1863 0.98 (0.91–1.07) 0.697 a a a
Region 45 4263 0.802b
Europe 21 2148 c c 19.1 (14.5–24.9) <0.001 84.4%
Asia and Pacific 16 1116 0.97 (0.55–1.71) 0.923 18.5 (12.9–25.9) <0.001 76.7%
America 8 999 1.23 (0.62–2.44) 0.558 21.0 (11.4–35.3) <0.001 92.6%
Sampling method 45 4263 0.352b
Consecutive 19 3684 c c 20.5 (16.3–25.5) <0.001 90.1%
Convenience 11 178 1.22 (0.61–2.41) 0.576 22.4 (11.7–38.7) <0.001 69.4%
Not specified 15 401 0.72 (0.40–1.28) 0.261 15.3 (9.9–23.0) <0.001 61.2%
Diagnosis method 45 4263 0.888b
Included genetic testing/not specified 42 4086 c c 19.7 (16.1– 23.8) <0.001 85.0%
Clinical criteria only 3 177 0.93 (0.32–2.70) 0.888 27.7 (3.2–81.6) <0.001 91.8%

aNot performed, as this is a continuous variable; bOmnibus P  value for this variable; cReference category; *Statistically significant P  value.